Crystallography Open Database

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7132955 CIFC43 H43 N2 O2P 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 CIFC43 H43 N2 O2P 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 CIFC21 H34 O4P 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

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