Crystallography Open Database

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7132778 CIFC18 H14 Ca F9 N3 O8P 1 21/n 124.1213; 8.1633; 24.2668
90; 98.981; 90
4719.8Baudet, Judith; Lesur, Emilie; Ribéraud, Maxime; Chevalier, Arnaud; D'Anfray, Timothée; Thuéry, Pierre; Audisio, Davide; Taran, Frédéric
Synthesis of sydnonimines from sydnones and their use for bioorthogonal release of isocyanates in cells.
Chemical communications (Cambridge, England), 2024, 60, 3657-3660
7132779 CIFC36 H92 I2 K O10 Si8 UP -113.4213; 15.8641; 16.3965
104.442; 102.934; 96.066
3246.4Lin, Nathan J.; Zeller, Matthias; Bart, Suzanne C.
Solution and solid-state characterization of rare silyluranium(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3954-3957
7132780 CIFC36 H98 I2 K O11 Si8 UP 1 2/c 114.8717; 15.8095; 28.9025
90; 103.785; 90
6599.7Lin, Nathan J.; Zeller, Matthias; Bart, Suzanne C.
Solution and solid-state characterization of rare silyluranium(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3954-3957
7132781 CIFC40 H98 I2 K O10 Si8 UC 1 2/c 149.049; 13.108; 21.124
90; 90.054; 90
13581Lin, Nathan J.; Zeller, Matthias; Bart, Suzanne C.
Solution and solid-state characterization of rare silyluranium(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3954-3957
7132782 CIFC27 H15 B F N5P -18.0536; 8.9238; 15.0934
79.306; 85.035; 65.599
970.63Kage, Yuto; Jiang, Yuchuan; Minakuchi, Namiki; Mori, Shigeki; Shimizu, Soji
One-pot synthesis of azabora[6]helicene by a Schiff base forming reaction.
Chemical communications (Cambridge, England), 2024, 60, 3543-3546
7132783 CIFC34 H22 B Cl2 N5P -19.3419; 10.0645; 14.7904
91.141; 105.751; 90.019
1338.11Kage, Yuto; Jiang, Yuchuan; Minakuchi, Namiki; Mori, Shigeki; Shimizu, Soji
One-pot synthesis of azabora[6]helicene by a Schiff base forming reaction.
Chemical communications (Cambridge, England), 2024, 60, 3543-3546
7132784 CIFC16 H13 F2 N OP 1 21/n 110.169; 10.856; 12.0502
90; 102.79; 90
1297.27Wang, Xuan; Li, Jianlong; Du, Haifang; Liang, Weihong; Luo, Cheng; Wu, Yunshan; Liu, Bo
Synthesis of 1,4-epoxy-2-aryltetrahydro-1-benzazepines <i>via</i> rhodium(III)-catalyzed C-H allylation/intramolecular 1,3-dipolar cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 2401-2404
7132785 CIFC16 H13 F2 N OP -19.7065; 11.7198; 12.029
77.71; 89.322; 71.433
1265.13Wang, Xuan; Li, Jianlong; Du, Haifang; Liang, Weihong; Luo, Cheng; Wu, Yunshan; Liu, Bo
Synthesis of 1,4-epoxy-2-aryltetrahydro-1-benzazepines <i>via</i> rhodium(III)-catalyzed C-H allylation/intramolecular 1,3-dipolar cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 2401-2404
7132786 CIFC210 H228 Ag3 B F4 N36 O24R 3 2 :H38.1751; 38.1751; 37.5163
90; 90; 120
47349Bajpayee, Nikhil; Pophali, Salil; Vijayakanth, Thangavel; Nandi, Shyamapada; Desai, Aamod V.; Kumar, Vinod; Jain, Rahul; Bera, Santu; Shimon, Linda J. W.; Misra, Rajkumar
Metal-driven folding and assembly of a minimal β-sheet into a 3D-porous honeycomb framework.
Chemical communications (Cambridge, England), 2024, 60, 2621-2624
7132787 CIFC76 H65 Cu2 N20 O16.5P 4319.7601; 19.7601; 19.9303
90; 90; 90
7782Qiu, Zhao-Feng; Wang, Peng; Zhang, Xiao-Yu; Chen, Jia-Qi; Zhang, Kai-Yang; Lu, Xiang-Yu; Zhao, Yue; Sun, Wei-Yin
Supramolecular assemblies of Cu(II) with a tetraphenylethene-imidazole ligand for tuning photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 2204-2207
7132788 CIFC40 H33 Cl4 Cu2 N9 OP 1 21/n 115.805; 9.323; 27.137
90; 99.835; 90
3939.9Qiu, Zhao-Feng; Wang, Peng; Zhang, Xiao-Yu; Chen, Jia-Qi; Zhang, Kai-Yang; Lu, Xiang-Yu; Zhao, Yue; Sun, Wei-Yin
Supramolecular assemblies of Cu(II) with a tetraphenylethene-imidazole ligand for tuning photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 2204-2207
7132789 CIFC41.5 H45.5 N6.5 O18 Tb TiP m -3 n25.9298; 25.9298; 25.9298
90; 90; 90
17434Yao, Qingxia; Pan, Xuze; Si, Xuezhen; Wang, Xin; Zhang, Xiaoying; Hou, Jinle; Su, Jie; Qiu, Yi; Li, Jun
A porous and photoactive Ti-MOF based on a novel tetranuclear [Ti<sub>2</sub>Tb<sub>2</sub>] cluster.
Chemical communications (Cambridge, England), 2024, 60, 2188-2191
7132790 CIFC29 H32 N2 O5P -111.4759; 11.5363; 19.7187
85.779; 79.152; 85.444
2551.2Lai, Jingxiong; Huang, You
A highly diastereoselective (5+1) annulation of allenoates and pyrazolones catalyzed by CH<sub>3</sub>OK.
Chemical communications (Cambridge, England), 2024, 60, 2066-2069
7132791 CIFC10 H19 N O3P 1 21 15.4153; 11.2753; 9.4479
90; 98.633; 90
570.34Zhang, Qiuxin; Zhang, Heng; Geng, Senbai; Zhao, Xian; Liu, Shucheng; Hong, Kun; Pan, Jianming; Yan, Xingchen
Green transformation of CO<sub>2</sub> into γ-amino alcohols with continuous stereocenters.
Chemical communications (Cambridge, England), 2024, 60, 2062-2065
7132792 CIFC52 H52 B2 Hg N14 O4 Se2 W2P -113.7335; 21.8752; 22.673
117.984; 91.487; 103.84
5764.1Onn, Chee S.; Hill, Anthony F.; Ward, Jas S.
Spodium bonding in bis(alkynyl)mecurials.
Chemical communications (Cambridge, England), 2024, 60, 2552-2555
7132793 CIFC20 H23 B N6 O2 Se WP 1 21/c 17.9715; 18.2689; 19.7379
90; 101.415; 90
2817.58Onn, Chee S.; Hill, Anthony F.; Ward, Jas S.
Spodium bonding in bis(alkynyl)mecurials.
Chemical communications (Cambridge, England), 2024, 60, 2552-2555
7132794 CIFC29 H43 B N6 O2 Si Te WP -110.6281; 11.0432; 15.1354
84.687; 87.521; 75.938
1715.38Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132795 CIFC21 H30 Au B Cl6 N6 O2 S Te WP -111.1523; 11.161; 14.3505
89.093; 89.186; 77.275
1742.02Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132796 CIFC64 H100 B2 Cl4 Cu4 N12 O4 Si2 Te2 W2P 1 21/n 110.9539; 18.7716; 20.4333
90; 102.63; 90
4099.87Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132797 CIFC24 H27 B N8 O2 Te WP 1 21 17.9095; 18.2594; 9.7522
90; 99.742; 90
1388.13Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132798 CIFC23 H31 Au B Cl N6 O2 S Si WP 1 21/m 112.3181; 24.9472; 16.5061
90; 108.592; 90
4807.6Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132799 CIFC26 H27 B N6 O2 Te WP 1 21/n 120.5319; 14.2779; 21.6073
90; 117.804; 90
5602.9Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132800 CIFC33 H28 F3 N3 O2P 21 21 218.2405; 13.6044; 25.8384
90; 90; 90
2896.67Wang, Lan; Lu, Mengxi; Li, Kuan; Yang, Sen; Wang, Lei; Guo, Hongchao
Palladium-catalyzed enantioselective umpolung allylation of amido-tethered allylic carbonates with isatin-derived ketimines.
Chemical communications (Cambridge, England), 2024, 60, 3729-3732
7132801 CIFC22 H17 F N2P 1 21/c 16.2418; 18.1094; 15.2988
90; 96.701; 90
1717.49Qin, Jiaze; Jiang, Shixuan; Luo, Xiaofeng; Wang, Tianqiang; Liu, Peihua; Yuan, Bingxiang; Yan, Rulong
I<sub>2</sub>-catalyzed synthesis of 3-aminopyrrole with homopropargylic amines and nitrosoarenes.
Chemical communications (Cambridge, England), 2024, 60, 3701-3704
7132802 CIFC38 H28 N8P 1 21/n 111.5521; 9.4107; 32.526
90; 95.722; 90
3518.39Zhang, Li; Luo, Yu-Ting; Xiao, Sai-Jin; Fan, Jia-Qi; Tan, Quan-Gen; Sun, Chen; Song, An-Min; Liang, Ru-Ping; Qiu, Jian-Ding
The construction of a stable hydrogen-bonded organic framework for the photocatalytic reduction and removal of uranium.
Chemical communications (Cambridge, England), 2024, 60, 3583-3586
7132803 CIFC19 H17 Br O2P 21 21 217.1586; 11.9651; 18.845
90; 90; 90
1614.1Li, Zheyao; Zhang, Huiwen; Zhao, Lin; Ma, Yueyue; Wu, Qiufang; Ren, Haosong; Lin, Zhongren; Zheng, Jun; Yu, Xinhong
Metal-free β,γ-C(sp<sup>3</sup>)-H difunctionalization of propanols: DMP-initiated asymmetric spirocyclopropanation.
Chemical communications (Cambridge, England), 2024, 60, 3579-3582
7132804 CIFC29 H19 N O5P -19.9434; 11.2111; 11.3362
100.833; 92.317; 115.863
1106.1Wang, Kai-Kai; Li, Yan-Li; Li, Ya-Fei; Yao, Wei-Wei; Li, Lan-Xin; He, Xiao-Long; Chen, Rongxiang
Substrate-controlled [4+1] and [3+2] annulations of ninhydrin-derived Morita-Baylis-Hillman carbonates to access polysubstituted furans and cyclopentenes.
Chemical communications (Cambridge, England), 2024, 60, 3717-3720
7132805 CIFC29 H18 O6P 1 21/c 18.5559; 26.5; 9.988
90; 99.097; 90
2236.1Wang, Kai-Kai; Li, Yan-Li; Li, Ya-Fei; Yao, Wei-Wei; Li, Lan-Xin; He, Xiao-Long; Chen, Rongxiang
Substrate-controlled [4+1] and [3+2] annulations of ninhydrin-derived Morita-Baylis-Hillman carbonates to access polysubstituted furans and cyclopentenes.
Chemical communications (Cambridge, England), 2024, 60, 3717-3720
7132806 CIFC27 H23 NP 1 21/n 19.4988; 11.9651; 17.3667
90; 97.139; 90
1958.49Shinde, Jivan; Suresh, Sundaram; Kavala, Veerababurao; Yao, Ching-Fa
Pd(II)-catalyzed hydroarylations/hydroalkenylations of terminal alkynes: regioselective synthesis of allylic, homoallylic, and 1,3-diene systems.
Chemical communications (Cambridge, England), 2024, 60, 3790-3793
7132807 CIFC16 H14 O2P n a 2116.5657; 5.4295; 14.0697
90; 90; 90
1265.48Shinde, Jivan; Suresh, Sundaram; Kavala, Veerababurao; Yao, Ching-Fa
Pd(II)-catalyzed hydroarylations/hydroalkenylations of terminal alkynes: regioselective synthesis of allylic, homoallylic, and 1,3-diene systems.
Chemical communications (Cambridge, England), 2024, 60, 3790-3793
7132808 CIFC26 H23.62 Cl0.38 N2 O3 SP 1 21/n 110.908; 15.648; 14.141
90; 112.321; 90
2232.8Wang, Bi; Liang, Ren-Xiao; Shen, Zhen-Lu; Jia, Yi-Xia
Copper-catalyzed intramolecular dearomative aza-Wacker reaction of indole.
Chemical communications (Cambridge, England), 2024, 60, 3858-3861
7132809 CIFC20 H22 O2P 1 21 18.546; 6.518; 15.6
90; 105.428; 90
837.7Magham, Lakshmi Revati; Samad, Abdus; Thopate, Satish B.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
Organocatalytic enantioselective desymmetrization of enal-tethered cyclohexane-1,3-diones.
Chemical communications (Cambridge, England), 2024, 60, 3834-3837
7132810 CIFC18 H20 Cl N O2P -18.3513; 13.4596; 15.583
77.965; 76.1; 77.207
1635.64Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132811 CIFC18 H17 Cl F3 N OP 1 21/c 16.2156; 11.1571; 24.7517
90; 92.551; 90
1714.78Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132812 CIFC17 H24 Cl N OP 1 21/n 19.2235; 7.0079; 25.1221
90; 94.528; 90
1618.76Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132813 CIFC14 H18 Cl N OI 1 2/a 118.5653; 6.3699; 23.6434
90; 108.817; 90
2646.61Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132814 CIFC19 H22 Cl N OP 1 21/n 116.7373; 6.1891; 18.0916
90; 110.509; 90
1755.3Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132815 CIFC15 H20 Cl N OC 1 2/c 117.0047; 6.656; 24.757
90; 92.075; 90
2800.24Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132816 CIFC16 H22 Cl N OP 1 21/c 112.6132; 6.8258; 17.3255
90; 93.319; 90
1489.14Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132817 CIFC17 H18 Cl N OP 21 21 217.6345; 9.6295; 20.4737
90; 90; 90
1505.15Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132818 CIFC13 H18 Cl N OP -16.66649; 9.4285; 10.2117
93.58; 96.362; 93.083
635.47Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132819 CIFC26 H44 B N2 SiP -110.212; 11.708; 12.522
106.885; 100.518; 90.377
1405.7Wang, Hanqiang
Synthesis, structure and reactivity of iminoborane radicals.
Chemical communications (Cambridge, England), 2024, 60, 3806-3809
7132820 CIFC35 H62 B N3 O SiP 1 21/n 110.2572; 18.663; 19.5822
90; 99.642; 90
3695.67Wang, Hanqiang
Synthesis, structure and reactivity of iminoborane radicals.
Chemical communications (Cambridge, England), 2024, 60, 3806-3809
7132821 CIFC66 H96 B2 N4 O2 Si2C 1 2/c 116.1834; 30.376; 17.5363
90; 113.974; 90
7876.9Wang, Hanqiang
Synthesis, structure and reactivity of iminoborane radicals.
Chemical communications (Cambridge, England), 2024, 60, 3806-3809
7132822 CIFC20 H15 Cl3 O2P 1 21/c 110.8147; 9.8903; 16.969
90; 104.319; 90
1758.6Zhou, Hongxun; Li, Lijun; Yan, Qinqin; Ma, Jinyue; Wang, Ying; Gao, Yongjun; Liu, Zhong-Quan; Li, Zejiang
Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes.
Chemical communications (Cambridge, England), 2024, 60, 3938-3941
7132823 CIFC24 H16 O2P 1 21/c 112.2366; 17.3994; 8.2782
90; 102.186; 90
1722.8Zhou, Hongxun; Li, Lijun; Yan, Qinqin; Ma, Jinyue; Wang, Ying; Gao, Yongjun; Liu, Zhong-Quan; Li, Zejiang
Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes.
Chemical communications (Cambridge, England), 2024, 60, 3938-3941
7132824 CIFC19 H15 Cl OP -19.6677; 12.9019; 13.3368
73.28; 88.509; 71.049
1502.7Zhou, Hongxun; Li, Lijun; Yan, Qinqin; Ma, Jinyue; Wang, Ying; Gao, Yongjun; Liu, Zhong-Quan; Li, Zejiang
Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes.
Chemical communications (Cambridge, England), 2024, 60, 3938-3941
7132825 CIFC12 H11 Br2 N3 ZnP -17.8069; 7.8757; 11.9902
77.783; 85.879; 77.735
703.79Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132826 CIFC14 H17 Br2 N3 S ZnP -17.852; 10.8828; 11.3769
75.796; 74.568; 76.283
892.99Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132827 CIFC15 H19 Br2 N3 O S ZnP -17.5172; 10.647; 13.487
105.076; 92.008; 109.849
971.3Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132828 CIFC15 H17 Br2 N3 O S ZnP 1 21/c 17.3412; 19.033; 13.475
90; 98.398; 90
1862.6Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132829 CIFC26 H26 Cl N3 O5P -18.2719; 10.9748; 14.3779
91.073; 98.225; 110.945
1203Li, Ming-Jun; Lu, Ming-Ming; Xu, Peng; Chen, Si-Qi; Wu, Luan-Ting; Zhang, Ze; Xu, Hui
Chemodivergent mechanosynthesis of cyclopentenyl and pyrrolinyl spirobarbiturates from unsaturated barbiturates and enamino esters.
Chemical communications (Cambridge, England), 2024, 60, 3958-3961
7132830 CIFC28.01 H30.01 Br N3 O5P -111.0881; 11.9277; 12.1514
115.124; 105.133; 100.196
1326.22Li, Ming-Jun; Lu, Ming-Ming; Xu, Peng; Chen, Si-Qi; Wu, Luan-Ting; Zhang, Ze; Xu, Hui
Chemodivergent mechanosynthesis of cyclopentenyl and pyrrolinyl spirobarbiturates from unsaturated barbiturates and enamino esters.
Chemical communications (Cambridge, England), 2024, 60, 3958-3961
7132831 CIFC98 H72 Cl4 Cu2 F20 N8P 1 21/c 117.46; 22.68; 14.222
90; 95.69; 90
5604Dong, Yuting; Qian, Long; Chen, Feng; Wang, Yue; Zhang, Tao; Qiu, Fengxian; Teranishi, Toshiharu; Xue, Songlin
Benzene-fused porphyrin(2.1.2.1) array: synthesis, structure, and electrocatalytic hydrogen evolution.
Chemical communications (Cambridge, England), 2024, 60, 3986-3989
7132832 CIFC19 H17 F3 N2 O4 SP b c a19.2019; 13.9245; 28.2926
90; 90; 90
7564.8Lou, Mingliang; Liu, Xiaolei; Han, Shoule; Bai, Songlin; Qi, Xiangbing
Total synthesis of (±)-3-demethoxyerythratidinone <i>via</i> Tf<sub>2</sub>O-promoted cascade reaction of enaminone.
Chemical communications (Cambridge, England), 2024, 60, 3842-3845
7132833 CIFC18 H17 F3 N2 O4 SP b c a19.421; 13.8099; 27.8614
90; 90; 90
7472.49Lou, Mingliang; Liu, Xiaolei; Han, Shoule; Bai, Songlin; Qi, Xiangbing
Total synthesis of (±)-3-demethoxyerythratidinone <i>via</i> Tf<sub>2</sub>O-promoted cascade reaction of enaminone.
Chemical communications (Cambridge, England), 2024, 60, 3842-3845
7132834 CIFC20 H18 N2 O4.5 VP 1 21/c 115.3045; 8.8087; 13.3399
90; 98.687; 90
1777.76Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132835 CIFC55.66 H21.3 Cl3.31 F10 N8 Pd SP 1 21 113.3831; 7.1785; 26.0801
90; 93.166; 90
2501.71Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132836 CIFC45 H29 B Cl3 F4 N3 Pd SP -19.276; 14.42; 15.664
112.75; 91.73; 91.28
1930Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132837 CIFC74 H42 B F20 N3 Pd SP 1 21/n 113.546; 27.1678; 16.8019
90; 99.633; 90
6096.17Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132838 CIFC46 H32 Cl4 F6 N3 P Pd SP 1 21/c 113.77; 16.0819; 19.035
90; 90.479; 90
4215.1Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132839 CIFC55 H29 Cl3 N8 Pd SP -114.7468; 17.6065; 20.521
69.671; 82.618; 65.328
4539.2Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132840 CIFC47 H20.5 Cl0.5 F16 N3 P Pd SP n a 2128.14; 14.513; 20.554
90; 90; 90
8394Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132841 CIFC20 H26 O4I 1 2/a 110.1083; 14.7871; 22.9034
90; 91.199; 90
3422.68Koyama, Ryosei; Anada, Masahiro; Sueki, Shunsuke; Makino, Kosho; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Divergent synthesis of multi-substituted phenanthrenes <i>via</i> an internal redox reaction/ring expansion sequence.
Chemical communications (Cambridge, England), 2024, 60, 3822-3825
7132842 CIFC18 H24 O2P -19.864; 9.8656; 16.5931
105.165; 97.065; 105.295
1471Koyama, Ryosei; Anada, Masahiro; Sueki, Shunsuke; Makino, Kosho; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Divergent synthesis of multi-substituted phenanthrenes <i>via</i> an internal redox reaction/ring expansion sequence.
Chemical communications (Cambridge, England), 2024, 60, 3822-3825
7132843 CIFC27 H15 Br O2P 1 21/c 117.7637; 15.582; 7.0233
90; 95.518; 90
1935Nishimoto, Mikey; Uetake, Yuta; Yakiyama, Yumi; Sakurai, Hidehiro
Strain-induced carbon-carbon bond cleavage of bowl-shaped sumanenone.
Chemical communications (Cambridge, England), 2024, 60, 3982-3985
7132844 CIFC14 H11 N3 O2P 21 21 218.1213; 11.1938; 13.6325
90; 90; 90
1239.31Bhattacharjee, Suvam; Hajra, Alakananda
Site-selective direct nitration of 2<i>H</i>-indazoles: easy access to 7-nitroindazoles.
Chemical communications (Cambridge, England), 2024, 60, 4076-4079
7132845 CIFC38 H61 N4 P2 Sc SiP 1 21/c 115.5452; 15.3097; 17.8477
90; 97.496; 90
4211.3Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132846 CIFC73 H110 N10 Ni2 P4 Sc2P -112.49; 12.54; 13.517
65.861; 73.439; 76.945
1837.3Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132847 CIFC46 H59 N6 Ni P2 ScP -110.9882; 11.7463; 18.988
74.157; 89.563; 72.84
2245.6Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132848 CIFC43 H57 N4 Ni P2 ScP -111.122; 11.696; 16.447
101.88; 96.172; 90.996
2079.8Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132849 CIFC48 H68 N5 Ni O1.5 P2 ScP -110.142; 10.213; 23.78
77.96; 79.02; 81.49
2350Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132850 CIFC118 H142 N10 Ni2 O2 P4 Sc2C 1 2/c 128.918; 11.542; 36.001
90; 109.45; 90
11330Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132851 CIFC43 H58 N5 Ni P2 ScP -112.237; 13.83; 15.21
68.64; 72.04; 64.89
2134Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132852 CIFC21 H19 N O2P 1 21/c 110.0187; 15.8815; 10.6953
90; 99.728; 90
1677.28Karjee, Pallab; Debnath, Bijoy; Mandal, Santu; Saha, Sharajit; Punniyamurthy, Tharmalingam
One-pot C-N/C-C bond formation and oxidation of donor-acceptor cyclopropanes with tetrahydroisoquinolines: access to benzo-fused indolizines.
Chemical communications (Cambridge, England), 2024, 60, 4068-4071
7132853 CIFC22 H20 O5P 1 21/n 19.08906; 9.90544; 20.1477
90; 92.251; 90
1812.52Nambu, Hisanori; Onuki, Yuta; Aso, Kana; Kanamori, Momoka; Tomohara, Keisuke; Tsuge, Kiyoshi; Yakura, Takayuki
Ring expansion of spirocyclopropanes with stabilized sulfonium ylides: highly diastereoselective synthesis of cyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 4537-4540
7132854 CIFC21 H14 O2P 1 21/c 18.1483; 18.778; 9.9744
90; 98.77; 90
1508.3Gopalakrishnan, Dinesh Kumar; Bhardwaj, Srashti; Kumar, Sandeep; Karmakar, Tarak; Vaitla, Janakiram
Carbene-mediated stereoselective olefination of vinyl sulfoxonium ylides with diazo compounds and acetals.
Chemical communications (Cambridge, England), 2024, 60, 3846-3849
7132855 CIFC21 H18 O4P -18.487; 10.1115; 10.5324
91.975; 93.296; 108.179
856.01Gopalakrishnan, Dinesh Kumar; Bhardwaj, Srashti; Kumar, Sandeep; Karmakar, Tarak; Vaitla, Janakiram
Carbene-mediated stereoselective olefination of vinyl sulfoxonium ylides with diazo compounds and acetals.
Chemical communications (Cambridge, England), 2024, 60, 3846-3849
7132856 CIFC27 H50 Mn3 N6 O53 P W9P 3 1 c18.9481; 18.9481; 29.4882
90; 90; 120
9168.8Liu, Fangcheng; Han, Shicheng; Dong, Liwei; Fang, Xikui
Functionalized polyoxometalates enable fast ion transport in solid-state batteries at room temperature.
Chemical communications (Cambridge, England), 2024, 60, 4198-4201
7132857 CIFC17 H18 OP 1 21 111.5667; 5.2499; 12.1291
90; 117.369; 90
654.08Wang, Kun; Niu, Saisai; Tang, Weijun; Xue, Dong; Xiao, Jianliang; Li, Hongfeng; Wang, Chao
Ru-catalyzed asymmetric hydrogenation of α,β-unsaturated ketones <i>via</i> a hydrogenation/isomerization cascade.
Chemical communications (Cambridge, England), 2024, 60, 4338-4341
7132858 CIFC30 H45 F5 O2P 1 21 112.4586; 9.2797; 13.4386
90; 105.661; 90
1495.99Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132859 CIFC31 H45 F7 O2P 1 21 112.9607; 8.8159; 13.5926
90; 106.421; 90
1489.74Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132860 CIFC32 H45 F9 O2P 1 21 112.299; 9.2607; 14.5611
90; 94.027; 90
1654.38Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132861 CIFC31 H45 F7 O2P 1 21 112.7803; 9.3254; 13.7005
90; 104.745; 90
1579.07Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132862 CIFC33 H45 F11 O2P 21 21 219.236; 12.542; 29.3792
90; 90; 90
3403.2Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132863 CIFC34 H45 F13 O2P 1 21 113.3455; 8.8735; 14.404
90; 90.499; 90
1705.68Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132864 CIFC44 H53 Ca I N2 O2P 1 21/c 111.1453; 21.6411; 16.4519
90; 99.62; 90
3912.34Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132865 CIFC44 H53 I N2 O2 SrP 1 21/c 111.1365; 21.9592; 16.4408
90; 99.267; 90
3968.1Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132866 CIFC40 H57 N3 O Si2 SrC 1 2/c 122.9542; 9.945; 37.2321
90; 105.936; 90
8172.69Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132867 CIFC35.99 H48.98 Ca N3 Si2C 1 2/c 121.9451; 9.6032; 35.7576
90; 105.893; 90
7247.62Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132868 CIFC88 H64 N16 Pt2C 1 2/m 114.2019; 21.4417; 19.1515
90; 98.888; 90
5761.9van Hilst, Quinn V. C.; Pearcy, Aston C.; Preston, Dan; Wright, L. James; Hartinger, Christian G.; Brooks, Heather J. L.; Crowley, James D.
A dynamic covalent approach to [Pt<sub><i>n</i></sub>L<sub>2<i>n</i></sub>]<sup>2<i>n</i>+</sup> cages.
Chemical communications (Cambridge, England), 2024, 60, 4302-4305
7132869 CIFC100 H80 B4 F16 N16 Pt2P -111.1598; 14.8934; 17.8869
87.192; 75.514; 86.266
2870.67van Hilst, Quinn V. C.; Pearcy, Aston C.; Preston, Dan; Wright, L. James; Hartinger, Christian G.; Brooks, Heather J. L.; Crowley, James D.
A dynamic covalent approach to [Pt<sub><i>n</i></sub>L<sub>2<i>n</i></sub>]<sup>2<i>n</i>+</sup> cages.
Chemical communications (Cambridge, England), 2024, 60, 4302-4305
7132870 CIFC19 H17 Cl N2 O4P -19.6699; 9.6753; 10.4512
76.908; 71.347; 71.318
869.2Porashar, Bikoshita; Behera, Bipin Kumar; Phukon, Hunmoina; Saikia, Anil K.
Synthesis of tetrahydroquinazolines from 2-aminobenzonitriles and alkylidene malonates <i>via</i> 1,4-conjugate addition and an unprecedented rearrangement reaction.
Chemical communications (Cambridge, England), 2024, 60, 4358-4361
7132871 CIFC52 H34.66 Au3 Lu N20 O9.33P b c a19.9815; 23.8662; 23.8919
90; 90; 90
11393.6Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132872 CIFC52 H34.34 Au3 N20 O9.17 TbP b c a20.0668; 23.8472; 23.9197
90; 90; 90
11446.5Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132873 CIFC52 H34.51 Au3 Eu N20 O9.25P b c a20.1041; 23.8591; 23.936
90; 90; 90
11481.3Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132874 CIFC52 H34.4 Au3 Ce N20 O9.2P b c a20.2203; 23.8559; 23.9799
90; 90; 90
11567.3Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132875 CIFC19 H16 O4P 1 21/c 110.9362; 17.792; 8.2146
90; 108.127; 90
1519.04Zhou, Xinlong; Jiang, Jingjing; Zhang, Min; Wu, Qingqing; Zhu, Keyong; Shi, Dongjie; Hou, Sensen; Zhao, Jingjing; Li, Pan
Dioxane promoted photochemical <i>O</i>-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C-H and C-C bonds.
Chemical communications (Cambridge, England), 2024, 60, 4330-4333
7132876 CIFC20 H22 O5 SC 1 2/c 121.549; 10.8252; 17.856
90; 113.929; 90
3807.3Zhou, Xinlong; Jiang, Jingjing; Zhang, Min; Wu, Qingqing; Zhu, Keyong; Shi, Dongjie; Hou, Sensen; Zhao, Jingjing; Li, Pan
Dioxane promoted photochemical <i>O</i>-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C-H and C-C bonds.
Chemical communications (Cambridge, England), 2024, 60, 4330-4333
7132877 CIFC25 H22 O4P 1 21/c 110.2833; 10.038; 20.688
90; 98.406; 90
2112.6Zhou, Xinlong; Jiang, Jingjing; Zhang, Min; Wu, Qingqing; Zhu, Keyong; Shi, Dongjie; Hou, Sensen; Zhao, Jingjing; Li, Pan
Dioxane promoted photochemical <i>O</i>-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C-H and C-C bonds.
Chemical communications (Cambridge, England), 2024, 60, 4330-4333
7132878 CIFC16 H19 N O4P 1 21/n 113.824; 7.5535; 14.7562
90; 100.354; 90
1515.75Feng, Shishen; Liu, Hong; Li, Yan; Fang, Yewen
Photoredox-catalyzed radical-radical cross coupling of ketyl radicals with unstabilized primary alkyl radicals.
Chemical communications (Cambridge, England), 2024, 60, 4431-4434
7132879 CIFC57 H43 Au Br Cl18 Fe N6 OC m m m20.0212; 28.7967; 16.6677
90; 90; 90
9609.7Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132880 CIFC57 H43 Au Br Cl18 Fe N6 OP m m m10.4824; 14.6177; 17.0399
90; 90; 90
2611Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132881 CIFC88 H140 Co Fe N17 O19P m m m10.218; 14.6762; 17.0726
90; 90; 90
2560.2Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132882 CIFC83 H118 Fe2 N16 O15C m m m19.818; 29.05; 16.4847
90; 90; 90
9490.5Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132883 CIFC83 H118 Fe2 N16 O15C m m m20.623; 29.23; 17.01
90; 90; 90
10253.8Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132884 CIFC18 H13 N O3P b c a11.248; 11.9893; 21.1722
90; 90; 90
2855.19Liao, Zhi-Yu; Gao, Fan; Ye, Yu-Hang; Yu, Qian-Hui; Yang, Cui; Luo, Qing-Yu; Du, Fei; Pan, Bin; Zhong, Wen-Wu; Liang, Wu
Construction of cyclobutane-fused tetracyclic skeletons <i>via</i> substrate-dependent EnT-enabled dearomative [2+2] cycloaddition of benzofurans (benzothiophenes)/maleimides.
Chemical communications (Cambridge, England), 2024, 60, 4455-4458
7132885 CIFC21 H23 N O3 SP 1 21 110.5669; 8.0829; 11.7127
90; 113; 90
920.87Li, Hongye; Zhou, Yuqiao; Tan, Zheng; Wang, Xiangyu; Zhang, Yuxin; Wang, Fei; Feng, Xiaoming; Liu, Xiaohua
Enantioselective sulfonylation to construct 3-sulfonylated oxindoles.
Chemical communications (Cambridge, England), 2024, 60, 4354-4357
7132886 CIFC20 H16 Br N OP 1 21/c 110.887; 13.619; 11.857
90; 110.116; 90
1650.8Solanke, Pooja R.; Kumar, Prakash; Mainkar, Prathama S.; Nayani, Kiranmai; Chandrasekhar, Srivari
Synthesis of <i>cis</i>-fused cyclopentenone-pyrrolidine scaffolds <i>via</i> sequential aza-Piancatelli and Conia-ene type reactions in one pot.
Chemical communications (Cambridge, England), 2024, 60, 4234-4237
7132887 CIFC26 H21 N OP 1 n 18.577; 16.525; 29.33
90; 98.477; 90
4112Solanke, Pooja R.; Kumar, Prakash; Mainkar, Prathama S.; Nayani, Kiranmai; Chandrasekhar, Srivari
Synthesis of <i>cis</i>-fused cyclopentenone-pyrrolidine scaffolds <i>via</i> sequential aza-Piancatelli and Conia-ene type reactions in one pot.
Chemical communications (Cambridge, England), 2024, 60, 4234-4237
7132888 CIFC58 H46 O10I 1 2/a 17.6531; 20.7577; 37.5707
90; 92.335; 90
5963.6Zhang, Qiaoyu; Luo, Guiwen; Hu, Rui; Yang, Guoqiang; Chen, Jinping; Yu, Tianjun; Zeng, Yi; Li, Yi
Crystalline hydrogen-bonded organic framework for air-tolerant triplet-triplet annihilation upconversion.
Chemical communications (Cambridge, England), 2024, 60, 4475-4478
7132889 CIFC16 H21 N O2C 1 2/c 121.9697; 6.3504; 23.532
90; 114.886; 90
2978.3Liu, Ruzhang; Wang, Juan; Wu, Hao; Quan, Xianfeng; Wang, Shilin; Guo, Jiandong; Wang, Yang; Li, Heting
Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.
Chemical communications (Cambridge, England), 2024, 60, 4362-4365
7132890 CIFC24 H41 N O4P 21 21 216.372; 21.111; 17.2221
90; 90; 90
2316.7Liu, Ruzhang; Wang, Juan; Wu, Hao; Quan, Xianfeng; Wang, Shilin; Guo, Jiandong; Wang, Yang; Li, Heting
Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.
Chemical communications (Cambridge, England), 2024, 60, 4362-4365
7132891 CIFC32 H42 N2 O4P -15.6228; 11.5801; 22.772
88.886; 84.246; 83.434
1465.5Liu, Ruzhang; Wang, Juan; Wu, Hao; Quan, Xianfeng; Wang, Shilin; Guo, Jiandong; Wang, Yang; Li, Heting
Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.
Chemical communications (Cambridge, England), 2024, 60, 4362-4365
7132892 CIFC24 H39 N O3P 21 21 2110.4856; 14.332; 14.635
90; 90; 90
2199.3Liu, Ruzhang; Wang, Juan; Wu, Hao; Quan, Xianfeng; Wang, Shilin; Guo, Jiandong; Wang, Yang; Li, Heting
Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.
Chemical communications (Cambridge, England), 2024, 60, 4362-4365
7132893 CIFC35 H41 Cl4 O P RuP 1 21 110.0658; 15.252; 11.7038
90; 110.346; 90
1684.71Boym, Mikhail A.; Pototskiy, Roman A.; Podyacheva, Evgeniya S.; Chusov, Denis A.; Nelyubina, Yulia V.; Perekalin, Dmitry S.
Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C-H activation.
Chemical communications (Cambridge, England), 2024, 60, 4491-4494
7132894 CIFC15 H19 Br N2 O2P 1 21 17.049; 11.48; 19.45
90; 98.623; 90
1556.2Boym, Mikhail A.; Pototskiy, Roman A.; Podyacheva, Evgeniya S.; Chusov, Denis A.; Nelyubina, Yulia V.; Perekalin, Dmitry S.
Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C-H activation.
Chemical communications (Cambridge, England), 2024, 60, 4491-4494
7132895 CIFC28 H40 Cl4 Ru2P 1 21/c 112.2863; 18.7694; 12.3374
90; 93.047; 90
2841.06Boym, Mikhail A.; Pototskiy, Roman A.; Podyacheva, Evgeniya S.; Chusov, Denis A.; Nelyubina, Yulia V.; Perekalin, Dmitry S.
Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C-H activation.
Chemical communications (Cambridge, England), 2024, 60, 4491-4494
7132896 CIFC46 H55 Cl2 N2 O2 SbC 1 c 120.0826; 14.1346; 15.2463
90; 100.815; 90
4250.9Agou, Tomohiro; Kuroiwa, Shunsuke; Fukumoto, Hiroki; Nabeshima, Tatsuya
Synthesis and optical properties of antimony(V) complexes of a trianionic N<sub>2</sub>O<sub>2</sub>-type tetradentate dipyrrin ligand.
Chemical communications (Cambridge, England), 2024, 60, 4557-4560
7132897 CIFC49 H62 Cl N2 O4 SbP 1 21/c 124.3993; 16.832; 11.663
90; 100.297; 90
4712.7Agou, Tomohiro; Kuroiwa, Shunsuke; Fukumoto, Hiroki; Nabeshima, Tatsuya
Synthesis and optical properties of antimony(V) complexes of a trianionic N<sub>2</sub>O<sub>2</sub>-type tetradentate dipyrrin ligand.
Chemical communications (Cambridge, England), 2024, 60, 4557-4560
7132898 CIFC46 H57 N2 O4 SbP b c a28.4574; 27.9101; 32.3437
90; 90; 90
25688.9Agou, Tomohiro; Kuroiwa, Shunsuke; Fukumoto, Hiroki; Nabeshima, Tatsuya
Synthesis and optical properties of antimony(V) complexes of a trianionic N<sub>2</sub>O<sub>2</sub>-type tetradentate dipyrrin ligand.
Chemical communications (Cambridge, England), 2024, 60, 4557-4560
7132899 CIFC31 H37 N O3 S SiP -19.462; 9.6433; 17.6776
75.612; 75.789; 87.111
1514.5Zhang, Zhen; Lu, Lichao; Li, Guiling; Sheng, Xiaoyu; Zhang, Yijia; Yang, Lin; Zhao, Jiaqi; Xie, Lei; Li, Jiazhu; Sun, Kai
Radical cascade silylation/cyclization of 1,7-dienes to access silyl-substituted benzo[<i>b</i>]azepin-2-ones.
Chemical communications (Cambridge, England), 2024, 60, 4206-4209
7132900 CIFC17 H10 N2P 21 21 214.5044; 12.6636; 19.6473
90; 90; 90
1120.72Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132901 CIFC24 H14 N2 OP -17.6716; 9.16801; 12.73071
106.171; 91.1629; 109.967
801.64Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132902 CIFC25 H14 N2P 21 21 215.7818; 12.8402; 21.6872
90; 90; 90
1610.05Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132903 CIFC17 H12 N2 OC 1 2/c 116.3278; 7.4345; 21.1425
90; 99.071; 90
2534.37Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132904 CIFC23 H16 N2 OP 1 21/c 112.43235; 12.20419; 11.52302
90; 102.48; 90
1707.04Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132905 CIFC17 H9 N3 OP 1 21/c 13.77916; 16.2226; 19.1757
90; 93.565; 90
1173.35Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132906 CIFC23 H16 N2 OP -18.22512; 10.0169; 12.1195
104.088; 101.613; 109.165
870.66Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132907 CIFC19 H12 N2P 1 21/n 117.6032; 3.8528; 18.9019
90; 99.58; 90
1264.08Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132908 CIFC18 H21 N O6P 1 21/c 111.5445; 11.4051; 12.9631
90; 93.189; 90
1704.16Wen, Yongshun; Jin, Hong-Xian; Qiu, Yan-Hua; Zong, Yingtong; Luo, Wenjun; Chen, Zhengwang; Yu, Daohong
Photo-induced tungsten-catalyzed cascade synthesis of pyrrolo[2,1-<i>a</i>]isoquinoline-1,3-dicarboxylate and its reaction mechanism.
Chemical communications (Cambridge, England), 2024, 60, 4573-4576
7132909 CIFC44 H44 O10P -115.186; 15.823; 16.474
69.815; 88.884; 81.886
3676.4Soliman, Luc; Ramassamy, Elsa; Dujarric, Katia; Naulet, Guillaume; Dechambenoit, Pierre; Bock, Harald; Durola, Fabien
Coronenes with push-pull geometries from macrocycle-forming Perkin condensations.
Chemical communications (Cambridge, England), 2024, 60, 4439-4442
7132910 CIFC36 H28 O8P -16.9314; 13.781; 16.068
86.662; 82.997; 76.021
1477.62Soliman, Luc; Ramassamy, Elsa; Dujarric, Katia; Naulet, Guillaume; Dechambenoit, Pierre; Bock, Harald; Durola, Fabien
Coronenes with push-pull geometries from macrocycle-forming Perkin condensations.
Chemical communications (Cambridge, England), 2024, 60, 4439-4442
7132911 CIFC38 H38 B Cl4 F6 N S SbP c c n8.895; 16.5456; 27.257
90; 90; 90
4011.5Cosby, Taylor P. L.; Bhattacharjee, Avik; Henneberry, Samantha K.; LeBlanc, Jesse; Caputo, Christopher B.
Unlocking Lewis acidity <i>via</i> the redox non-innocence of a phenothiazine-substituted borane.
Chemical communications (Cambridge, England), 2024, 60, 5391-5394
7132912 CIFC20 H14 N2 O6 WC 1 2/c 116.6532; 10.7273; 11.4809
90; 103.498; 90
1994.3Song, Heng; Xiao, Yuting; Wei, Jingjing; Liu, Yuzan; Yang, Liqing; Bai, Pengtao; Yang, Fu; Yu, Kai; Xu, Chen; Cai, Xingwei
Low-valent-tungsten catalysis enables hydroboration of esters and nitriles.
Chemical communications (Cambridge, England), 2024, 60, 5026-5029
7132913 CIFC10 H14 Br4 F N2 ZnP 1 21/c 18.0955; 20.9526; 9.8012
90; 102.25; 90
1624.64Wang, Yu-Yin; Kang, Huai-Yuan; Zhang, Shao-Ya; Qu, Hao; Zhu, Lin; Zhao, Dan; Li, Xian-Feng; Lei, Xiao-Wu; Yue, Cheng-Yang
Exploring 0D lead-free metal halide with highly efficient blue light emission and high-sensitivity photodetection.
Chemical communications (Cambridge, England), 2024, 60, 2784-2787
7132914 CIFC21 H28 Cl2 Co N3P 1 21/n 110.4791; 15.9525; 12.9626
90; 99.6049; 90
2136.55Boity, Biswaranjan; Sidiqque, Misba; Rit, Arnab
Amine-functionalized bifunctional Co<sup>III</sup>-NHC complexes: highly effective phosphine-free catalysts for the α-alkylation of nitriles.
Chemical communications (Cambridge, England), 2024, 60, 3142-3145
7132915 CIFC8 H5.5 N1.5 O0.5P 21 21 213.741; 17.187; 18.371
90; 90; 90
1181.19Sarkar, Souradip; Bhunya, Sourav; Pan, Subarna; Datta, Arnadeep; Roy, Lisa; Samanta, Rajarshi
Rh(II)-catalysed <i>N</i><sup>2</sup>-selective arylation of benzotriazoles and indazoles using quinoid carbenes <i>via</i> 1,5-H shift.
Chemical communications (Cambridge, England), 2024, 60, 4727-4730
7132916 CIFC17 H12 N2 OP b c a11.511; 10.247; 21.356
90; 90; 90
2519Sarkar, Souradip; Bhunya, Sourav; Pan, Subarna; Datta, Arnadeep; Roy, Lisa; Samanta, Rajarshi
Rh(II)-catalysed <i>N</i><sup>2</sup>-selective arylation of benzotriazoles and indazoles using quinoid carbenes <i>via</i> 1,5-H shift.
Chemical communications (Cambridge, England), 2024, 60, 4727-4730
7132917 CIFC31 H29 N O5P -110.8447; 11.198; 12.0881
101.529; 90.637; 113.153
1315.93Pramanik, Sourav; Hazra, Subhadeep; Chatterjee, Ayan; Saha, Jaideep
Hydrogen bonding-promoted tunable approach for access to aza-bicyclo-[3.3.0]octanes and cyclopenta[<i>b</i>] pyrroles.
Chemical communications (Cambridge, England), 2024, 60, 4922-4925
7132918 CIFC56 H40 As4 Cl4 Cu4 Mo8 O16 Sb4P -115.055; 15.1827; 17.1422
89.358; 89.116; 69.16
3661.4Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132919 CIFC15 H12 As Cl2 Cu I Mo2 O4 SbP 1 21/n 110.4347; 15.6404; 13.4725
90; 92.374; 90
2196.86Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132920 CIFC56 H40 As4 Br4 Cu4 Mo8 O16 Sb4P -114.9733; 15.0851; 17.339
89.022; 88.933; 70.588
3692.9Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132921 CIFC67 H25 Al As2 Cl2 Cu F46 Mo4 N O11 Sb2P 1 21/c 120.9582; 33.303; 12.1289
90; 105.237; 90
8168.03Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132922 CIFC129 H42 Ag2 Al2 As4 Cl2 F92 Mo8 O22 Sb4P 1 21/n 111.4664; 40.5323; 33.5837
90; 91.704; 90
15601.4Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132923 CIFC108.8 H34.6 Al2 As2 Cl5.6 Cu2 F92 Mo4 N3 O14 Sb2P 1 21/n 123.6343; 19.0078; 31.4538
90; 98.5123; 90
13974.5Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132924 CIFC30 H30 Si3P 1 21/c 19.9325; 18.2411; 15.0008
90; 102.356; 90
2654.89Wakefield, 4th, Herbert; Melvin, Sophia J.; Jiang, Jennifer; Kevlishvili, Ilia; Siegler, Maxime A.; Craig, Stephen L.; Kulik, Heather J.; Klausen, Rebekka S.
Angle-strained sila-cycloalkynes.
Chemical communications (Cambridge, England), 2024, 60, 4842-4845
7132925 CIFC37 H37 N3 Si3P 1 21/c 112.98096; 26.6317; 10.50266
90; 91.5598; 90
3629.48Wakefield, 4th, Herbert; Melvin, Sophia J.; Jiang, Jennifer; Kevlishvili, Ilia; Siegler, Maxime A.; Craig, Stephen L.; Kulik, Heather J.; Klausen, Rebekka S.
Angle-strained sila-cycloalkynes.
Chemical communications (Cambridge, England), 2024, 60, 4842-4845
7132926 CIFC32 H36 Si4P 1 21/c 124.3501; 11.0409; 25.4353
90; 115.708; 90
6161.3Wakefield, 4th, Herbert; Melvin, Sophia J.; Jiang, Jennifer; Kevlishvili, Ilia; Siegler, Maxime A.; Craig, Stephen L.; Kulik, Heather J.; Klausen, Rebekka S.
Angle-strained sila-cycloalkynes.
Chemical communications (Cambridge, England), 2024, 60, 4842-4845
7132927 CIFC35 H25 N O2 SP -18.8511; 10.7751; 14.2389
81.33; 88.876; 74.316
1292.16Malik, Nirmal; De, Ritobrata; Pal, Santanu Kumar; Ramasastry, S. S. V.
A one-pot telescopic synthesis of benzo[<i>b</i>]carbazoles and exploration of their liquid crystalline properties.
Chemical communications (Cambridge, England), 2024, 60, 4797-4800
7132928 CIFC90 H80 B2 N6 Ni2 O4C 1 2/c 132.431; 24.9205; 24.931
90; 123.299; 90
16841Patra, Suman; Atta, Sayan; Ghosh, Soumili; Majumdar, Amit; Dey, Abhishek
Kinetic isotope effect offers selectivity in CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 4826-4829
7132929 CIFC19 H22 Cl N3 Ni O7P 1 21/c 19.1074; 16.575; 14.4535
90; 107.064; 90
2085.8Patra, Suman; Atta, Sayan; Ghosh, Soumili; Majumdar, Amit; Dey, Abhishek
Kinetic isotope effect offers selectivity in CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 4826-4829
7132930 CIFC62 H66 N6 O17 P4 U2C 1 2/c 131.0258; 12.8733; 16.8307
90; 114.157; 90
6133.6Yang, Xiaofan; Fang, Dong; Wang, Shihui; Tian, Zhenjiang; Xu, Lei; Liu, Jiyong; Zhang, Anyun; Xiao, Chengliang
Epimerization effects on coordination behaviours of phenanthroline-based phosphine-oxide ligands with uranyl ions.
Chemical communications (Cambridge, England), 2024, 60, 5042-5045
7132931 CIFC28 H26 N2 O2 P2P 1 21/c 110.1143; 28.2649; 8.4249
90; 98.202; 90
2383.87Yang, Xiaofan; Fang, Dong; Wang, Shihui; Tian, Zhenjiang; Xu, Lei; Liu, Jiyong; Zhang, Anyun; Xiao, Chengliang
Epimerization effects on coordination behaviours of phenanthroline-based phosphine-oxide ligands with uranyl ions.
Chemical communications (Cambridge, England), 2024, 60, 5042-5045
7132932 CIFC56 H52 N10 O28 P4 U3P 1 21/c 119.1125; 10.6852; 17.9947
90; 107.716; 90
3500.6Yang, Xiaofan; Fang, Dong; Wang, Shihui; Tian, Zhenjiang; Xu, Lei; Liu, Jiyong; Zhang, Anyun; Xiao, Chengliang
Epimerization effects on coordination behaviours of phenanthroline-based phosphine-oxide ligands with uranyl ions.
Chemical communications (Cambridge, England), 2024, 60, 5042-5045
7132933 CIFC28 H26 N2 O2 P2P -18.231; 11.7984; 13.6524
73.829; 85.363; 76.865
1239.83Yang, Xiaofan; Fang, Dong; Wang, Shihui; Tian, Zhenjiang; Xu, Lei; Liu, Jiyong; Zhang, Anyun; Xiao, Chengliang
Epimerization effects on coordination behaviours of phenanthroline-based phosphine-oxide ligands with uranyl ions.
Chemical communications (Cambridge, England), 2024, 60, 5042-5045
7132934 CIFC72 H98 S2 TmP -113.2573; 14.2636; 18.3627
104.34; 93.693; 98.57
3307.9Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132935 CIFC72 H98 I Nd S2P -113.3492; 14.1047; 18.6556
102.433; 94.721; 99.287
3360.2Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132936 CIFC72 H98 Nd S2P -113.2169; 14.2162; 18.5245
104.917; 93.8221; 97.9184
3312.3Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132937 CIFC72 H98 I La S2P -113.2786; 14.2335; 18.678
102.71; 94.255; 99.004
3379.5Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132938 CIFC72 H98 I0.13 La S2P -113.209; 14.2623; 18.5499
104.544; 93.628; 98.433
3327.73Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132939 CIFC84 H108 N2 S2 SmP b c n16.0032; 18.7417; 24.3011
90; 90; 90
7288.6Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132940 CIFC84 H108 N2 Nd S2P b c n15.9566; 18.7918; 24.254
90; 90; 90
7272.6Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132941 CIFC17 H22 N2 O2 SP 1 21 110.9048; 14.2184; 11.9956
90; 110.377; 90
1743.51Wei, Tao; Xie, Ming-Sheng; Guo, Hai-Ming
Construction of thioglycoside bonds <i>via</i> an asymmetric organocatalyzed sulfa-Michael/aldol reaction: access to 4'-thionucleosides.
Chemical communications (Cambridge, England), 2024, 60, 5018-5021
7132942 CIFC23 H18 N2 O SP 1 21/n 18.252; 14.7387; 15.4992
90; 96.548; 90
1872.8Wang, Xinxin; Wang, Jie; Ji, Meishan; Wu, Xinxin; Zhu, Chen
<i>Z</i>-selective radical difunctionalization of aromatic alkynes: synthesis of multi-substituted triarylethenes.
Chemical communications (Cambridge, England), 2024, 60, 4894-4897
7132943 CIFC23 H16 F N O SC 1 2/c 112.5347; 15.7748; 19.3093
90; 98.0108; 90
3780.8Wang, Xinxin; Wang, Jie; Ji, Meishan; Wu, Xinxin; Zhu, Chen
<i>Z</i>-selective radical difunctionalization of aromatic alkynes: synthesis of multi-substituted triarylethenes.
Chemical communications (Cambridge, England), 2024, 60, 4894-4897
7132944 CIFC100 H86 N2 O32 P4 W10P -113.5793; 15.3135; 15.4699
117.216; 113.848; 92.658
2508.49Gu, Chen; Yatabe, Takafumi; Yamaguchi, Kazuya; Suzuki, Kosuke
Photocatalytic aerobic α-oxygenation of amides to imides using a highly durable decatungstate tetraphenylphosphonium salt.
Chemical communications (Cambridge, England), 2024, 60, 4906-4909
7132945 CIFC41.5 H21.5 Cl0.25 N5 O5.5P 1 21/m 112.7611; 18.5038; 14.1018
90; 100.643; 90
3272.56Zhang, Fan; Du, Xu-Sheng; Song, Kui-Zhu; Han, Ying; Lu, Hai-Yan; Chen, Chuan-Feng
A calix[3]carbazole-based cavitand: synthesis, structure and its complexation with fullerenes.
Chemical communications (Cambridge, England), 2024, 60, 4962-4965
7132946 CIFC81.46 H39.92 Cl0.92 N9 O6I 1 2/a 130.8326; 13.5754; 31.1005
90; 106.96; 90
12451.4Zhang, Fan; Du, Xu-Sheng; Song, Kui-Zhu; Han, Ying; Lu, Hai-Yan; Chen, Chuan-Feng
A calix[3]carbazole-based cavitand: synthesis, structure and its complexation with fullerenes.
Chemical communications (Cambridge, England), 2024, 60, 4962-4965
7132947 CIFC153 H47 Cl4 N9 O6P 1 21/n 113.0791; 32.0488; 27.0224
90; 94.916; 90
11285.3Zhang, Fan; Du, Xu-Sheng; Song, Kui-Zhu; Han, Ying; Lu, Hai-Yan; Chen, Chuan-Feng
A calix[3]carbazole-based cavitand: synthesis, structure and its complexation with fullerenes.
Chemical communications (Cambridge, England), 2024, 60, 4962-4965
7132948 CIFC163 H47 Cl4 N9 O6P 1 21/n 126.5926; 32.943; 30.1206
90; 113.007; 90
24288Zhang, Fan; Du, Xu-Sheng; Song, Kui-Zhu; Han, Ying; Lu, Hai-Yan; Chen, Chuan-Feng
A calix[3]carbazole-based cavitand: synthesis, structure and its complexation with fullerenes.
Chemical communications (Cambridge, England), 2024, 60, 4962-4965
7132949 CIFC20 H6 Cl8 NP 1 21/c 114.0305; 8.0731; 18.9296
90; 94.608; 90
2137.2Lv, Kuo; Zhang, Minzhe; Xia, Xin; Liu, Wenjing; Wan, Keke; Zhang, Ming; Li, Feng
Cyano modified triphenylmethyl radical skeletons: higher stability and efficiency.
Chemical communications (Cambridge, England), 2024, 60, 4846-4849
7132950 CIFC21 H6 Cl7 N2P -18.2197; 11.2036; 13.6336
67.189; 84.761; 73.004
1106.4Lv, Kuo; Zhang, Minzhe; Xia, Xin; Liu, Wenjing; Wan, Keke; Zhang, Ming; Li, Feng
Cyano modified triphenylmethyl radical skeletons: higher stability and efficiency.
Chemical communications (Cambridge, England), 2024, 60, 4846-4849
7132951 CIFC26 H22 Cl N O2P -17.7575; 11.8553; 12.4714
68.379; 88.015; 75.886
1032.14Sui, Jia-Li; Zhong, Long-Jin; Xiong, Bi-Quan; Tang, Ke-Wen; Liu, Yu
Regioselective synthesis of N-containing polycyclic compounds <i>via</i> radical annulation cyclization of 1,7-dienes with aldehydes.
Chemical communications (Cambridge, England), 2024, 60, 4834-4837
7132952 CIFC16 H19 N O2P 1 21/c 116.3685; 10.1416; 33.0222
90; 92.147; 90
5477.93Liu, Zhaosheng; Ji, Xiaochen; Duan, Lilan; Deng, Guo-Jun; Huang, Huawen
Accessing pyrrolo[1,2-<i>a</i>]indole derivatives <i>via</i> visible-light-induced dearomatizative cyclization of indoles.
Chemical communications (Cambridge, England), 2024, 60, 4902-4905
7132953 CIFC13 H15 N O2P 1 21/c 119.4445; 8.085; 15.4094
90; 111.936; 90
2247.1Liu, Zhaosheng; Ji, Xiaochen; Duan, Lilan; Deng, Guo-Jun; Huang, Huawen
Accessing pyrrolo[1,2-<i>a</i>]indole derivatives <i>via</i> visible-light-induced dearomatizative cyclization of indoles.
Chemical communications (Cambridge, England), 2024, 60, 4902-4905
7132954 CIFC40 H36 N2 O2P -112.0197; 12.0255; 13.0084
87.125; 64.484; 67.794
1556.7Ishikawa, Shuhei; Sakamaki, Daisuke; Gon, Masayuki; Tanaka, Kazuo; Fujiwara, Hideki
Solvent-free synthesis and chiroptical properties of a C-N axially chiral cruciform dimer of benzo[<i>b</i>]phenoxazine.
Chemical communications (Cambridge, England), 2024, 60, 4946-4949
7132955 CIFC172 H172 N8 O8P 112.3589; 12.8347; 22.1604
79.4229; 87.2486; 87.6565
3449.59Ishikawa, Shuhei; Sakamaki, Daisuke; Gon, Masayuki; Tanaka, Kazuo; Fujiwara, Hideki
Solvent-free synthesis and chiroptical properties of a C-N axially chiral cruciform dimer of benzo[<i>b</i>]phenoxazine.
Chemical communications (Cambridge, England), 2024, 60, 4946-4949
7132956 CIFC86 H86 N4 O4P 112.3589; 12.8455; 22.1587
79.4344; 87.2227; 87.6319
3452.24Ishikawa, Shuhei; Sakamaki, Daisuke; Gon, Masayuki; Tanaka, Kazuo; Fujiwara, Hideki
Solvent-free synthesis and chiroptical properties of a C-N axially chiral cruciform dimer of benzo[<i>b</i>]phenoxazine.
Chemical communications (Cambridge, England), 2024, 60, 4946-4949
7132957 CIFC18 H17 N O2P 1 21/c 16.3783; 7.1006; 31.5404
90; 93.88; 90
1425.18Gao, Ying; Wang, Mingxu; Sun, Jingxian; Zhao, Xiao-Jing; He, Yonghui
Electrochemical-induced solvent-tuned selective C(sp<sup>3</sup>)-H bond activation towards the synthesis of C3-functionalized chromone derivatives.
Chemical communications (Cambridge, England), 2024, 60, 5050-5053
7132958 CIFC50 H45 B2 F4 N5 O2P -112.912; 16.473; 22.588
71.34; 83.507; 79.792
4471.7Wang, Long; Cheng, Cheng; Yu, Changjiang; Wu, Qinghua; Kang, Zhengxin; Wang, Hua; Jiao, Lijuan; Hao, Erhong
NIR-absorbing and emitting α,α-nitrogen-bridged BODIPY dimers with strong excitonic coupling.
Chemical communications (Cambridge, England), 2024, 60, 5054-5057
7132959 CIFC17 H14 F N OP n a 2112.4495; 20.4914; 5.0901
90; 90; 90
1298.52Liu, Hongxin; Tang, Tingyu; Li, Bin; Wang, Baiquan
Manganese(I)-catalyzed nucleophilic addition of C(sp<sup>3</sup>)-H bonds to aldehydes.
Chemical communications (Cambridge, England), 2024, 60, 5066-5069
7132960 CIFC14 H8 Mn N O4P 1 21/n 17.631; 8.00772; 20.9823
90; 98.411; 90
1268.37Liu, Hongxin; Tang, Tingyu; Li, Bin; Wang, Baiquan
Manganese(I)-catalyzed nucleophilic addition of C(sp<sup>3</sup>)-H bonds to aldehydes.
Chemical communications (Cambridge, England), 2024, 60, 5066-5069
7132961 CIFC34 H34 S2R -3 :H37.256; 37.256; 5.1212
90; 90; 120
6155.9Su, Yangzhe; Wang, Min; Xu, Jianping; Chen, Weinan; Zhou, Gang
C-H arylation of thiopyran derivatives with aryl halides.
Chemical communications (Cambridge, England), 2024, 60, 5193-5196
7132962 CIFC30 H22 SP 1 21/c 114.9168; 5.1215; 80.8465
90; 92.323; 90
6171.3Su, Yangzhe; Wang, Min; Xu, Jianping; Chen, Weinan; Zhou, Gang
C-H arylation of thiopyran derivatives with aryl halides.
Chemical communications (Cambridge, England), 2024, 60, 5193-5196
7132963 CIFC27 H24 SP -112.0192; 13.1986; 13.5978
91.326; 92.661; 113.371
1975.96Su, Yangzhe; Wang, Min; Xu, Jianping; Chen, Weinan; Zhou, Gang
C-H arylation of thiopyran derivatives with aryl halides.
Chemical communications (Cambridge, England), 2024, 60, 5193-5196
7132964 CIFC19 H19 F3 N2P 1 21/c 110.34; 15.24; 11.008
90; 94.938; 90
1728.2Yang, Ming; Meng, Yu-Xuan; Mehfooz, Haroon; Zhao, Yu-Long
Visible light-promoted [3+2] cyclization reaction of vinyl azides with perfluoroalkyl-substituted-imidoyl sulfoxonium ylides.
Chemical communications (Cambridge, England), 2024, 60, 5407-5410
7132965 CIFC34 H33 N O2P 1 21/c 121.901; 11.9356; 10.1958
90; 95.864; 90
2651.3Pramanik, Shyamal; Samanta, Apurba; Maity, Soumitra
A two carbon homologation of Friedel-Crafts alkylation enabled by photochemical alkene stitching: modular assembly of cyclolignans.
Chemical communications (Cambridge, England), 2024, 60, 5282-5285
7132966 CIFC22 H26 O6P 1 21/c 113.0879; 11.0775; 14.0938
90; 102.597; 90
1994.1Pramanik, Shyamal; Samanta, Apurba; Maity, Soumitra
A two carbon homologation of Friedel-Crafts alkylation enabled by photochemical alkene stitching: modular assembly of cyclolignans.
Chemical communications (Cambridge, England), 2024, 60, 5282-5285
7132967 CIFC18 H16 N12 O8 S Zn3P 1 21/c 114.143; 9.9829; 25.111
90; 96.777; 90
3520.6Deng, Yu-Xin; Yang, Guo-Ping; Wang, Yao-Yu
Pure separation of acetylene based on a sulfonic acid and amino group functionalized Zn-MOF.
Chemical communications (Cambridge, England), 2024, 60, 5046-5049
7132968 CIFC18 H14 N12 O7 S Zn3P 1 21/c 114.0795; 9.851; 25.9541
90; 95.909; 90
3580.6Deng, Yu-Xin; Yang, Guo-Ping; Wang, Yao-Yu
Pure separation of acetylene based on a sulfonic acid and amino group functionalized Zn-MOF.
Chemical communications (Cambridge, England), 2024, 60, 5046-5049
7132969 CIFC32 H28 Cl2 O8P -19.951; 10.5842; 14.9945
96.395; 99.389; 117.914
1344.5Kelsey, Shaun R.; Griaznov, Georgii; Spaeth, Andrew D.; Janzen, Daron E.; Douglas, Justin T.; Thompson, Ward H.; Barybin, Mikhail V.
Tuning the redox profile of the 6,6'-biazulenic platform through functionalization along its molecular axis.
Chemical communications (Cambridge, England), 2024, 60, 5213-5216
7132970 CIFFe Nb Te2P 1 21/c 17.28; 6.305; 7.992
90; 92.33; 90
366.5Stepanova, Anna V.; Mironov, Andrei V.; Bogach, Alexey V.; Azarevich, Andrey N.; Presniakov, Igor A.; Sobolev, Alexey V.; Pankratov, Denis A.; Zayakhanov, Vladimir A.; Starchikov, Sergey S.; Verchenko, Valeriy Yu; Shevelkov, Andrei V.
Bulk ferromagnetism in cleavable van der Waals telluride NbFeTe<sub>2</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5518-5521
7132971 CIFC52 H46 F3 Fe N3 P2P -111.711; 12.5996; 16.8271
96.344; 100.608; 116.094
2139.53Stevens, Jeremiah E.; Miller, Justin D.; Fitzsimmons, Matthew C.; Moore, Curtis E.; Thomas, Christine M.
<i>Z</i>-selective dimerization of terminal alkynes by a (PNNP)Fe<sup>II</sup> complex.
Chemical communications (Cambridge, England), 2024, 60, 5169-5172
7132972 CIFC48 H50 Fe N4 P2P -110.7765; 13.6127; 14.6156
90.015; 96.865; 100.703
2091.1Stevens, Jeremiah E.; Miller, Justin D.; Fitzsimmons, Matthew C.; Moore, Curtis E.; Thomas, Christine M.
<i>Z</i>-selective dimerization of terminal alkynes by a (PNNP)Fe<sup>II</sup> complex.
Chemical communications (Cambridge, England), 2024, 60, 5169-5172
7132973 CIFC60 H52 F6 Fe N2 O P2P -113.4659; 13.8415; 14.7796
93.409; 105.088; 106.332
2526.2Stevens, Jeremiah E.; Miller, Justin D.; Fitzsimmons, Matthew C.; Moore, Curtis E.; Thomas, Christine M.
<i>Z</i>-selective dimerization of terminal alkynes by a (PNNP)Fe<sup>II</sup> complex.
Chemical communications (Cambridge, England), 2024, 60, 5169-5172
7132974 CIFC78 H64 F4 Fe N2 P2C 1 2/c 129.4666; 13.8824; 16.5411
90; 114.212; 90
6171.2Stevens, Jeremiah E.; Miller, Justin D.; Fitzsimmons, Matthew C.; Moore, Curtis E.; Thomas, Christine M.
<i>Z</i>-selective dimerization of terminal alkynes by a (PNNP)Fe<sup>II</sup> complex.
Chemical communications (Cambridge, England), 2024, 60, 5169-5172
7132975 CIFC26 H20 N2 O3I 1 2/a 115.6096; 16.4461; 16.1674
90; 96.743; 90
4121.74Zhao, Shuang; Chen, Mengxiao; Zhou, Wenlu; Ni, Dan; Li, Zhenghua; Nie, Shenyou; He, Yi
Green synthesis for diverse bioactive benzo-fused spiroindolines through DBU-catalysed post-Ugi double cyclization.
Chemical communications (Cambridge, England), 2024, 60, 5455-5458
7132976 CIFC28 H18 N2 O4P -110.0719; 10.5354; 10.8948
92.2576; 111.172; 93.0417
1074.38Akbari, Alireza; Khosravi, Hormoz; Bauer, Felix; Rominger, Frank; Breit, Bernhard; Balalaie, Saeed
Metal- and solvent-free domino reaction of 2-isocyanophenol esters to benzoxazines: long-range 1,5-acyl migration on 1,4-diazabutatriene.
Chemical communications (Cambridge, England), 2024, 60, 5451-5454
7132977 CIFC16 H13 N O3P -16.7066; 8.7863; 12.6844
100.298; 96.3058; 111.389
672.14Akbari, Alireza; Khosravi, Hormoz; Bauer, Felix; Rominger, Frank; Breit, Bernhard; Balalaie, Saeed
Metal- and solvent-free domino reaction of 2-isocyanophenol esters to benzoxazines: long-range 1,5-acyl migration on 1,4-diazabutatriene.
Chemical communications (Cambridge, England), 2024, 60, 5451-5454
7132978 CIFC97 H203 Ag45 Nb6 O47 S23P b c a28.7435; 28.3372; 48.7703
90; 90; 90
39723.9Zhao, Zichen; Zhao, Mengyun; Deng, Lan; Li, Qing; Zhang, Jing; Su, Haifeng; Lv, Hongjin; Yang, Guo-Yu
Two structurally new Lindqvist hexaniobate-templated silver thiolate clusters.
Chemical communications (Cambridge, England), 2024, 60, 5415-5418
7132979 CIFC82 H210 Ag41 K Nb6 O42.5 S26.5P 42 21 232.1512; 32.1512; 17.6732
90; 90; 90
18268.8Zhao, Zichen; Zhao, Mengyun; Deng, Lan; Li, Qing; Zhang, Jing; Su, Haifeng; Lv, Hongjin; Yang, Guo-Yu
Two structurally new Lindqvist hexaniobate-templated silver thiolate clusters.
Chemical communications (Cambridge, England), 2024, 60, 5415-5418
7132980 CIFC32 H72 Cu2 I4 P2P -112.4248; 12.9746; 16.828
86.253; 75.221; 64.491
2364.3Delafoulhouze, Jérémy; Cordier, Marie; Mevellec, Jean-Yves; Massuyeau, Florian; Hernandez, Olivier; Latouche, Camille; Perruchas, Sandrine
Mechanoresponsive luminescence triggered by phase transition of a supercooled copper(I) complex.
Chemical communications (Cambridge, England), 2024, 60, 5278-5281
7132981 CIFC8 H3 O5 TiI 41 2 215.1203; 15.1203; 11.9863
90; 90; 90
2740.35Zeng, Xiangdi; Li, Jiangnan; He, Meng; Lu, Wanpeng; Crawshaw, Danielle; Guo, Lixia; Ma, Yujie; Kippax-Jones, Meredydd; Cheng, Yongqiang; Manuel, Pascal; Rudić, Svemir; Frogley, Mark D.; Schröder, Martin; Yang, Sihai
High adsorption of ammonia in a titanium-based metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 5912-5915
7132982 CIFC8 H3 D1.25 N0.42 O5 TiI 41 2 215.0507; 15.0507; 12.0595
90; 90; 90
2731.8Zeng, Xiangdi; Li, Jiangnan; He, Meng; Lu, Wanpeng; Crawshaw, Danielle; Guo, Lixia; Ma, Yujie; Kippax-Jones, Meredydd; Cheng, Yongqiang; Manuel, Pascal; Rudić, Svemir; Frogley, Mark D.; Schröder, Martin; Yang, Sihai
High adsorption of ammonia in a titanium-based metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 5912-5915
7132983 CIFC8 H3 D3.82 N1.27 O5 TiI 41 2 214.92; 14.92; 12.1536
90; 90; 90
2705.47Zeng, Xiangdi; Li, Jiangnan; He, Meng; Lu, Wanpeng; Crawshaw, Danielle; Guo, Lixia; Ma, Yujie; Kippax-Jones, Meredydd; Cheng, Yongqiang; Manuel, Pascal; Rudić, Svemir; Frogley, Mark D.; Schröder, Martin; Yang, Sihai
High adsorption of ammonia in a titanium-based metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 5912-5915
7132984 CIFC36 H32 N2 O11 Pb2P 1 21/n 116.46; 11.3441; 19.5207
90; 94.325; 90
3634.6Luo, Qi; Li, Yuxia; Huang, Xin; Zheng, Yi; Gu, Qi; Wang, Shuaihua; Wu, Shaofan
Tetraphenylene-based semiconductive metal-organic framework crystals for direct X-ray detection and imaging.
Chemical communications (Cambridge, England), 2024, 60, 5510-5513
7132985 CIFC19 H15 Cl2 N O3P 1 21/c 116.1234; 11.9822; 8.9939
90; 94.945; 90
1731.1Harsha, ?; Kumar, Rohit; Jain, Nidhi
<sup>1</sup>O<sub>2</sub> mediated synthesis of carbonyl substituted quinoline-2,4(1<i>H</i>,3<i>H</i>)-diones in visible light: 4CzIPN as a reusable photocatalyst.
Chemical communications (Cambridge, England), 2024, 60, 5646-5649
7132986 CIFC148 H188 F12 Fe2 N18 O28 S4P 1 21/m 116.4651; 23.3184; 17.2067
90; 97.467; 90
6550.3Mobili, Riccardo; Preda, Giovanni; Dondi, Daniele; Monzani, Enrico; Vadivel, Dhanalakshmi; Massera, Chiara; Pasini, Dario; Amendola, Valeria
Triptycene-based diiron(II) mesocates: spin-crossover in solution.
Chemical communications (Cambridge, England), 2024, 60, 5522-5525
7132987 CIFC246 H340 F12 N34 O33 P2P -121.5297; 24.7451; 29.6954
109.868; 104.145; 101.331
13733.1Huang, Song; Wang, Zhenwen; Wu, Jinyang; Mai, Xinyan; Qin, Song; Zhou, Yuqiao; Yuan, Daqiang; Li, Xiaowei; Feng, Wen; Yuan, Lihua
A molecular sheaf: doubly threaded [6]rotaxane.
Chemical communications (Cambridge, England), 2024, 60, 5622-5625
7132988 CIFC16 H24 Au B3 F12 N8C 1 2/c 115.3073; 15.711; 22.0225
90; 99.885; 90
5217.63Barwise, Lachlan; Moon, Lachlan J.; Dhakal, Bibidh; Hogan, Conor F.; White, Keith F.; Dutton, Jason L.
An extremely electron poor Au(III) trication bearing acetonitrile ligands.
Chemical communications (Cambridge, England), 2024, 60, 5586-5589
7132989 CIFC21 H29 Au B2 F8 N6P 1 21 19.4083; 19.422; 15.7483
90; 103.473; 90
2798.46Barwise, Lachlan; Moon, Lachlan J.; Dhakal, Bibidh; Hogan, Conor F.; White, Keith F.; Dutton, Jason L.
An extremely electron poor Au(III) trication bearing acetonitrile ligands.
Chemical communications (Cambridge, England), 2024, 60, 5586-5589
7132990 CIFC198 H251 N6 O46P 1 21/n 122.4005; 26.9673; 32.2242
90; 90.916; 90
19463.5Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132991 CIFC152.46 H189.38 N6 O23.23 S13.23P -121.1953; 26.1285; 31.3285
73.564; 72.242; 68.045
15042Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132992 CIFC190 H208 N6 O58C 1 2/c 139.4383; 27.5839; 35.2015
90; 109.998; 90
35985.4Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132993 CIFC174 H256 N6 O34 S24P 63 2 219.9064; 19.9064; 33.451
90; 90; 120
11479.6Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132994 CIFC138 H148 N6 O16 S6P -121.6989; 27.1612; 27.6258
94.1928; 111.564; 109.903
13867Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132995 CIFC342 H393 N12 O80.01P -121.4803; 27.0745; 29.3858
94.133; 108.263; 112.968
14568.6Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132996 CIFC154.5 H176.5 N15.5 O19.5P -121.6013; 27.1502; 28.3933
93.864; 111.256; 110.441
14178.7Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132997 CIFC132 H130 N6 O13 S3I 1 2 151.7627; 21.7575; 57.0058
90; 90.443; 90
64199.5Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132998 CIFC17 H10 F5 N3P 1 21/c 114.4065; 6.1767; 17.7705
90; 109.917; 90
1486.72Das, Animesh; Maji, Biplab
Substrate-controlled divergent remote C-H and N-H polyfluoroarylation of 2-aminopyrimidines with polyfluoroarenes <i>via</i> Pd(II)/Pd(0) catalysis.
Chemical communications (Cambridge, England), 2024, 60, 5630-5633
7132999 CIFC15 H14 F5 N3P 1 21/c 112.4951; 7.6806; 16.1712
90; 108.511; 90
1471.65Das, Animesh; Maji, Biplab
Substrate-controlled divergent remote C-H and N-H polyfluoroarylation of 2-aminopyrimidines with polyfluoroarenes <i>via</i> Pd(II)/Pd(0) catalysis.
Chemical communications (Cambridge, England), 2024, 60, 5630-5633
7133000 CIFC20 H20 Cl4 N4 NpC 1 2/c 119.2449; 9.5303; 15.6081
90; 127.522; 90
2270.4Lopez, Lauren M.; Uible, Madeleine C.; Zeller, Matthias; Bart, Suzanne C.
Lewis base adducts of NpCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5956-5959
7133001 CIFC8 H12 Cl4 N4 NpC 1 2/c 114.6308; 8.4327; 13.7095
90; 91.687; 90
1690.71Lopez, Lauren M.; Uible, Madeleine C.; Zeller, Matthias; Bart, Suzanne C.
Lewis base adducts of NpCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5956-5959
7133002 CIFC36 H30 Cl4 Np O2 P2P 1 21 19.9552; 15.3552; 11.9194
90; 98.955; 90
1799.84Lopez, Lauren M.; Uible, Madeleine C.; Zeller, Matthias; Bart, Suzanne C.
Lewis base adducts of NpCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5956-5959
7133003 CIFC45.76 H67.53 Cl4 N4 Np O2.44P 1 21/n 116.6555; 11.535; 25.751
90; 94.5345; 90
4931.8Lopez, Lauren M.; Uible, Madeleine C.; Zeller, Matthias; Bart, Suzanne C.
Lewis base adducts of NpCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5956-5959
7133004 CIFC18 H20 O3C 1 2/c 133.38; 5.972; 18.656
90; 119.978; 90
3221Kumar, Rakesh; Dutt, Shiv; Banerjee, Prabal
Electrochemical oxidative C-C bond cleavage of methylenecyclopropanes with alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4246-4249
7133005 CIFC23 H22 N2 OP c a 2110.0123; 18.3467; 10.107
90; 90; 90
1856.58Kumar, Dharmendra; Unnikrishnan, Urmila; Kuram, Malleswara Rao
Facile access to <i>C</i>-substituted piperazin-2-ones and mianserin derivative enabled by chemoselective carbene insertion and cyclization cascade.
Chemical communications (Cambridge, England), 2024, 60, 5691-5694
7133006 CIFC9 H19 F3 N2 O4 S2P 1 21/c 19.52; 8.588; 18.645
90; 99.465; 90
1503.6Nakazono, Yosuke; Inoue, Ryota; Sumitani, Ryo; Mochida, Tomoyuki
Solvent-free transformation of protic ionic liquids into zwitterions.
Chemical communications (Cambridge, England), 2024, 60, 5711-5714
7133007 CIFC9 H17 F3 N2 O4 S2P 1 21/c 18.664; 9.443; 17.044
90; 95.637; 90
1387.7Nakazono, Yosuke; Inoue, Ryota; Sumitani, Ryo; Mochida, Tomoyuki
Solvent-free transformation of protic ionic liquids into zwitterions.
Chemical communications (Cambridge, England), 2024, 60, 5711-5714
7133008 CIFC10 H16 F3 N3 O4 S2P -19.869; 17.149; 18.682
93.615; 92.206; 94.036
3145Nakazono, Yosuke; Inoue, Ryota; Sumitani, Ryo; Mochida, Tomoyuki
Solvent-free transformation of protic ionic liquids into zwitterions.
Chemical communications (Cambridge, England), 2024, 60, 5711-5714
7133009 CIFC45 H36 O9P b c m16.1779; 7.77835; 27.1947
90; 90; 90
3422.11Han, Ying; Guo, Wei-Chen; Du, Xu-Sheng; Chen, Chuan-Feng
Synthesis and properties of an <i>O</i>-doped aromatic belt.
Chemical communications (Cambridge, England), 2024, 60, 5719-5722
7133010 CIFC39 H18 O3P 1 21/n 111.4275; 15.9886; 16.0325
90; 97.391; 90
2904.96Han, Ying; Guo, Wei-Chen; Du, Xu-Sheng; Chen, Chuan-Feng
Synthesis and properties of an <i>O</i>-doped aromatic belt.
Chemical communications (Cambridge, England), 2024, 60, 5719-5722
7133011 CIFC58 H41 N3P 21 21 2112.7061; 14.0855; 23.6488
90; 90; 90
4232.5Sharma, Priyank Kumar; Jana, Palash; Bandyopadhyay, Subhajit; Das, Soumyajit
Cyano disubstituted tetrabenzoindeno[2,1-<i>a</i>]fluorene: open-shell or closed-shell?
Chemical communications (Cambridge, England), 2024, 60, 7319-7322
7133012 CIFC27 H42 N4 O5 SiP 1 21/c 112.838; 15.169; 15.0877
90; 102.909; 90
2863.91Jeanmard, Laksamee; Lodovici, Giacomo; George, Ian; Bray, Joshua T. W.; Whitwood, Adrian C.; Thomas, Gavin H.; Fairlamb, Ian J. S.; Unsworth, William P.; Clarke, Paul A.
Stereoselective synthesis of an advanced <i>trans</i>-decalin intermediate towards the total synthesis of anthracimycin.
Chemical communications (Cambridge, England), 2024, 60, 5699-5702
7133013 CIFC17 H22 O5P 21 21 217.18006; 12.9367; 17.2317
90; 90; 90
1600.59Jeanmard, Laksamee; Lodovici, Giacomo; George, Ian; Bray, Joshua T. W.; Whitwood, Adrian C.; Thomas, Gavin H.; Fairlamb, Ian J. S.; Unsworth, William P.; Clarke, Paul A.
Stereoselective synthesis of an advanced <i>trans</i>-decalin intermediate towards the total synthesis of anthracimycin.
Chemical communications (Cambridge, England), 2024, 60, 5699-5702
7133014 CIFC94 H150 Mg N4 Ni2 O8P -110.3314; 12.155; 20.115
85.509; 76.039; 68.417
2279.4Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133015 CIFC67 H100 Mg N4 Ni O4P -111.7869; 13.1585; 21.6061
95.572; 101.159; 101.843
3184.9Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133016 CIFC86 H133 Ca N5 Ni2 O12P -113.1189; 18.636; 19.149
81.507; 86.676; 74.077
4451.9Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133017 CIFC96 H158 Mg N4 Ni2 O8P 1 21/c 128.041; 14.697; 24.348
90; 104.01; 90
9736Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133018 CIFC92 H150 Ca N4 Ni2 O12P 1 n 116.7438; 14.268; 20.0197
90; 97.276; 90
4744.2Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133019 CIFC18 H14 Cl N OP 1 21/c 17.8569; 16.8285; 11.212
90; 104.254; 90
1436.81Sachin, ?; Sharma, Tamanna; Chandra, Devesh; Sumit, ?; Sharma, Upendra
Inherent directing group-enabled Co(III)-catalyzed C-H allylation/vinylation of isoquinolones.
Chemical communications (Cambridge, England), 2024, 60, 5626-5629
7133020 CIFC62 H47 Cl3 N6 O10 P2 Ru2P 1 21/c 119.7908; 15.1911; 23.1446
90; 107.604; 90
6632.4Arya, Yogita; Ansari, Toufik; Bera, Sudip Kumar; Panda, Sanjib; Indra, Arindam; Lahiri, Goutam Kumar
Superior electrocatalytic hydrogen evolution activity of a triply bridged diruthenium(II) complex on a carbon cloth support.
Chemical communications (Cambridge, England), 2024, 60, 6011-6014
7133021 CIFC24 H12 Br4 N6I 1 2/a 111.9288; 6.8445; 27.4989
90; 90.376; 90
2245.15Arya, Yogita; Ansari, Toufik; Bera, Sudip Kumar; Panda, Sanjib; Indra, Arindam; Lahiri, Goutam Kumar
Superior electrocatalytic hydrogen evolution activity of a triply bridged diruthenium(II) complex on a carbon cloth support.
Chemical communications (Cambridge, England), 2024, 60, 6011-6014
7133022 CIFC56 H41 Br3 Cl4 N4 O6 P2 RuP 1 21/c 118.3915; 14.4654; 20.9301
90; 100.804; 90
5469.55Arya, Yogita; Ansari, Toufik; Bera, Sudip Kumar; Panda, Sanjib; Indra, Arindam; Lahiri, Goutam Kumar
Superior electrocatalytic hydrogen evolution activity of a triply bridged diruthenium(II) complex on a carbon cloth support.
Chemical communications (Cambridge, England), 2024, 60, 6011-6014
7133023 CIFC58 H49 Cl N4 O6 P2 RuP -115.601; 21.105; 22.1703
110.152; 101.134; 99.661
6502.66Arya, Yogita; Ansari, Toufik; Bera, Sudip Kumar; Panda, Sanjib; Indra, Arindam; Lahiri, Goutam Kumar
Superior electrocatalytic hydrogen evolution activity of a triply bridged diruthenium(II) complex on a carbon cloth support.
Chemical communications (Cambridge, England), 2024, 60, 6011-6014
7133024 CIFC40 H46 Cd N0.5 O17.5 S4P 1 21/n 110.722; 39.433; 14.317
90; 97; 90
6008Su, Jian; Han, Xiao; Ke, Si-Wen; Zhou, Xiao-Cheng; Yuan, Shuai; Ding, Mengning; Zuo, Jing-Lin
Construction of a stable radical hydrogen-bonded metal-organic framework with functionalized tetrathiafulvalene linkers.
Chemical communications (Cambridge, England), 2024, 60, 5812-5815
7133025 CIFC43 H59 B N4 SiP -19.474; 13.9943; 16.2737
90.635; 90.829; 106.097
2072.54Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133026 CIFC57 H67 B N4 O2 SiP 1 21/n 112.9587; 24.1745; 16.8361
90; 103.559; 90
5127.2Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133027 CIFC69 H75 B N4 O2 SiC 1 c 111.765; 23.8074; 23.7692
90; 97.721; 90
6597.3Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133028 CIFC43 H59 B Ge N4P -19.5039; 14.0108; 16.3294
90.542; 90.684; 106.025
2089.55Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133029 CIFC86 H118 B2 N8 O2 Si2P 1 21/n 113.5861; 20.8352; 14.9701
90; 100.035; 90
4172.7Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133030 CIFC48 H59 B F5 N5 SiP 1 21/c 119.2831; 10.4515; 24.172
90; 103.424; 90
4738.5Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133031 CIFCs6 Na3 Nd O54 W10P -111.3552; 15.4905; 16.9027
101.371; 104.424; 91.701
2813.17Colliard, Ian; Deblonde, Gauthier J.-P.
Characterization of the first Peacock-Weakley polyoxometalate containing a transplutonium element: curium bis-pentatungstate [Cm(W<sub>5</sub>O<sub>18</sub>)<sub>2</sub>]<sup>9</sup>.
Chemical communications (Cambridge, England), 2024, 60, 5999-6002
7133032 CIFCm Cs8 Na O50 W10P -111.46121; 14.46007; 17.5536
101.11; 99.4298; 103.293
2711.36Colliard, Ian; Deblonde, Gauthier J.-P.
Characterization of the first Peacock-Weakley polyoxometalate containing a transplutonium element: curium bis-pentatungstate [Cm(W<sub>5</sub>O<sub>18</sub>)<sub>2</sub>]<sup>9</sup>.
Chemical communications (Cambridge, England), 2024, 60, 5999-6002
7133033 CIFC33 H26 N4 O6P 1 21/c 112.5972; 10.0613; 21.8687
90; 90.553; 90
2771.6Zhu, Shugao; Huang, Wenliang; Liu, Shihan; Yu, Rongjing; Ma, Yufeng; Wang, Hong; Zhang, Rui; Liu, Bin; Lan, Yu; Shen, Ruwei
Synthesis of benzooxepane-fused cyclobutene derivatives <i>via</i> Pd-catalyzed cascade reactions of haloarenes and diynylic ethers.
Chemical communications (Cambridge, England), 2024, 60, 5707-5710
7133034 CIFC42 H68 O8P 1 21 16.1621; 11.6465; 13.7206
90; 102.517; 90
961.28Rivera, Mario E.; Li, Lei; Kolisetti, Aditya; Chi, Nina; Dai, Mingji
9-Step synthesis of (-)-larikaempferic acid methyl ester enabled by skeletal rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7164-7167
7133035 CIFC21 H34 O4P 21 21 216.9015; 11.1195; 24.8315
90; 90; 90
1905.6Rivera, Mario E.; Li, Lei; Kolisetti, Aditya; Chi, Nina; Dai, Mingji
9-Step synthesis of (-)-larikaempferic acid methyl ester enabled by skeletal rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7164-7167
7133036 CIFC21 H34 O4I 1 2 120.0209; 6.9482; 29.3036
90; 107.026; 90
3897.74Rivera, Mario E.; Li, Lei; Kolisetti, Aditya; Chi, Nina; Dai, Mingji
9-Step synthesis of (-)-larikaempferic acid methyl ester enabled by skeletal rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7164-7167
7133037 CIFC23 H28 F3 N O8 SP 1 21 112.4612; 10.5196; 20.4828
90; 107.749; 90
2557.22Moore, Jonathan C.; Modell, Louis; Glenn, Jacqueline R.; Jones, Kieran D.; Argent, Stephen P.; Lane, J. Robert; Canals, Meritxell; Lam, Hon Wai
Enantioselective <i>de novo</i> synthesis of 14-hydroxy-6-oxomorphinans.
Chemical communications (Cambridge, England), 2024, 60, 6007-6010
7133038 CIFC23 H28 F3 N O8 SP 1 21 111.0308; 11.6724; 11.0847
90; 116.773; 90
1274.22Moore, Jonathan C.; Modell, Louis; Glenn, Jacqueline R.; Jones, Kieran D.; Argent, Stephen P.; Lane, J. Robert; Canals, Meritxell; Lam, Hon Wai
Enantioselective <i>de novo</i> synthesis of 14-hydroxy-6-oxomorphinans.
Chemical communications (Cambridge, England), 2024, 60, 6007-6010
7133039 CIFC19 H23 N O3P 1 21 110.163; 13.6943; 11.4184
90; 92.889; 90
1587.14Moore, Jonathan C.; Modell, Louis; Glenn, Jacqueline R.; Jones, Kieran D.; Argent, Stephen P.; Lane, J. Robert; Canals, Meritxell; Lam, Hon Wai
Enantioselective <i>de novo</i> synthesis of 14-hydroxy-6-oxomorphinans.
Chemical communications (Cambridge, England), 2024, 60, 6007-6010
7133040 CIFC19 H24 O2 SP 1 21/n 111.562; 5.6279; 26.4527
90; 92.458; 90
1719.7Suryawanshi, Sharad M.; Sahoo, Suman; Shaligram, Parth S.; Manna, Narugopal; Samanta, Ramesh C.
Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and <i>β</i>-dicarbonyls.
Chemical communications (Cambridge, England), 2024, 60, 5836-5839
7133041 CIFC16 H24 O2P c a 2110.399; 13.561; 9.888
90; 90; 90
1394.4Suryawanshi, Sharad M.; Sahoo, Suman; Shaligram, Parth S.; Manna, Narugopal; Samanta, Ramesh C.
Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and <i>β</i>-dicarbonyls.
Chemical communications (Cambridge, England), 2024, 60, 5836-5839
7133042 CIFC17 H18 O2P 1 21/c 111.0571; 10.1834; 11.8525
90; 102.1; 90
1304.93Suryawanshi, Sharad M.; Sahoo, Suman; Shaligram, Parth S.; Manna, Narugopal; Samanta, Ramesh C.
Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and <i>β</i>-dicarbonyls.
Chemical communications (Cambridge, England), 2024, 60, 5836-5839
7133043 CIFC12 H14 O4P 1 21/n 15.8827; 24.9167; 8.1339
90; 110.149; 90
1119.28Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiao-Bing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide.
Chemical communications (Cambridge, England), 2024, 60, 5735-5738
7133044 CIFC18 H18 O4P 1 21/n 15.845; 17.181; 7.9441
90; 107.273; 90
761.8Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiao-Bing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide.
Chemical communications (Cambridge, England), 2024, 60, 5735-5738
7133045 CIFC15 H16 O4P 1 21/c 110.828; 7.9485; 15.2171
90; 95.439; 90
1303.8Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiao-Bing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide.
Chemical communications (Cambridge, England), 2024, 60, 5735-5738
7133046 CIFC17 H18 O5P -15.8137; 8.5017; 16.6639
99.886; 92.872; 108.302
765.58Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiao-Bing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide.
Chemical communications (Cambridge, England), 2024, 60, 5735-5738
7133047 CIFC35 H15 B F15 N OP 1 21/n 110.78652; 21.7974; 17.9089
90; 105.265; 90
4062.15Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133048 CIFC29 H8 B F15 N2I 1 2/a 113.6313; 19.4305; 24.194
90; 99.003; 90
6329.1Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133049 CIFC35 H12 B F15 N4 O2P 1 21/c 112.0468; 16.3233; 15.715
90; 95.2169; 90
3077.45Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133050 CIFC30 H11 B Cl3 F15 N2C 1 2/c 134.981; 9.9268; 19.229
90; 109.205; 90
6305.7Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133051 CIFC27 H7 B F15 NP -111.505; 12.536; 17.074
77.759; 87.576; 77.117
2345.9Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133052 CIFC33 H11 B F15 NP -19.3635; 12.334; 13.652
108.894; 103.287; 96.811
1419.5Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133053 CIFC33 H11 B F15 NP -110.152; 10.204; 14.905
100.952; 99.276; 103.819
1437.1Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133054 CIFC38 H21 B F15 N3P 1 21/c 112.1553; 18.4902; 15.9842
90; 111.521; 90
3342.1Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133055 CIFC58.06 H70.12 Cl4.12 F4 I2 N6 O9 SeI 1 2/a 121.6338; 28.0204; 21.9354
90; 98.596; 90
13147.6Liu, Chuan-Zhi; Zhang, Chi; Li, Zhong-Yi; Chen, Jiale; Wang, Tonglu; Zhang, Xiang-Kun; Yan, Meng; Zhai, Bin
Multiple non-covalent-interaction-directed supramolecular double helices: the orthogonality of hydrogen, halogen and chalcogen bonding.
Chemical communications (Cambridge, England), 2024, 60, 6063-6066
7133056 CIFC32 H34 F3 I N4 O5 SeP -19.5768; 10.0412; 18.3416
96.6; 101.321; 98.752
1690.13Liu, Chuan-Zhi; Zhang, Chi; Li, Zhong-Yi; Chen, Jiale; Wang, Tonglu; Zhang, Xiang-Kun; Yan, Meng; Zhai, Bin
Multiple non-covalent-interaction-directed supramolecular double helices: the orthogonality of hydrogen, halogen and chalcogen bonding.
Chemical communications (Cambridge, England), 2024, 60, 6063-6066
7133057 CIFC56 H46 Cd2 N6 O10P 21 21 219.6443; 17.67; 36.653
90; 90; 90
6246.2Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.
Chemical communications (Cambridge, England), 2024, 60, 6182-6185
7133058 CIFC55 H42 Cd2 N6 O10P 21 21 219.6554; 17.7129; 36.6589
90; 90; 90
6269.6Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.
Chemical communications (Cambridge, England), 2024, 60, 6182-6185
7133059 CIFC45 H39 N4 O13 Zn4P 21 21 2113.6565; 29.6834; 14.1762
90; 90; 90
5746.6Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.
Chemical communications (Cambridge, England), 2024, 60, 6182-6185
7133060 CIFC45 H34 N4 O13 Zn4P 21 21 2113.6827; 14.1989; 29.77
90; 90; 90
5783.7Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.
Chemical communications (Cambridge, England), 2024, 60, 6182-6185
7133061 CIFC4 H6 Na O14 Re U2C 1 2/m 115.2417; 8.1267; 15.0583
90; 113.798; 90
1706.6Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133062 CIFC8 H12 Na2 O30 Tc2 U4C 1 2/m 115.2356; 8.1216; 15.0053
90; 114.061; 90
1695.39Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133063 CIFC4 H18 O32 Re2 U5P -17.7354; 8.4717; 12.782
94.029; 99.086; 109.92
770.66Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133064 CIFC4 H6 O32 Tc2 U5P -17.7451; 8.4501; 12.7565
93.982; 99.211; 109.708
768.96Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133065 CIFC8 H20 O25.75 Tc U4P b c n14.371; 13.8231; 14.8033
90; 90; 90
2940.7Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133066 CIFC13 H8 Br N SP 1 21/c 111.7154; 14.3463; 7.0036
90; 102.82; 90
1147.77Maeda, Bumpei; Akiyoshi, Ryohei; Tanaka, Daisuke; Sato, Kohei; Murakami, Kei
Synthesis of <i>N</i>-β-brominated alkenyl isothiocyanates <i>via</i> dehydrogenation of alkyl isothiocyanates.
Chemical communications (Cambridge, England), 2024, 60, 6015-6018
7133067 CIFC15 H10 Br N SP b c a7.4897; 18.6819; 19.2474
90; 90; 90
2693.13Maeda, Bumpei; Akiyoshi, Ryohei; Tanaka, Daisuke; Sato, Kohei; Murakami, Kei
Synthesis of <i>N</i>-β-brominated alkenyl isothiocyanates <i>via</i> dehydrogenation of alkyl isothiocyanates.
Chemical communications (Cambridge, England), 2024, 60, 6015-6018
7133068 CIFC36 H44 N4 O13 S3P 1 21 117.0638; 4.9924; 23.7104
90; 101.092; 90
1982.14Zhao, Chenyang; Li, Zujian; Ji, Lukang; Wang, Hanxiao; Ouyang, Guanghui; Liu, Minghua
Aggregate-state-dependent photochromism and circularly polarized luminescence of a chiral biquinoline amphiphile.
Chemical communications (Cambridge, England), 2024, 60, 6047-6050
7133069 CIFC26 H32 Br2.31 I1.69 N6 O2 ZnP -18.6011; 12.1473; 17.1881
71.236; 80.474; 79.466
1660.7Manna, Subarna; Sahoo, Sangita; Rit, Arnab
Synthesis of quinazolinone scaffolds <i>via</i> a zinc(II)-stabilized amidyl radical-promoted deaminative approach.
Chemical communications (Cambridge, England), 2024, 60, 7097-7100
7133070 CIFC107 H97 Cl3 O4P -110.8817; 15.6992; 25.2074
92.731; 92.591; 108.886
4061.44Hirano, Junichiro; Miyoshi, Sayaka; Yashima, Eiji; Ikai, Tomoyuki; Shinokubo, Hiroshi; Fukui, Norihito
Synthesis of sterically congested double helicene by alkyne cycloisomerization.
Chemical communications (Cambridge, England), 2024, 60, 6035-6038
7133071 CIFC11 H17 N O S2P 1 21/c 115.8974; 7.835; 9.4791
90; 100.682; 90
1160.2Cheng, Yuhe; Hyodo, Tadashi; Yamaguchi, Kentaro; Ohwada, Tomohiko; Otani, Yuko
Complete amide <i>cis</i>-<i>trans</i> switching synchronized with disulfide bond formation and cleavage in a proline-mimicking system.
Chemical communications (Cambridge, England), 2024, 60, 6158-6161
7133072 CIFC19 H20 N2 O4P -18.1324; 11.0134; 20.24
77.534; 79.396; 80.934
1726.67Liu, Zi; Greaney, Michael F.
Aminoarylation of alkynes using diarylanilines.
Chemical communications (Cambridge, England), 2024, 60, 6296-6299
7133073 CIFC15 H11 N SP -19.2993; 9.8997; 13.2708
82.308; 83.479; 77.987
1179.57George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133074 CIFC15 H11 N SP -19.2758; 9.9051; 13.2567
82.254; 83.462; 77.957
1175.69George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133075 CIFC15 H11 N SP -19.2177; 9.9216; 13.2043
82.062; 83.369; 77.928
1164.89George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133076 CIFC15 H11 N SP -19.1868; 9.9277; 13.1688
81.952; 83.305; 77.93
1158.19George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133077 CIFC15 H11 N SP -19.2356; 9.9171; 13.2232
82.118; 83.407; 77.923
1168.48George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133078 CIFC14 H11 N O S2P -19.6697; 10.5598; 13.8151
93.577; 100.035; 113.048
1264.85Wakabayashi, Ryota; Wang, Shuo; Kurogi, Takashi; Yorimitsu, Hideki
Arylation of benzazoles at the 4 positions by activation of their 2-methylsulfinyl groups.
Chemical communications (Cambridge, England), 2024, 60, 6166-6169
7133079 CIFC21 H16 N4 O5 Ru SP b c a10.1221; 16.1027; 25.1176
90; 90; 90
4094Yang, Jing; Zhan, Shaoqi; Wang, Linqin; Yang, Hao; Duan, Lele; Fan, Xiaolei; Liu, Tianqi; Sun, Licheng
Adaptive water oxidation catalysis on a carboxylate-sulfonate ligand with low onset potential.
Chemical communications (Cambridge, England), 2024, 60, 6162-6165
7133080 CIFC54 H58 B2 N6 O2 S2P 1 21/c 120.704; 6.2953; 18.9378
90; 108.615; 90
2339.2Fukami, Shuhei; Mori, Shigeki; Harada, Takunori; Shimizu, Soji
Far-red fluorescence and chiroptical properties of pyrrolopyrrole aza-BODIPYs induced by the <i>B</i>,<i>O</i>-chelation.
Chemical communications (Cambridge, England), 2024, 60, 6170-6173
7133081 CIFC38 H46 B2 F4 N6 S4P -17.7011; 11.6851; 11.8911
75.307; 71.596; 76.096
967.05Fukami, Shuhei; Mori, Shigeki; Harada, Takunori; Shimizu, Soji
Far-red fluorescence and chiroptical properties of pyrrolopyrrole aza-BODIPYs induced by the <i>B</i>,<i>O</i>-chelation.
Chemical communications (Cambridge, England), 2024, 60, 6170-6173
7133082 CIFC25 H22 Br N3 OP 1 21/c 15.946; 22.981; 16.1913
90; 96.653; 90
2197.56Fall, Arona; Magdei, Mihaela; Savchuk, Mariia; Oudeyer, Sylvain; Beucher, Hélène; Brière, Jean-François
Iron-catalyzed decarboxylative radical addition to chiral azomethine imines upon visible light.
Chemical communications (Cambridge, England), 2024, 60, 6316-6319
7133083 CIFC26 H25 N3 O2P 1 21/c 116.9362; 10.0156; 27.6433
90; 106.283; 90
4500.94Fall, Arona; Magdei, Mihaela; Savchuk, Mariia; Oudeyer, Sylvain; Beucher, Hélène; Brière, Jean-François
Iron-catalyzed decarboxylative radical addition to chiral azomethine imines upon visible light.
Chemical communications (Cambridge, England), 2024, 60, 6316-6319
7133084 CIFAl B3 Cl Cs O6P -3 c 17.0716; 7.0716; 18.0458
90; 90; 120
781.52Liu, Haoran; Jiao, Jiahao; Tudi, Abudukadi; Liu, Qingyu; Yang, Zhihua; Pan, Shilie; Zhang, Min
CsAlB<sub>3</sub>O<sub>6</sub>Cl: the rational construction of a KBBF-type structure with aligned <sup>2</sup><sub>∞</sub>[AlB<sub>3</sub>O<sub>6</sub>Cl] layers <i>via</i> introducing unprecedented [AlO<sub>3</sub>Cl] tetrahedra.
Chemical communications (Cambridge, England), 2024, 60, 6516-6519
7133085 CIFC6 I3 N PbP n m a7.8521; 11.3081; 15.9901
90; 90; 90
1419.8Möbs, Jakob; Tomori, Ajna; Heine, Johanna
Formation of iminium ions during the processing of metal halide perovskites.
Chemical communications (Cambridge, England), 2024, 60, 6488-6491
7133086 CIFC5 H12 I NI 4/m7.3846; 7.3846; 7.2299
90; 90; 90
394.263Möbs, Jakob; Tomori, Ajna; Heine, Johanna
Formation of iminium ions during the processing of metal halide perovskites.
Chemical communications (Cambridge, England), 2024, 60, 6488-6491
7133087 CIFC5 H12 I3 N PbP 63/m16.745; 16.745; 8.387
90; 90; 120
2036.6Möbs, Jakob; Tomori, Ajna; Heine, Johanna
Formation of iminium ions during the processing of metal halide perovskites.
Chemical communications (Cambridge, England), 2024, 60, 6488-6491
7133088 CIFC5 H12 I3 N PbP 63/m16.4064; 16.4064; 8.3883
90; 90; 120
1955.38Möbs, Jakob; Tomori, Ajna; Heine, Johanna
Formation of iminium ions during the processing of metal halide perovskites.
Chemical communications (Cambridge, England), 2024, 60, 6488-6491
7133089 CIFC84 H62 N2 O12 S8C 1 c 127.458; 23.377; 11.615
90; 90.454; 90
7455Du, Zhenglin; Xie, Jialin; Liu, Yandie; Tang, Yisong; Chen, Qing; Li, Xia; Zhu, Kelong
A π-extended molecular belt with selective binding capability for fullerene C<sub>70</sub>.
Chemical communications (Cambridge, England), 2024, 60, 6387-6390
7133090 CIFC142 H52 O8 S8P 1 21/n 117.1449; 33.6954; 21.4769
90; 92.559; 90
12394.9Du, Zhenglin; Xie, Jialin; Liu, Yandie; Tang, Yisong; Chen, Qing; Li, Xia; Zhu, Kelong
A π-extended molecular belt with selective binding capability for fullerene C<sub>70</sub>.
Chemical communications (Cambridge, England), 2024, 60, 6387-6390
7133091 CIFC30 H32 N2 O6P -110.405; 10.991; 12.216
109.33; 91.872; 104.146
1268.4Songsermsawad, Sarita; Shemchuk, Oleksii; Robeyns, Koen; Collard, Laurent; E Flood, Adrian; Leyssens, Tom
Simultaneously resolving BINOL and proline using a stoichiometric cocrystal switch.
Chemical communications (Cambridge, England), 2024, 60, 6607-6610
7133092 CIFC45 H37 N O6P 21 21 219.12901; 13.7793; 27.6456
90; 90; 90
3477.58Songsermsawad, Sarita; Shemchuk, Oleksii; Robeyns, Koen; Collard, Laurent; E Flood, Adrian; Leyssens, Tom
Simultaneously resolving BINOL and proline using a stoichiometric cocrystal switch.
Chemical communications (Cambridge, England), 2024, 60, 6607-6610
7133093 CIFC10 H20 Cu2 N5I b a m14.9083; 8.1008; 12.162
90; 90; 90
1468.79Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133094 CIFC10 H20 Cu2 N5I b a m14.8851; 8.1225; 12.2203
90; 90; 90
1477.49Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133095 CIFC10 H20 Cu2 N5I b a m14.7778; 8.2376; 12.5337
90; 90; 90
1525.77Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133096 CIFC10 H20 Cu2 N5I b a m14.8065; 8.2051; 12.4448
90; 90; 90
1511.9Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133097 CIFC10 H20 Cu2 N5I b a m14.8624; 8.1463; 12.2872
90; 90; 90
1487.66Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133098 CIFC10 H20 Cu2 N5I b a m14.8279; 8.1752; 12.366
90; 90; 90
1499.02Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133099 CIFC10 H20 Cu2 N5I b a m14.7531; 8.2731; 12.6466
90; 90; 90
1543.57Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133100 CIFC27 H17 N O3P b c a7.3843; 20.0427; 24.5666
90; 90; 90
3635.89Tanioka, Masaru; Mori, Minori; Harada, Mei; Matsuya, Yuji; Kamino, Shinichiro
Nonpolar selective emission (NPSE) of carbonyl-bridged rhodols.
Chemical communications (Cambridge, England), 2024, 60, 6407-6410
7133101 CIFC28 H16 F3 N O3P -110.994; 11.0404; 17.6631
83.512; 80.77; 72.972
2018.43Tanioka, Masaru; Mori, Minori; Harada, Mei; Matsuya, Yuji; Kamino, Shinichiro
Nonpolar selective emission (NPSE) of carbonyl-bridged rhodols.
Chemical communications (Cambridge, England), 2024, 60, 6407-6410
7133102 CIFC32 H19 N O3P b c a7.75825; 18.8157; 31.7145
90; 90; 90
4629.58Tanioka, Masaru; Mori, Minori; Harada, Mei; Matsuya, Yuji; Kamino, Shinichiro
Nonpolar selective emission (NPSE) of carbonyl-bridged rhodols.
Chemical communications (Cambridge, England), 2024, 60, 6407-6410
7133103 CIFC44 H32 Fe N10P -19.8316; 10.568; 17.2201
81.653; 83.058; 85.688
1754.2Sung, Yu-Shien; Tomat, Elisa
Quinoline-based tetrazolium prochelators: formazan release, iron sequestration, and antiproliferative efficacy in cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 6150-6153
7133104 CIFC26 H25 N O5P 21 21 215.0705; 19.7168; 21.861
90; 90; 90
2185.53Yang, Yang; Yang, Chenchen; Zhu, Xuefeng; Zhang, Li; Liu, Minghua
Interfacial self-assembly of a chiral pyrene exciplex into a superhelix with enhanced circularly polarized luminescence.
Chemical communications (Cambridge, England), 2024, 60, 6631-6634
7133105 CIFC68 H58 Cu2 N6 O16C 1 2/c 132.307; 14.1238; 16.6531
90; 97.426; 90
7535Saura-Sanmartin, Adrian; Cutillas-Font, Guillermo; Martinez-Cuezva, Alberto; Alajarin, Mateo; Esteban-Betegón, Fátima; Pena-Sánchez, Pilar; Gándara, Felipe; Berna, Jose
Mechanical bonding of rigid MORFs using a tetratopic rotaxane.
Chemical communications (Cambridge, England), 2024, 60, 6431-6434
7133106 CIFC68 H60 Co2 N6 O19P n m a16.795; 33.97; 13.8988
90; 90; 90
7929.6Saura-Sanmartin, Adrian; Cutillas-Font, Guillermo; Martinez-Cuezva, Alberto; Alajarin, Mateo; Esteban-Betegón, Fátima; Pena-Sánchez, Pilar; Gándara, Felipe; Berna, Jose
Mechanical bonding of rigid MORFs using a tetratopic rotaxane.
Chemical communications (Cambridge, England), 2024, 60, 6431-6434
7133107 CIFC33 H25 N OP -15.82; 9.093; 23.432
79.032; 87.963; 78.447
1192.7Yao, Yu-Xiang; Zhang, Jing; Min, Xuehong; Qin, Lan; Wei, Yi; Gao, Yang; Hu, Xiao-Qiang
Expedient access to polysubstituted acrylamides <i>via</i> strain-release-driven dual phosphine and palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6532-6535
7133108 CIFC35 H27 Cl2 N O2P 1 21/c 112.4215; 27.311; 9.588
90; 112.62; 90
3002.5Yao, Yu-Xiang; Zhang, Jing; Min, Xuehong; Qin, Lan; Wei, Yi; Gao, Yang; Hu, Xiao-Qiang
Expedient access to polysubstituted acrylamides <i>via</i> strain-release-driven dual phosphine and palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6532-6535
7133109 CIFC29 H23 N O3P 1 21/c 111.302; 22.17; 9.91
90; 107.88; 90
2363Yao, Yu-Xiang; Zhang, Jing; Min, Xuehong; Qin, Lan; Wei, Yi; Gao, Yang; Hu, Xiao-Qiang
Expedient access to polysubstituted acrylamides <i>via</i> strain-release-driven dual phosphine and palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6532-6535
7133110 CIFC27 H25 F3 O5 SP n a 2130.2694; 7.47312; 21.66
90; 90; 90
4899.64Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133111 CIFC25 H19 F3 O4 SC 1 c 17.3296; 14.8403; 19.798
90; 99.989; 90
2120.85Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133112 CIFC24 H19 B F4 OP 1 21/n 16.8567; 19.3806; 14.5799
90; 93.309; 90
1934.25Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133113 CIFC26 H19 F6 N O5 S2P -17.7877; 13.5269; 14.2246
115.433; 102.323; 95.02
1294.53Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133114 CIFC26 H19 F6 N O5 S2P -114.2426; 14.5647; 15.1706
117.808; 98.1608; 104.991
2558.64Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133115 CIFC17 H11 F3 N2 O4P -19.7758; 10.513; 11.2193
90.001; 112.552; 105.12
1021.51Wang, Manqing; Xu, Yuanshuang; Hou, Huihang; Zhang, Xinying; Fan, Xuesen
Divergent synthesis of pyrrolizine derivatives through C-H bond functionalization of pyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6536-6539
7133116 CIFC17 H15 F3 N2 O3P 1 21/c 110.9356; 17.2071; 9.5578
90; 113.916; 90
1644.07Wang, Manqing; Xu, Yuanshuang; Hou, Huihang; Zhang, Xinying; Fan, Xuesen
Divergent synthesis of pyrrolizine derivatives through C-H bond functionalization of pyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6536-6539
7133117 CIFC39 H50 N PP -110.7562; 13.4826; 14.1323
115.435; 107.508; 96.665
1692Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133118 CIFC33 H36 Br NP 1 21/c 110.4197; 14.0561; 18.9616
90; 100.363; 90
2731.82Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133119 CIFC109 H143 La2 N2 O P5P -115.498; 16.566; 22.288
76.309; 70.924; 69.957
5030.1Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133120 CIFC47 H69 K N O2 PP 1 21/n 111.463; 16.2623; 24.992
90; 97.374; 90
4620.3Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133121 CIFC164 H216 Cl10 K2 La4 N4 O2 P4P -112.833; 16.681; 21.1112
98.117; 100.137; 108.631
4120Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133122 CIFC85.6 H117 Cl La N2 O1.9 P2P 1 21/c 120.5986; 24.7411; 32.569
90; 95.767; 90
16514.2Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133123 CIFC11 H11 N9 OP 1 21/c 16.4786; 15.6097; 13.6164
90; 100.478; 90
1354.05Liu, Ziwei; Jiang, Clancy Zhijian; Bond, Andrew D.; Tosca, Nicholas J.; Sutherland, John D.
Manganese(II) promotes prebiotically plausible non-enzymatic RNA ligation reactions.
Chemical communications (Cambridge, England), 2024, 60, 6528-6531
7133124 CIFC46 H48 Br2 N2 O6 S4P -113.3806; 13.864; 15.8118
114.886; 90.41; 117.953
2272.67Li, Jia; Li, Liang; Mao, Mingming; Li, Rui-Peng; Huo, Xing; Tang, Shouchu
Site-selective synthesis of indanyl-substituted indole derivatives <i>via</i> 1,3-dithiane induced Nazarov cyclization.
Chemical communications (Cambridge, England), 2024, 60, 6540-6543
7133125 CIFC165 H129 Ce4 N39 O27P -122.747; 25.744; 26.168
82.095; 83.235; 63.886
13601Zhao, Lehua; Zhang, Yu; Wang, Huali; Wang, Jing; He, Cheng; Zhao, Liang; Duan, Chunying
Isolation of a copper photocatalyst on a metal-organic cage for the sulfonylation of aryl halides resulting from visible-light-mediated C(sp<sup>2</sup>)-S cross-coupling.
Chemical communications (Cambridge, England), 2024, 60, 6805-6808
7133126 CIFC27 H23 F Ge OP -19.8789; 11.0575; 11.8202
106.201; 104.242; 105.035
1124.69Lu, Xiao-Yu; Qian, Yu-Jun; Sun, Hai-Lun; Su, Meng-Xue; Wang, Zi-Zhen; Jiang, Fan; Zhou, Xin-Yue; Sun, Yan-Xi; Shi, Wan-Li; Wan, Ji-Ru
Photoinduced decarboxylative germylation of α-fluoroacrylic acids: access to germylated monofluoroalkenes.
Chemical communications (Cambridge, England), 2024, 60, 6556-6559
7133127 CIFC14 H16 N4 O5P 1 21/n 113.8775; 7.5913; 15.0147
90; 116.937; 90
1410.2Al Rahal, Okba; Ferguson, Michael; Lennox, Cameron B.; Male, Louise; Friščić, Tomislav
Structure of the caffeine-pyrogallol complex: revisiting a pioneering structural analysis of a model pharmaceutical cocrystal.
Chemical communications (Cambridge, England), 2024, 60, 7431-7434
7133128 CIFC14 H24 N4 O9P 42/n :223.1123; 23.1123; 6.8449
90; 90; 90
3656.4Al Rahal, Okba; Ferguson, Michael; Lennox, Cameron B.; Male, Louise; Friščić, Tomislav
Structure of the caffeine-pyrogallol complex: revisiting a pioneering structural analysis of a model pharmaceutical cocrystal.
Chemical communications (Cambridge, England), 2024, 60, 7431-7434
7133129 CIFC13 H16 Br2 N4 O3 WP 1 21/n 110.5949; 14.4051; 11.7972
90; 91.105; 90
1800.16Steiner, Lorenz; Ćorović, Miljan Z; Dupé, Antoine; Mösch-Zanetti, Nadia C
Vinyl-pyrazole as a biomimetic acetaldehyde surrogate.
Chemical communications (Cambridge, England), 2024, 60, 6873-6876
7133130 CIFC11 H12 Br2 Cl3 N3 O3 WP -19.2942; 10.3885; 11.1039
63.402; 75.498; 79.694
925.34Steiner, Lorenz; Ćorović, Miljan Z; Dupé, Antoine; Mösch-Zanetti, Nadia C
Vinyl-pyrazole as a biomimetic acetaldehyde surrogate.
Chemical communications (Cambridge, England), 2024, 60, 6873-6876
7133131 CIFC22 H30 Br Cl3 N6 O4 W2P 21 21 27.857; 15.9287; 12.3215
90; 90; 90
1542.06Steiner, Lorenz; Ćorović, Miljan Z; Dupé, Antoine; Mösch-Zanetti, Nadia C
Vinyl-pyrazole as a biomimetic acetaldehyde surrogate.
Chemical communications (Cambridge, England), 2024, 60, 6873-6876
7133132 CIFC15 H21 Br2 N5 O WP 1 21/c 111.3229; 8.0358; 21.4613
90; 95.852; 90
1942.56Steiner, Lorenz; Ćorović, Miljan Z; Dupé, Antoine; Mösch-Zanetti, Nadia C
Vinyl-pyrazole as a biomimetic acetaldehyde surrogate.
Chemical communications (Cambridge, England), 2024, 60, 6873-6876
7133133 CIFC15 H20 O5P -110.7822; 10.9047; 12.0558
88.037; 83.186; 89.353
1406.6Liu, Hongjian; Jiang, Huanfeng; Qi, Chaorong
Macrocyclization of carbon dioxide with 3-triflyloxybenzynes and tetrahydrofuran: straightforward access to 14-membered macrolactones.
Chemical communications (Cambridge, England), 2024, 60, 6639-6642
7133134 CIFC18 H23 F3 O7 SP 21 21 218.8302; 11.4492; 20.293
90; 90; 90
2051.6Liu, Hongjian; Jiang, Huanfeng; Qi, Chaorong
Macrocyclization of carbon dioxide with 3-triflyloxybenzynes and tetrahydrofuran: straightforward access to 14-membered macrolactones.
Chemical communications (Cambridge, England), 2024, 60, 6639-6642
7133135 CIFC24 H27 F3 O7 SP -113.4729; 13.6729; 14.874
65.885; 84.653; 77.547
2442Liu, Hongjian; Jiang, Huanfeng; Qi, Chaorong
Macrocyclization of carbon dioxide with 3-triflyloxybenzynes and tetrahydrofuran: straightforward access to 14-membered macrolactones.
Chemical communications (Cambridge, England), 2024, 60, 6639-6642
7133136 CIFC20 H30 OP -16.0028; 11.2789; 13.1074
64.982; 80.954; 87.69
793.83Dethe, Dattatraya H.; Sharma, Nitin; Juyal, Sakshi; Singh, Prabhakar; Siddiqui, Salman A.
Enantioselective total synthesis of atisane diterpenoids: (+)-sapinsigin H, (+)-agallochaol C, and (+)-16α, 17-dihydroxy-atisan-3-one.
Chemical communications (Cambridge, England), 2024, 60, 7866-7869
7133137 CIFC61 H92 Cr Li N4 O5P -112.3655; 14.1523; 19.2237
69.523; 76.232; 65.51
2850.94D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133138 CIFC62 H95 Cr Li N4 O5P -111.7699; 16.1506; 17.7227
97.669; 105.27; 108.783
2987.77D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133139 CIFC61 H90 Cr K N4 O8P -111.7863; 14.0237; 19.3145
85.096; 78.035; 75.843
3026.2D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133140 CIFC102 H140 Cr2 K2 N8 O5R -3 :H41.8744; 41.8744; 15.4776
90; 90; 120
23503.4D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133141 CIFC140 H202 Cr2 K2 N8 O17P -112.1161; 19.5547; 29.7051
82.767; 81.408; 78.704
6790.16D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133142 CIFC70 H63 B Cl3 F24 N2 O3 PP -112.6492; 13.6605; 21.8343
81.4; 78.136; 78.97
3600.1Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133143 CIFC149 H136 B2 F48 N4 O6 P2P -113.6399; 16.8477; 19.2953
115.857; 102.316; 98.273
3754.1Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133144 CIFC45 H60 Cl7 Ga2 N2 O3 PC 1 c 120.964; 12.2176; 20.1457
90; 93.743; 90
5148.9Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133145 CIFC86 H85 B F24 N5 O3 PP -112.1449; 18.623; 20.405
70.624; 73.911; 75.97
4125.1Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133146 CIFC91 H88 B F24 N2 O3 PP 1 21/n 113.9705; 31.6393; 19.2626
90; 93.898; 90
8494.7Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133147 CIFC89.36 H97.27 B F24 N2 O3 P SiP -113.1456; 17.6698; 20.0734
95.272; 103.875; 91.26
4502.8Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133148 CIFC79 H74 B F24 N2 O3 PP -113.9743; 16.814; 19.335
115.292; 106.112; 94.371
3845.7Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133149 CIFC79 H64 B F24 N2 O3 PP 1 21/c 112.366; 20.9073; 29.743
90; 97.228; 90
7628.6Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133150 CIFC28 H30 N2 O4C 1 c 114.4111; 20.2712; 10.3678
90; 129.444; 90
2338.94Sakai, Dan; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Stereoselective synthesis of 6/7/6-fused heterocycles with multiple stereocenters <i>via</i> an internal redox reaction/inverse electron-demand hetero-Diels-Alder reaction sequence.
Chemical communications (Cambridge, England), 2024, 60, 6797-6800
7133151 CIFC29 H32 Cl2 N2 O4P -19.9028; 11.7064; 11.8877
89.667; 74.086; 77.512
1291.8Sakai, Dan; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Stereoselective synthesis of 6/7/6-fused heterocycles with multiple stereocenters <i>via</i> an internal redox reaction/inverse electron-demand hetero-Diels-Alder reaction sequence.
Chemical communications (Cambridge, England), 2024, 60, 6797-6800
7133152 CIFC31 H46 F N S Si2P 1 21 18.1462; 13.1951; 15.8775
90; 96.946; 90
1694.15Zhou, Pengfei; Liang, Xinyao; Xu, Zekun; Chen, Honggu; Wei, Zongwu; Liang, Taoyuan; Jiang, Jun; Zhang, Zhuan
Regiodivergent C-H alkynylation of 2-arylthiazoles switched by Ru<sup>II</sup> and Pd<sup>II</sup> catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6679-6682
7133153 CIFC22 H29 N O S SiP -18.798; 12.4654; 21.0908
104.49; 90.974; 91.921
2237.4Zhou, Pengfei; Liang, Xinyao; Xu, Zekun; Chen, Honggu; Wei, Zongwu; Liang, Taoyuan; Jiang, Jun; Zhang, Zhuan
Regiodivergent C-H alkynylation of 2-arylthiazoles switched by Ru<sup>II</sup> and Pd<sup>II</sup> catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6679-6682
7133154 CIFC38 H39 N O8P 21 21 217.7775; 19.6476; 22.0751
90; 90; 90
3373.28Sun, Chunzhao; Inokuma, Tsubasa; Tsuji, Daisuke; Yamaoka, Yousuke; Akagi, Reiko; Yamada, Ken-Ichi
Total synthesis of 1,4a-di-<i>epi-ent</i>-pancratistatin, exemplifying a stereodivergent approach to pancratistatin isomers.
Chemical communications (Cambridge, England), 2024, 60, 6757-6760
7133155 CIFC51 H39 Cl2 N O13P 1 21 110.8258; 13.1828; 15.3126
90; 79.363; 90
2147.78Sun, Chunzhao; Inokuma, Tsubasa; Tsuji, Daisuke; Yamaoka, Yousuke; Akagi, Reiko; Yamada, Ken-Ichi
Total synthesis of 1,4a-di-<i>epi-ent</i>-pancratistatin, exemplifying a stereodivergent approach to pancratistatin isomers.
Chemical communications (Cambridge, England), 2024, 60, 6757-6760
7133156 CIFC6 H22 Br5 In N2 O2P n m a20.264; 7.9353; 11.0226
90; 90; 90
1772.4Biswas, Shuva; Mandal, Arnab; Swain, Diptikanta; Biswas, Kanishka
Synthesis and soft crystal structure-induced broad emission of (NH<sub>3</sub>C<sub>6</sub>H<sub>12</sub>NH<sub>3</sub>)InBr<sub>5</sub>·2H<sub>2</sub>O.
Chemical communications (Cambridge, England), 2024, 60, 7757-7760
7133157 CIFC6 H22 Br5 In N2 O2P 1 21/n 17.8333; 20.223; 10.9317
90; 91.232; 90
1731.3Biswas, Shuva; Mandal, Arnab; Swain, Diptikanta; Biswas, Kanishka
Synthesis and soft crystal structure-induced broad emission of (NH<sub>3</sub>C<sub>6</sub>H<sub>12</sub>NH<sub>3</sub>)InBr<sub>5</sub>·2H<sub>2</sub>O.
Chemical communications (Cambridge, England), 2024, 60, 7757-7760
7133158 CIFC18 H14 O2P 1 21/c 111.2312; 14.7726; 8.2671
90; 109.062; 90
1296.42Zhang, Xu; Chang, Mengfan; Xu, Xuefeng; Zhao, Qiang
Direct access to furan and cyclopropane derivatives <i>via</i> palladium-catalyzed C-H activation/alkene insertion/annulation.
Chemical communications (Cambridge, England), 2024, 60, 6769-6772
7133159 CIFC19 H19 N O4 SP 1 21/c 18.301; 11.0651; 18.7113
90; 93.468; 90
1715.51Li, Shuhui; Xu, Dan; Yao, Hui; Tan, Mengting; Li, Xiaoxuan; Liu, Mingguo; Wang, Long; Huang, Nianyu; Wang, Nengzhong
Facile synthesis of 2-vinylindolines <i>via</i> a phosphine-mediated α-umpolung/Wittig olefination/cyclization cascade process.
Chemical communications (Cambridge, England), 2024, 60, 6773-6776
7133160 CIFC27 H29 N O4 S2P 1 21/n 19.2418; 19.5215; 14.0366
90; 99.178; 90
2499.98Li, Shuhui; Xu, Dan; Yao, Hui; Tan, Mengting; Li, Xiaoxuan; Liu, Mingguo; Wang, Long; Huang, Nianyu; Wang, Nengzhong
Facile synthesis of 2-vinylindolines <i>via</i> a phosphine-mediated α-umpolung/Wittig olefination/cyclization cascade process.
Chemical communications (Cambridge, England), 2024, 60, 6773-6776
7133161 CIFC20 H21 N O5 SP -18.0093; 9.9303; 13.0524
92.274; 107.728; 106.033
941.63Li, Shuhui; Xu, Dan; Yao, Hui; Tan, Mengting; Li, Xiaoxuan; Liu, Mingguo; Wang, Long; Huang, Nianyu; Wang, Nengzhong
Facile synthesis of 2-vinylindolines <i>via</i> a phosphine-mediated α-umpolung/Wittig olefination/cyclization cascade process.
Chemical communications (Cambridge, England), 2024, 60, 6773-6776
7133162 CIFC12 H18 N2 O4C 1 2/c 123.2511; 6.0802; 18.4786
90; 97.79; 90
2588.2Shi, Lin; Liu, Lidong; Lei, Xingyu; Wang, Yihan; Fang, Yeguang; Jiao, Peng
Dearomative pyrrole (3+2) reaction with geminal bromonitroalkane: synthesis of 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6953-6956
7133163 CIFC18 H22 N2 O4P -19.5021; 9.6751; 10.0293
77.914; 71.586; 89.936
853.33Shi, Lin; Liu, Lidong; Lei, Xingyu; Wang, Yihan; Fang, Yeguang; Jiao, Peng
Dearomative pyrrole (3+2) reaction with geminal bromonitroalkane: synthesis of 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6953-6956
7133164 CIFC22 H29 N3 O5P -19.6012; 10.4718; 11.4984
86.861; 70.637; 79.609
1072.78Shi, Lin; Liu, Lidong; Lei, Xingyu; Wang, Yihan; Fang, Yeguang; Jiao, Peng
Dearomative pyrrole (3+2) reaction with geminal bromonitroalkane: synthesis of 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6953-6956
7133165 CIFC19 H22 N O4P 1 21/c 115.1005; 9.909; 11.5159
90; 93.934; 90
1719.1Shi, Lin; Liu, Lidong; Lei, Xingyu; Wang, Yihan; Fang, Yeguang; Jiao, Peng
Dearomative pyrrole (3+2) reaction with geminal bromonitroalkane: synthesis of 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6953-6956
7133166 CIFC32 H52 Bi2 F12 N4 Sb2C 1 2/c 136.971; 11.0199; 21.471
90; 101.205; 90
8581Sen, Nilanjana; Sarkar, Pallavi; Meena, Yadram; Tothadi, Srinu; Pati, Swapan K.; Khan, Shabana
Synthesis and catalytic application of a donor-free bismuthenium cation.
Chemical communications (Cambridge, England), 2024, 60, 6877-6880
7133167 CIFC93 H88 Ce4 N4P 1 21/c 18.0983; 17.5589; 27.1102
90; 90.172; 90
3854.98Gupta, Himanshu; Vincenzini, Brett D.; Bacon, Alexandra M.; Schelter, Eric J.
Assembly of a trapped valent Ce<sup>III/IV</sup>-TCNQ complex through metal-ligand redox cooperativity.
Chemical communications (Cambridge, England), 2024, 60, 6909-6912
7133168 CIFC7 H6 O2P 1 21/n 15.502; 5.137; 21.927
90; 97.045; 90
615.1Sun, Hainan; Li, Lili; Chen, Yahui; Kim, Yong Beom; Kim, Hyunseung; Fei, Liangshuang; Shao, Zongping; Jung, WooChul
Crystal structure optimization of copper oxides for the benzyl alcohol oxidation reaction.
Chemical communications (Cambridge, England), 2024, 60, 7224-7227
7133169 CIFC54 H53 N3P -110.502; 11.537; 19.141
96.877; 98.17; 99.193
2241.9Naniyil, Athira; Koroth Valappil, Naveen; Andrews, Alex P.; Gokulnath, Sabapathi
Carbazole-embedded <i>p</i>-benziporphyrinoid: synthesis, structure and a reversible chemodosimeter for mercury(II) ions.
Chemical communications (Cambridge, England), 2024, 60, 6957-6960
7133170 CIFC56 H54 Cl7 Hg N3R -3 :H43.456; 43.456; 14.847
90; 90; 120
24281Naniyil, Athira; Koroth Valappil, Naveen; Andrews, Alex P.; Gokulnath, Sabapathi
Carbazole-embedded <i>p</i>-benziporphyrinoid: synthesis, structure and a reversible chemodosimeter for mercury(II) ions.
Chemical communications (Cambridge, England), 2024, 60, 6957-6960
7133171 CIFC38 H53 Au N4 SiP -113.0228; 16.875; 18.996
76.362; 79.196; 70.713
3801.7Bakhoda, Abolghasem 'Gus'
Gold(I)-catalyzed homologation of aryl aldehydes with trimethylsilyldiazomethane.
Chemical communications (Cambridge, England), 2024, 60, 6937-6940
7133172 CIFC116.94 H127.44 Cl8.84 N12P -114.354; 18.2341; 23.2636
110.586; 101.322; 93.081
5538.9Heim, Gavin P.; Hirahara, Masanari; Dev, Vidhya M.; Agapie, Theodor
Synthesis and electronic properties of nitrogen-rich nanographene.
Chemical communications (Cambridge, England), 2024, 60, 7343-7346
7133173 CIFC25 H47 Ir P2P b c a10.0014; 17.1635; 28.5541
90; 90; 90
4901.6Demchuk, Mitchell J.; Zurakowski, Joseph A.; Drover, Marcus W.
Tridentate κ<sup>3</sup>-<i>P</i>,<i>P</i>,<i>C</i> iridium complexes: influence of ligand saturation on intramolecular C-H bond activation.
Chemical communications (Cambridge, England), 2024, 60, 7566-7569
7133174 CIFC25 H47 Ir P2P 1 21/c 110.405; 18.494; 13.748
90; 109.51; 90
2494Demchuk, Mitchell J.; Zurakowski, Joseph A.; Drover, Marcus W.
Tridentate κ<sup>3</sup>-<i>P</i>,<i>P</i>,<i>C</i> iridium complexes: influence of ligand saturation on intramolecular C-H bond activation.
Chemical communications (Cambridge, England), 2024, 60, 7566-7569
7133175 CIFC25 H49 Ir P2P b c a17.8681; 14.8775; 38.003
90; 90; 90
10102.4Demchuk, Mitchell J.; Zurakowski, Joseph A.; Drover, Marcus W.
Tridentate κ<sup>3</sup>-<i>P</i>,<i>P</i>,<i>C</i> iridium complexes: influence of ligand saturation on intramolecular C-H bond activation.
Chemical communications (Cambridge, England), 2024, 60, 7566-7569
7133176 CIFC5 H8 Cl F2 NP n m a10.0074; 7.0673; 9.5009
90; 90; 90
671.95Charlesworth, Natalie G.; Arunprasath, Dhanarajan; Graham, Mark A.; Argent, Stephen P.; Datsenko, Oleksandr P.; Mykhailiuk, Pavel K.; Denton, Ross M.
Modular synthesis of cyclic β-difluoroamines.
Chemical communications (Cambridge, England), 2024, 60, 7701-7704
7133177 CIFC29 H28 N0 O4C 1 2/c 119.9766; 15.8235; 15.6346
90; 93.935; 90
4930.4Ren, Yue; Shi, Wangyu; Tang, Yi; Guo, Hongchao
Phosphine-catalyzed (3+3) annulation of cinnamaldehyde-derived Morita-Baylis-Hillman carbonates with dinucleophiles.
Chemical communications (Cambridge, England), 2024, 60, 6897-6900
7133178 CIFC23 H18 N2 O5P 1 21/c 111.6492; 7.4491; 22.0277
90; 97.248; 90
1896.2He, Yongjun; He, Tian-Juan; Cheng, Xiufang; Wei, Yibo; Wang, Huamin; Lin, Ying-Wu
Phosphine-catalyzed dearomative [3+2] cycloaddition of 4-nitroisoxazoles with allenoates or Morita-Baylis-Hillman carbonates.
Chemical communications (Cambridge, England), 2024, 60, 6961-6964
7133179 CIFC15 H12 N4 O5 SP 1 21/c 113.0981; 11.5834; 10.0872
90; 100.284; 90
1505.85He, Yongjun; He, Tian-Juan; Cheng, Xiufang; Wei, Yibo; Wang, Huamin; Lin, Ying-Wu
Phosphine-catalyzed dearomative [3+2] cycloaddition of 4-nitroisoxazoles with allenoates or Morita-Baylis-Hillman carbonates.
Chemical communications (Cambridge, England), 2024, 60, 6961-6964
7133180 CIFC37 H39 B O2 SiC 1 2/c 116.206; 14.988; 26.246
90; 99.955; 90
6279Fujii, Ikuya; Hirata, Haruka; Moniwa, Hirokazu; Shintani, Ryo
Synthesis of (1-silyl)allylboronates by KO<i>t</i>Bu-catalyzed ring-opening <i>gem</i>-silylborylation of cyclopropenes.
Chemical communications (Cambridge, England), 2024, 60, 6921-6924
7133181 CIFC29 H46 Cr O2 P2P -110.4305; 10.4775; 14.5388
78.486; 83.946; 71.492
1474.9Duletski, Olivia L.; Platz, Duncan; Pollock, Charlie J.; Mosquera, Martín A; Arulsamy, Navamoney; Mock, Michael T.
Dinitrogen activation at chromium by photochemically induced Cr<sup>II</sup>-C bond homolysis.
Chemical communications (Cambridge, England), 2024, 60, 7029-7032
7133182 CIFC29 H46 Cr O2 P2P 1 21 18.2502; 15.8605; 11.8231
90; 106.188; 90
1485.74Duletski, Olivia L.; Platz, Duncan; Pollock, Charlie J.; Mosquera, Martín A; Arulsamy, Navamoney; Mock, Michael T.
Dinitrogen activation at chromium by photochemically induced Cr<sup>II</sup>-C bond homolysis.
Chemical communications (Cambridge, England), 2024, 60, 7029-7032
7133183 CIFC46 H83 Cr2 N2 O4.5 P4P 1 21/n 115.7583; 14.4111; 24.856
90; 107.974; 90
5369.2Duletski, Olivia L.; Platz, Duncan; Pollock, Charlie J.; Mosquera, Martín A; Arulsamy, Navamoney; Mock, Michael T.
Dinitrogen activation at chromium by photochemically induced Cr<sup>II</sup>-C bond homolysis.
Chemical communications (Cambridge, England), 2024, 60, 7029-7032
7133184 CIFC26 H21 N O4P 1 21 16.9055; 21.4299; 27.6189
90; 92.031; 90
4084.6Wang, Tao; Lu, Zhongyue; Li, Pengfei
Catalyst-free reaction of 2-(4<i>H</i>-benzo[<i>d</i>][1,3]oxazin-4-yl)acrylates: synthesis of 1,2-dihydroquinolines and 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6933-6936
7133185 CIFC24 H21 Cl N2 O3P -19.6896; 10.1998; 10.8323
89.99; 71.675; 84.875
1011.78Wang, Tao; Lu, Zhongyue; Li, Pengfei
Catalyst-free reaction of 2-(4<i>H</i>-benzo[<i>d</i>][1,3]oxazin-4-yl)acrylates: synthesis of 1,2-dihydroquinolines and 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6933-6936
7133186 CIFC34 H30 N2 O3P 1 21/c 111.847; 18.1061; 13.0266
90; 95.964; 90
2779.1Wang, Tao; Lu, Zhongyue; Li, Pengfei
Catalyst-free reaction of 2-(4<i>H</i>-benzo[<i>d</i>][1,3]oxazin-4-yl)acrylates: synthesis of 1,2-dihydroquinolines and 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6933-6936
7133187 CIFC10 H11 N O3P 1 21/c 19.9227; 5.672; 16.1656
90; 99.498; 90
897.35Winter, Johannes; Lühr, Susan; Hochadel, Kyra; Gálvez-Vázquez, María de Jesús; Prenzel, Tobias; Schollmeyer, Dieter; Waldvogel, Siegfried R.
Simple electrochemical synthesis of cyclic hydroxamic acids by reduction of nitroarenes.
Chemical communications (Cambridge, England), 2024, 60, 7065-7068
7133188 CIFC81 H106 N2 O18P 1 21/c 112.3241; 33.684; 20.229
90; 96.013; 90
8351Li, Bin; Wang, Yun; Wang, Yuan; Liu, Yue; Wang, Lu; Zhang, Zhi-Yuan; Li, Chunju
Vapochromic separation of toluene and pyridine azeotropes using adaptive macrocycle co-crystals.
Chemical communications (Cambridge, England), 2024, 60, 6889-6892
7133189 CIFC93 H110 N6 O14P -112.08; 12.4509; 29.1324
94.272; 92.465; 106.74
4174.8Li, Bin; Wang, Yun; Wang, Yuan; Liu, Yue; Wang, Lu; Zhang, Zhi-Yuan; Li, Chunju
Vapochromic separation of toluene and pyridine azeotropes using adaptive macrocycle co-crystals.
Chemical communications (Cambridge, England), 2024, 60, 6889-6892
7133190 CIFC52 H76 Fe N2 O2P -19.5346; 13.1604; 18.8315
91.84; 90.463; 91.367
2361Kulathungage, Lakshani W.; Kurup, Sudheer S.; Browne, Edison A.; Spalink, Gabriel H.; Ward, Cassandra L.; Lord, Richard L.; Groysman, Stanislav
Efficient carbene transfer reactivity mediated by Fe(II) complexes supported by bulky alkoxides.
Chemical communications (Cambridge, England), 2024, 60, 7033-7036
7133191 CIFC37 H28 O8P 1 21/c 110.323; 19.0774; 8.7024
90; 114.576; 90
1558.56Kulathungage, Lakshani W.; Kurup, Sudheer S.; Browne, Edison A.; Spalink, Gabriel H.; Ward, Cassandra L.; Lord, Richard L.; Groysman, Stanislav
Efficient carbene transfer reactivity mediated by Fe(II) complexes supported by bulky alkoxides.
Chemical communications (Cambridge, England), 2024, 60, 7033-7036
7133192 CIFC5 H6 O4P -15.006; 7.2628; 8.6451
106.71; 102.405; 92.116
292.37Kulathungage, Lakshani W.; Kurup, Sudheer S.; Browne, Edison A.; Spalink, Gabriel H.; Ward, Cassandra L.; Lord, Richard L.; Groysman, Stanislav
Efficient carbene transfer reactivity mediated by Fe(II) complexes supported by bulky alkoxides.
Chemical communications (Cambridge, England), 2024, 60, 7033-7036
7133193 CIFC26.9 H40.71 Cl6.1 Ga2 N4 O P PtP -18.30726; 15.0654; 15.9963
70.9877; 84.8936; 79.8892
1862.28Govindarajan, R.; Vardhanapu, Pavan K.; Fayzullin, Robert R.; Khaskin, Eugene; Khusnutdinova, Julia R.
Facile methyl group transfer from Pt<sup>II</sup> to gallium and indium.
Chemical communications (Cambridge, England), 2024, 60, 7216-7219
7133194 CIFC27 H41 Cl6 In2 N4 O P PtP 1 21/n 18.88651; 12.2296; 35.1991
90; 93.5845; 90
3817.9Govindarajan, R.; Vardhanapu, Pavan K.; Fayzullin, Robert R.; Khaskin, Eugene; Khusnutdinova, Julia R.
Facile methyl group transfer from Pt<sup>II</sup> to gallium and indium.
Chemical communications (Cambridge, England), 2024, 60, 7216-7219
7133195 CIFC28.77 H41.3 Cl6.23 In2 N4 O P PtP -18.71612; 14.4778; 17.6581
65.9038; 81.2608; 73.8299
1951.78Govindarajan, R.; Vardhanapu, Pavan K.; Fayzullin, Robert R.; Khaskin, Eugene; Khusnutdinova, Julia R.
Facile methyl group transfer from Pt<sup>II</sup> to gallium and indium.
Chemical communications (Cambridge, England), 2024, 60, 7216-7219
7133196 CIFC28 H22 N O2 PP -19.2305; 9.3886; 15.0613
83.016; 81.79; 62.191
1140.4Liu, Yong; Jia, Mengying; Wang, Guodong; Yang, Wenhui; Xu, Xianxiu
Silver-catalyzed P-centered anion nucleophilic addition to isocyanide: access to 2-phosphinoyl indoles/indol-3-ols.
Chemical communications (Cambridge, England), 2024, 60, 7196-7199
7133197 CIFC29 H24 N O3 PP -110.1021; 10.6285; 12.0861
95.272; 112.661; 92.657
1187.71Liu, Yong; Jia, Mengying; Wang, Guodong; Yang, Wenhui; Xu, Xianxiu
Silver-catalyzed P-centered anion nucleophilic addition to isocyanide: access to 2-phosphinoyl indoles/indol-3-ols.
Chemical communications (Cambridge, England), 2024, 60, 7196-7199
7133198 CIFC29.6 H25.2 Cl1.2 N O3 PP -19.9338; 11.4115; 13.4261
91.104; 99.247; 107.898
1425.68Liu, Yong; Jia, Mengying; Wang, Guodong; Yang, Wenhui; Xu, Xianxiu
Silver-catalyzed P-centered anion nucleophilic addition to isocyanide: access to 2-phosphinoyl indoles/indol-3-ols.
Chemical communications (Cambridge, England), 2024, 60, 7196-7199
7133199 CIFC46 H41 N2 O8 S2P -110.581; 10.781; 20.524
88.303; 85.635; 63.604
2091.1Bhati, Kuldeep Singh; Sharma, Siddharth
Electrochemically-driven difunctionalization of the isocyanide and Mumm rearrangement cascade: expeditious synthesis of <i>N</i>-acyl-<i>N</i>-alkyl <i>S</i>-thiocarbamates.
Chemical communications (Cambridge, England), 2024, 60, 7355-7358
7133200 CIFC26 H19 Cl F6 N2 O4P b c n16.652; 14.997; 21.13
90; 90; 90
5276.8Tang, Yong-Xing; Zhou, You; Wu, Hao-Xuan; Wang, Li-Sheng; Wu, Chun-Yan; Zhuang, Shi-Yi; Wu, An-Xin
<i>N</i>-Benzylhydroxylamine as a novel synthetic block in "C1N1" embedding reaction <i>via</i> α-C(sp<sup>3</sup>)-H activation strategy.
Chemical communications (Cambridge, England), 2024, 60, 7180-7183
7133201 CIFC15 H13 N O2C 1 2/c 112.719; 13.852; 14.156
90; 97.096; 90
2475Tang, Yong-Xing; Zhou, You; Wu, Hao-Xuan; Wang, Li-Sheng; Wu, Chun-Yan; Zhuang, Shi-Yi; Wu, An-Xin
<i>N</i>-Benzylhydroxylamine as a novel synthetic block in "C1N1" embedding reaction <i>via</i> α-C(sp<sup>3</sup>)-H activation strategy.
Chemical communications (Cambridge, England), 2024, 60, 7180-7183
7133202 CIFC38 H28 O3 P2P b c a16.51047; 16.41081; 23.08005
90; 90; 90
6253.54Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133203 CIFC19 H13 P SC 1 2/c 114.248; 13.5359; 15.8127
90; 90.772; 90
3049.35Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133204 CIFC24 H22 N O PP n a 2117.3159; 9.40206; 12.4887
90; 90; 90
2033.22Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133205 CIFC19 H13 P SeC 1 2/c 114.1963; 13.7375; 15.8281
90; 90.897; 90
3086.4Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133206 CIFC26 H20 N O2 P SP 1 21/c 18.19512; 13.942; 19.4641
90; 99.7093; 90
2192.04Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133207 CIFC34 H36 N O2 P SP 21 21 219.31097; 12.97197; 24.0692
90; 90; 90
2907.12Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133208 CIFC44 H33 B F4 N PP c a 2112.867; 13.069; 21.505
90; 90; 90
3616.3Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133209 CIFC25.5 H19 B Cl F3 N PP 1 21/c 19.5904; 16.0488; 14.2154
90; 101.406; 90
2144.74Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133210 CIFC31 H23 N O3 P2P 1 21/c 111.81181; 19.91502; 11.98573
90; 118.939; 90
2467.38Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133211 CIFC38 H28 O3 P2P b c a16.3712; 16.281; 22.9501
90; 90; 90
6117.11Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133212 CIFC19 H14 O2 PC 1 2/c 120.3958; 13.4454; 12.1945
90; 117.604; 90
2963.44Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133213 CIFC19 H13 P SeC 1 2/c 114.0369; 13.6803; 15.7202
90; 90.789; 90
3018.45Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133214 CIFC19 H13 O PP -17.2774; 8.0944; 13.1388
81.7506; 79.8049; 70.6319
715.63Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133215 CIFC25 H18 N PP 21 21 218.9413; 13.6176; 15.5673
90; 90; 90
1895.46Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133216 CIFC44 H20 B Cl2 F15 N PP -111.2365; 12.2624; 14.8185
83.39; 78.06; 74.601
1921.98Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133217 CIFC31 H30 N PP 1 21/n 19.0484; 18.306; 14.4219
90; 90.4144; 90
2388.78Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133218 CIFC27 H19 F6 N2 O4 P S2P -18.3718; 17.3368; 20.1621
113.925; 91.4063; 93.9353
2664.18Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133219 CIFC19 H13 P SC 1 2/c 114.0811; 13.4388; 15.6879
90; 90.464; 90
2968.57Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133220 CIFC27 H38 N2 O5 S SiP 1 21 18.956; 12.4093; 12.9018
90; 95.349; 90
1427.63Mroczyńska, Karina; Dobrzańska, Liliana; Rafiński, Zbigniew
Enantioselective synthesis of C3-functionalized 2,1-benzothiazine 2,2-dioxides by N-heterocyclic carbene catalysis.
Chemical communications (Cambridge, England), 2024, 60, 7176-7179
7133221 CIFC41 H35 Cl3 N0.5 O5 PP -111.7184; 12.545; 14.696
101.781; 98.985; 114.481
1853.15Zhou, Xiaocong; Wang, Jian; Ma, Dumei; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical synthesis of phosphorylated azaspiro[4.5]di/trienones through dearomative spirocyclization.
Chemical communications (Cambridge, England), 2024, 60, 7351-7354
7133222 CIFC58 H51.67 N2 O8 P2P b c a21.3419; 21.1766; 21.9827
90; 90; 90
9935.1Zhou, Xiaocong; Wang, Jian; Ma, Dumei; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical synthesis of phosphorylated azaspiro[4.5]di/trienones through dearomative spirocyclization.
Chemical communications (Cambridge, England), 2024, 60, 7351-7354
7133223 CIFC29 H24 Cl4 F N O2 PP -110.835; 12.7978; 20.779
81.75; 80.192; 89.486
2809.45Zhou, Xiaocong; Wang, Jian; Ma, Dumei; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical synthesis of phosphorylated azaspiro[4.5]di/trienones through dearomative spirocyclization.
Chemical communications (Cambridge, England), 2024, 60, 7351-7354
7133224 CIFC18 H13 N3 O2P -16.902; 13.8797; 16.3061
66.241; 89.878; 76.826
1385Chatterjee, Sarat; Khatun, Rousunara; Ali, Mahammad; Chowdhury, Chinmay
A solvent controlled regioselective synthesis of 2- and 4-substituted α-carbolines under palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 7427-7430
7133225 CIFC19 H16 N2P 1 21/n 113.4739; 7.1393; 14.6043
90; 101.576; 90
1376.27Chatterjee, Sarat; Khatun, Rousunara; Ali, Mahammad; Chowdhury, Chinmay
A solvent controlled regioselective synthesis of 2- and 4-substituted α-carbolines under palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 7427-7430
7133226 CIFC56 H92 Mg2 N4 O2 Si4P 1 21/n 115.637; 11.51056; 17.4414
90; 108.662; 90
2974.23O'Reilly, Andrea; Haynes, Matthew D.; Turner, Zoë R; McMullin, Claire L.; Harder, Sjoerd; O'Hare, Dermot; Fulton, J. Robin; Coles, Martyn P.
Mixing and matching <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO.
Chemical communications (Cambridge, England), 2024, 60, 7204-7207
7133227 CIFC42 H68 K Mg N2 O3 Si2P 1 21/n 114.3212; 20.5716; 15.38509
90; 94.3942; 90
4519.28O'Reilly, Andrea; Haynes, Matthew D.; Turner, Zoë R; McMullin, Claire L.; Harder, Sjoerd; O'Hare, Dermot; Fulton, J. Robin; Coles, Martyn P.
Mixing and matching <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO.
Chemical communications (Cambridge, England), 2024, 60, 7204-7207
7133228 CIFC66 H112 K2 Mg2 N4 O6 Si4P -110.9645; 15.9181; 23.3852
70.892; 89.038; 72.072
3653.33O'Reilly, Andrea; Haynes, Matthew D.; Turner, Zoë R; McMullin, Claire L.; Harder, Sjoerd; O'Hare, Dermot; Fulton, J. Robin; Coles, Martyn P.
Mixing and matching <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO.
Chemical communications (Cambridge, England), 2024, 60, 7204-7207
7133229 CIFC138 H224 K4 Mg4 N12 O4 Si8P -116.3939; 21.2191; 21.8811
81.3508; 89.9089; 88.1901
7521.29O'Reilly, Andrea; Haynes, Matthew D.; Turner, Zoë R; McMullin, Claire L.; Harder, Sjoerd; O'Hare, Dermot; Fulton, J. Robin; Coles, Martyn P.
Mixing and matching <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO.
Chemical communications (Cambridge, England), 2024, 60, 7204-7207
7133230 CIFC24 H18 O5P -18.3038; 11.289; 11.546
63.736; 87.201; 78.91
951.7Singh, Sanjay; Sharma, Pragya; Dutta, Sayantan; Vishwakarma, Rahul; Hazra, Chinmoy K.
An organocatalytic domino annulation approach <i>via</i> C(sp<sup>2</sup>)-OMe cleavage to unlock the synthesis of pyranochromenones enabled by HFIP.
Chemical communications (Cambridge, England), 2024, 60, 7200-7203
7133231 CIFC24 H17 Cl O5P -17.3859; 10.8372; 12.379
101.327; 97.246; 92.314
961.6Singh, Sanjay; Sharma, Pragya; Dutta, Sayantan; Vishwakarma, Rahul; Hazra, Chinmoy K.
An organocatalytic domino annulation approach <i>via</i> C(sp<sup>2</sup>)-OMe cleavage to unlock the synthesis of pyranochromenones enabled by HFIP.
Chemical communications (Cambridge, England), 2024, 60, 7200-7203
7133232 CIFC6 H36 Ho2 O30R -3 :H30.5; 30.5; 7.127
90; 90; 120
5742El Alouani Dahmouni, Nadia; Orts-Arroyo, Marta; Sanchis-Perucho, Adrián; Moliner, Nicolás; Mayans, Júlia; Pacheco, Mario; Castro, Isabel; De Munno, Giovanni; Marino, Nadia; Ruiz-García, Rafael; Martínez-Lillo, José
Magnetocaloric efficiency tuning through solvent-triggered 3D to 2D interconversion in holmium(III)-based dynamic MOFs.
Chemical communications (Cambridge, England), 2024, 60, 7451-7454
7133233 CIFC6 H20 Ho2 O22P 1 21/c 110.9347; 9.604; 9.9542
90; 114.143; 90
953.92El Alouani Dahmouni, Nadia; Orts-Arroyo, Marta; Sanchis-Perucho, Adrián; Moliner, Nicolás; Mayans, Júlia; Pacheco, Mario; Castro, Isabel; De Munno, Giovanni; Marino, Nadia; Ruiz-García, Rafael; Martínez-Lillo, José
Magnetocaloric efficiency tuning through solvent-triggered 3D to 2D interconversion in holmium(III)-based dynamic MOFs.
Chemical communications (Cambridge, England), 2024, 60, 7451-7454
7133234 CIFC21 H20 O4P 21 21 218.5423; 12.3659; 16.7686
90; 90; 90
1771.32Zeng, Hongkun; Wen, Gang; Lin, Lili; Feng, Xiaoming
Asymmetric dearomatization of benzyl 1-naphthyl ethers <i>via</i> [1,3] O-to-C rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7507-7510
7133235 CIFC55 H88 B2 Co F8 N4 O7P 1 21 112.6042; 16.7477; 13.9724
90; 90.008; 90
2949.45Zeng, Hongkun; Wen, Gang; Lin, Lili; Feng, Xiaoming
Asymmetric dearomatization of benzyl 1-naphthyl ethers <i>via</i> [1,3] O-to-C rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7507-7510
7133236 CIFC48 H96 Al4 Eu4 N8 O32I 1 2/a 127.7753; 10.2408; 29.891
90; 117.95; 90
7510.5Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133237 CIFC216 H440 Al16 Er16 N40 O136I 1 2/a 128.9871; 10.1594; 27.5988
90; 99.049; 90
8026.5Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133238 CIFC48 H96 Al4 N8 O32 Sm4I 1 2/a 127.9072; 10.2096; 29.8833
90; 118.087; 90
7511.7Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133239 CIFC47.99 H95.97 Al4 Gd4 N8 O32I 1 2/a 127.5463; 10.2945; 29.7052
90; 117.751; 90
7454.8Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133240 CIFC51 H103 Al4 Dy4 N9 O33I 1 2/a 129.1901; 10.2991; 27.6382
90; 98.946; 90
8207.8Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133241 CIFC51 H101 Al4 Ho4 N9 O33I 1 2/a 128.9677; 10.1285; 27.67
90; 99.14; 90
8015.3Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133242 CIFC48 H96 Al4 N8 O32 Tm4I 1 2/a 127.599; 10.1083; 28.8433
90; 99.182; 90
7943.6Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133243 CIFC54 H110 Al4 N10 O34 Tb4I 1 2/a 127.9239; 10.1329; 28.9993
90; 99.256; 90
8098.5Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133244 CIFC106 H92.03 N6 O18P -114.4561; 21.9459; 22.0092
60.305; 83.03; 74.276
5837.8Samanta, Krishanu; Mi, Jiashan; Chen, Albert D.; Li, Fangzhou; Staples, Richard J.; Rossini, Aaron J.; Ke, Chenfeng
Porous organic crystals crosslinked by free-radical reactions.
Chemical communications (Cambridge, England), 2024, 60, 7311-7314
7133245 CIFC102 H90 N6 O18P -114.3348; 21.7619; 21.9674
114.642; 97.609; 108.079
5642.86Samanta, Krishanu; Mi, Jiashan; Chen, Albert D.; Li, Fangzhou; Staples, Richard J.; Rossini, Aaron J.; Ke, Chenfeng
Porous organic crystals crosslinked by free-radical reactions.
Chemical communications (Cambridge, England), 2024, 60, 7311-7314
7133246 CIFC107 H98.1 N6 O18P -114.4122; 21.9201; 22.0159
60.357; 83.564; 74.23
5815.3Samanta, Krishanu; Mi, Jiashan; Chen, Albert D.; Li, Fangzhou; Staples, Richard J.; Rossini, Aaron J.; Ke, Chenfeng
Porous organic crystals crosslinked by free-radical reactions.
Chemical communications (Cambridge, England), 2024, 60, 7311-7314
7133247 CIFC144 H135 N9 O27C 1 2/c 138.116; 21.9306; 42.5599
90; 103.44; 90
34601.8Samanta, Krishanu; Mi, Jiashan; Chen, Albert D.; Li, Fangzhou; Staples, Richard J.; Rossini, Aaron J.; Ke, Chenfeng
Porous organic crystals crosslinked by free-radical reactions.
Chemical communications (Cambridge, England), 2024, 60, 7311-7314
7133248 CIFC12 H36 Ag Br11.74 Cl0.26 N4 SbP 1 c 18.6321; 7.8942; 25.961
90; 90.123; 90
1769.1Rajput, Shubham Ajaykumar; Antharjanam, Sudhadevi; Chandiran, Aravind Kumar
An above-room-temperature ferroelectric two-dimensional halide double perovskite with direction dependent properties.
Chemical communications (Cambridge, England), 2024, 60, 7898-7901
7133249 CIFC144 H290 Cu48 N16 O189 P16 S20C 1 2 132.3485; 19.7547; 32.5262
90; 112.66; 90
19180.9Teng, Qian; Gao, Ran; Bao, Song-Song; Zheng, Li-Min
Cu<sub>12</sub>-cluster-based metal-organic framework as a metastable intermediate in the formation of a layered copper phosphonate.
Chemical communications (Cambridge, England), 2024, 60, 7765-7768
7133250 CIFC9.5 H19 Cu2 N O10 P SP 21 21 217.0932; 7.3733; 31.2935
90; 90; 90
1636.66Teng, Qian; Gao, Ran; Bao, Song-Song; Zheng, Li-Min
Cu<sub>12</sub>-cluster-based metal-organic framework as a metastable intermediate in the formation of a layered copper phosphonate.
Chemical communications (Cambridge, England), 2024, 60, 7765-7768
7133251 CIFC34 H35 N3 O4 SP 1 21/c 114.791; 11.623; 18.6337
90; 109.354; 90
3022.4Sun, Zetian; Zhang, Jianting; Du, Xiaohua; Liu, Lulu; Gao, Shuo; Qi, Chenchen; Li, Xiaoqing; Xu, Xiangsheng
Photoinduced EnT-mediated sulfonamidylimination of alkenes and (hetero)arenes with iminophenylacetic acid oxime esters.
Chemical communications (Cambridge, England), 2024, 60, 7934-7937
7133252 CIFC61 H68 Cl2 O13R 3 c :H13.5991; 13.5991; 52.4778
90; 90; 120
8404.8Liu, Rui; Li, Ming; Liu, Zhongwen; Hua, Bin
Separation of cyclohexanol from cyclohexanol/cyclohexene mixtures by crystals of pillar[6]arene containing three benzoquinone units.
Chemical communications (Cambridge, England), 2024, 60, 7626-7629
7133253 CIFC39 H45 N3 O12P 1 21/c 116.1387; 28.3321; 8.3321
90; 95.419; 90
3792.8Wu, Simei; Tao, Wei; Wang, Tao; Xu, Jieqiong; Wei, Peifa
A crown ether embedded responsive π-gelator for transition from a one-component gel to a two-component gel.
Chemical communications (Cambridge, England), 2024, 60, 8232-8235
7133254 CIFC37 H41 N2 O12P 1 21/c 131.3061; 4.701; 26.9834
90; 93.029; 90
3965.6Wu, Simei; Tao, Wei; Wang, Tao; Xu, Jieqiong; Wei, Peifa
A crown ether embedded responsive π-gelator for transition from a one-component gel to a two-component gel.
Chemical communications (Cambridge, England), 2024, 60, 8232-8235
7133255 CIFC50 H36 O2P 1 21/n 117.155; 10.5253; 19.426
90; 91.508; 90
3506.4Sheokand, Sonu; Sharma, Sunita; Mohite, Manali A.; Rajaraman, Gopalan; Balakrishna, Maravanji S.
ZnCl<sub>2</sub>-catalysed transfer hydrogenation of carbonyls and chemoselective reduction of the CC bond in α,β-unsaturated ketones.
Chemical communications (Cambridge, England), 2024, 60, 7733-7736
7133256 CIFC48 H36 N2 O6 ZnP 1 21/c 17.9091; 23.3932; 20.4994
90; 90.281; 90
3792.74Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133257 CIFC48 H36 N2 O6 ZnP 1 21/c 17.9164; 23.6249; 20.5918
90; 91.802; 90
3849.3Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133258 CIFC48 H36 N2 O6 ZnP 1 21/c 17.8927; 23.5873; 20.5265
90; 91.988; 90
3819.1Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133259 CIFC48 H36 N2 O6 ZnP 1 21/c 17.8858; 23.506; 20.4093
90; 91.544; 90
3781.8Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133260 CIFC48 H36 N2 O6 ZnP 1 21/c 17.8902; 23.5724; 20.3308
90; 92.206; 90
3778.54Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133261 CIFC144 H212 K2 N2 O26 Ti2P -113.452; 22.8729; 23.7434
101.621; 94.411; 90.086
7133.5Ishida, Yutaka; Nakanishi, Yusuke; Hiratsuka, Takuma; Kawaguchi, Hiroyuki
Hydrazido complexes prepared by methylation of an anionic end-on bridging dinitrogen dititanium complex.
Chemical communications (Cambridge, England), 2024, 60, 7459-7462
7133262 CIFC108 H158 K2 N2 O10 Ti2C 1 c 113.92; 25.4342; 30.2821
90; 103.153; 90
10439.9Ishida, Yutaka; Nakanishi, Yusuke; Hiratsuka, Takuma; Kawaguchi, Hiroyuki
Hydrazido complexes prepared by methylation of an anionic end-on bridging dinitrogen dititanium complex.
Chemical communications (Cambridge, England), 2024, 60, 7459-7462
7133263 CIFC64 H64 N4P 1 21/n 112.6774; 23.2733; 17.2556
90; 92.162; 90
5087.6Jiang, Zhiyan; Kuninobu, Yoichiro
Synthesis of a novel twisted π-conjugated macrocycle <i>via</i> double Friedel-Crafts reaction and its physical properties.
Chemical communications (Cambridge, England), 2024, 60, 7642-7645
7133264 CIFC77 H61 Li8 N7 O19P -19.8956; 13.8451; 14.417
95.736; 94.844; 102.727
1905.5Li, Shu-Fan; Meng, Ya-Ru; Xu, Min-Jie; Zhang, Gen; Su, Jian
Construction of a redox-active metal-organic framework with an octanuclear lithium one-dimensional building block.
Chemical communications (Cambridge, England), 2024, 60, 8047-8050
7133265 CIFC136 H204 Ca4 N8 Zn4P -115.2503; 16.0371; 16.0776
69.051; 69.699; 71.172
3354.3Pearce, Kyle G.; Neale, Samuel E.; McMullin, Claire L.; Mahon, Mary F.; Hill, Michael S.
Pathway to a molecular calcium methyl.
Chemical communications (Cambridge, England), 2024, 60, 7882-7885
7133266 CIFC72 H116 Ca2 N4P 1 21/n 113.5951; 19.1092; 14.1535
90; 108.43; 90
3488.37Pearce, Kyle G.; Neale, Samuel E.; McMullin, Claire L.; Mahon, Mary F.; Hill, Michael S.
Pathway to a molecular calcium methyl.
Chemical communications (Cambridge, England), 2024, 60, 7882-7885
7133267 CIFC48 H31 Cl2 NP -110.6735; 11.3393; 15.9814
96.998; 104.429; 106.09
1761.56Wang, Ru-Jia; Zheng, Fan; Liu, Xiao-Long; Wu, Yu-Lan; Jin, Jia-Ming; Li, Ze-Yan; Chen, Wen-Cheng; Huo, Yanping
A through-space charge transfer pyrene-based fluorophore with anti-quenching behavior for deep-blue organic light-emitting devices.
Chemical communications (Cambridge, England), 2024, 60, 7946-7949
7133268 CIFC20 H18 O4P 21 21 216.3415; 8.4205; 30.8465
90; 90; 90
1647.16Tan, Zheng; Yihuo, Aying; Wu, Zhao; Wang, Fei; Dong, Shunxi; Feng, Xiaoming
Concise synthesis of chiral γ-butenolides <i>via</i> an allylation/lactonization cascade reaction.
Chemical communications (Cambridge, England), 2024, 60, 7926-7929
7133269 CIFC79 H69.5 Cd F12 N8.5 O8 P2P 1 21/n 112.4369; 24.8732; 25.4913
90; 101.228; 90
7734.7Wang, Shih-Yu; Lin, Lin-Ting; Rani, Alisha; Lee, Guan-Sian; Chan, Yi-Tsu
Stepwise construction of a metallocatenane based on non-labile bis(terpyridine)-Cd<sup>II</sup> complexes.
Chemical communications (Cambridge, England), 2024, 60, 7914-7917
7133270 CIFC26 H28 B N3P 1 21/c 18.4111; 15.3474; 17.0335
90; 96.326; 90
2185.4Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133271 CIFC32 H33 B2 N3P -18.9434; 12.002; 13.5298
105.413; 90.951; 109.556
1310.34Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133272 CIFC34 H43 B2 N3P 1 21/n 111.6929; 17.5821; 14.6284
90; 104.319; 90
2914Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133273 CIFC26 H28 B2 F3 N3P c a 2113.4867; 12.7379; 13.3863
90; 90; 90
2299.7Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133274 CIFC32 H33 B2 Cl2 N3P -18.2484; 8.6731; 22.3744
81.768; 85.754; 62.036
1399.1Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133275 CIFC26 H28 B2 Cl3 N3P 1 21/c 115.6649; 11.3864; 15.8645
90; 115.787; 90
2547.9Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133276 CIFC27 H31 B I N3P 1 21/c 18.0398; 28.378; 11.9315
90; 108.797; 90
2577Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133277 CIFC94 H162 Be2 Cl2 Li2 N4 O14 Si4P 1 21/c 121.4089; 22.319; 22.5227
90; 102.668; 90
10499.9Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394

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