Crystallography Open Database

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Searching journal of publication like 'Chemical communications (Cambridge, England)' volume of publication is 60

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7133408 CIFC10 H7 F3 O2P 1 21 18.51; 4.956; 11.481
90; 106.91; 90		463.3Kazi, Ayazoddin Aunoddin; Manjuladevi, Nadimpalli; Kumar, Salla Suresh; Sharma, Anamika; Singh, L. Ravithej
A quick access to CF<sub>3</sub>-containing functionalized benzofuranyl, benzothiophene and indolyl heterocycles under catalyst-free conditions.
Chemical communications (Cambridge, England), 2024, 60, 9376-9379
7133409 CIFC11 H9 Br F3 N O3 SP n a 215.4629; 21.481; 11.2799
90; 90; 90		1323.7Kazi, Ayazoddin Aunoddin; Manjuladevi, Nadimpalli; Kumar, Salla Suresh; Sharma, Anamika; Singh, L. Ravithej
A quick access to CF<sub>3</sub>-containing functionalized benzofuranyl, benzothiophene and indolyl heterocycles under catalyst-free conditions.
Chemical communications (Cambridge, England), 2024, 60, 9376-9379
7133410 CIFC161.8 H256.4 Br10 N10 O37P 1 21/c 126.50453; 14.53119; 25.82392
90; 114.266; 90		9067.12Gao, Tu-Nan; Yang, Zhen; Goed, Jesse M. S.; Zuilhof, Han; Miloserdov, Fedor M.
Rim-differentiated pillar[5]arene-modified surfaces for rapid PFOA/PFOS detection.
Chemical communications (Cambridge, England), 2024, 60, 9789-9792
7133411 CIFC21 H16 O3P 1 21 17.48375; 23.7768; 8.95801
90; 94.0554; 90		1589.99Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133412 CIFC44 H34 Br2 O4P 1 21/c 128.1188; 7.6926; 15.6637
90; 92.223; 90		3385.61Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133413 CIFC20 H13 Br O2P 21 21 218.0085; 8.9848; 21.0224
90; 90; 90		1512.66Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133414 CIFC21 H15 Br OP b c a15.1076; 10.0376; 20.6682
90; 90; 90		3134.2Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133415 CIFC21 H15 Br O2P 1 21 18.8697; 22.6968; 8.963
90; 114.336; 90		1644.05Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133416 CIFC22 H17 Br OP 21 21 215.595; 10.2307; 29.7158
90; 90; 90		1700.96Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133417 CIFC23 H21 Br O SiP 21 21 218.6383; 12.6159; 17.6123
90; 90; 90		1919.39Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133418 CIFC21 H15 Br OP 21 21 217.8805; 11.2373; 17.8564
90; 90; 90		1581.28Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133419 CIFC27 H19 Br OP 1 21 18.7121; 8.882; 13.2952
90; 98.023; 90		1018.72Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133420 CIFC22 H17 Br OP 21 21 217.6693; 13.0042; 17.0867
90; 90; 90		1704.11Li, Kai; Zhao, Zhengxing; Qin, Wenling; Liu, Yidong; Yan, Hailong
Catalytic asymmetric construction of bridged bicyclo[<i>m</i>.3.1] rings using an intramolecular Diels-Alder reaction.
Chemical communications (Cambridge, England), 2024, 60, 9570-9573
7133421 CIFC27 H18 Br N OP 21 21 218.151; 12.057; 19.765
90; 90; 90		1942Liu, Zi-Li; Wang, Yu-Xin; Yang, Zi-Qi; Yang, Yu-Heng; Liu, Yin-Ping; Hao, Wen-Juan; Jiang, Bo
Construction of central and axial chirality <i>via</i> Pd(II)/Bim-catalyzed asymmetric dearomative Michael reaction of polycyclic tropones.
Chemical communications (Cambridge, England), 2024, 60, 8908-8911
7133422 CIFC58 H62 N4 O2.5P -112.2185; 12.7948; 16.259
95.049; 93.58; 102.198		2466.2Nanda, Gyana Prakash; Chand, Savita; Rajamanickam, Suresh; Rajamalli, Pachaiyappan
Single-component TADF gels: study of the positional isomer effect on gelation and morphological effect on conductivity.
Chemical communications (Cambridge, England), 2024, 60, 9234-9237
7133423 CIFC24 H30 B PP -19.6433; 10.8253; 10.9474
75.97; 65.639; 70.947		976.29Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133424 CIFC23 H28 B PP 21 21 217.1446; 12.0021; 21.825
90; 90; 90		1871.5Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133425 CIFC26 H37 B2 O PP -19.1755; 11.3395; 12.5538
78.769; 77.719; 67.258		1167.84Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133426 CIFC19 H36 B PP b c a15.2898; 12.3183; 19.1817
90; 90; 90		3612.8Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133427 CIFC29 H53.5 Au B Cl N2 O0.75 PP -17.1927; 11.9175; 19.131
78.6195; 86.0612; 86.5573		1602.04Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133428 CIFC56 H102 B2 N4 O0.5 P2 PtP -110.6781; 10.9251; 12.9656
101.27; 98.789; 90.25		1465.06Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133429 CIFC20 H38 B PP 1 21/c 113.62; 10.375; 13.264
90; 93.932; 90		1869.9Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133430 CIFC26 H46 B N2 PP -111.1805; 11.2066; 11.5832
69.782; 80.362; 74.668		1308.78Hoffmann, Kurt F.; Noriega, Rayni P.; Boyle, Paul D.; Drover, Marcus W.
2-Alkylphosphino-1-boraadamantanes.
Chemical communications (Cambridge, England), 2024, 60, 9222-9225
7133431 CIFC15 H11 B F3 N OP 1 21/n 19.3925; 12.469; 11.765
90; 106.136; 90		1323.6Panigrahi, Pritishree; Ghosh, Subhendu; Khandelia, Tamanna; Tripathi, Gyanesh; Mandal, Raju; Patel, Bhisma K.
Harnessing reductive BF<sub>2</sub>-complexation <i>via</i> Ru(II)-catalyzed N-O cleavage of isoxazoles.
Chemical communications (Cambridge, England), 2024, 60, 9109-9112
7133432 CIFC18 H14 F N O2P -19.277; 9.5602; 9.7665
104.289; 110.312; 107.388		713.26Zhang, Jinhui; Mao, Lihua; Liu, Chao; Tan, Xiangwen; Wu, Jiahao; Wei, Xuefeng; Wu, Wanqing; Jiang, Huanfeng
Palladium-catalyzed 1,1-aminoxylation of 3-butenoic acid with 2-alkynylanilines.
Chemical communications (Cambridge, England), 2024, 60, 9404-9407
7133433 CIFC18 H19 N3 O4P 1 21/c 111.6692; 12.8126; 11.3946
90; 97.665; 90		1688.42Husbands, David R.; Booth, Elisha M.; Donaldson, Niall W. B.; Kapur, Nikil; Willans, Rebecca M.; Willans, Charlotte E.
Electrochemical removal of toxic metals from reaction media following catalysis.
Chemical communications (Cambridge, England), 2024, 60, 8876-8879
7133434 CIFC26 H31 Cl3 N6 OP 1 21/n 112.1807; 11.6269; 19.3144
90; 102.231; 90		2673.29Choi, Taehyeon; Kim, Heechan; Kim, Younghun; Lee, Dongwhan
Urea-fused and π-extended single-benzene fluorophores with ultralarge Stokes shifts.
Chemical communications (Cambridge, England), 2024, 60, 9105-9108
7133435 CIFC38 H44 F2 N2 O4P 1 21/c 18.6691; 21.3606; 18.6802
90; 99.169; 90		3414.9Roy, Barnali; Avasare, Vidya; Sarkar, Debayan
Tribromide enabled step-up generation of spirolactams from esters employing oxidative dearomatization of arenols.
Chemical communications (Cambridge, England), 2024, 60, 9206-9209
7133436 CIFC21 H17 N O4P 1 21/n 114.2969; 6.8015; 18.834
90; 112.036; 90		1697.6Meena, Shivam A.; Thakur, Deepika; Nandy, Abhijit; Ranjan, Rahul; Rai, Anubhav; Banerjee, Shibdas; Verma, Akhilesh K.
Transition-metal free, radical oxidation of 1,6-enyne cyclopropanation: synthesis of aza-bicyclo[4.1.0]heptane derivatives.
Chemical communications (Cambridge, England), 2024, 60, 9230-9233
7133437 CIFC19 H15 N O3P 1 21 110.275; 6.3644; 12.1715
90; 112.449; 90		735.63Meena, Shivam A.; Thakur, Deepika; Nandy, Abhijit; Ranjan, Rahul; Rai, Anubhav; Banerjee, Shibdas; Verma, Akhilesh K.
Transition-metal free, radical oxidation of 1,6-enyne cyclopropanation: synthesis of aza-bicyclo[4.1.0]heptane derivatives.
Chemical communications (Cambridge, England), 2024, 60, 9230-9233
7133438 CIFC18 H15 N O3P -110.6199; 10.8504; 15.1555
103.773; 97.032; 114.529		1493.92Meena, Shivam A.; Thakur, Deepika; Nandy, Abhijit; Ranjan, Rahul; Rai, Anubhav; Banerjee, Shibdas; Verma, Akhilesh K.
Transition-metal free, radical oxidation of 1,6-enyne cyclopropanation: synthesis of aza-bicyclo[4.1.0]heptane derivatives.
Chemical communications (Cambridge, England), 2024, 60, 9230-9233
7133439 CIFC22 H15 F N2P -18.757; 9.973; 11.506
103.314; 100.861; 113.664		850Zhou, Honggui; Li, Zhefeng; Chen, Juehong; Zhou, Si; Wang, Xinyu; Zhang, Linwei; Chen, Jiuxi; Lv, Ningning
Synthesis of polysubstituted pyridazines <i>via</i> Cu-mediated C(sp<sup>3</sup>)-C(sp<sup>3</sup>) coupling/annulation of saturated ketones with acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 9546-9549
7133440 CIFC70 H66 Li2 O2 P4 Se2P 1 21/c 115.7265; 9.5019; 20.4394
90; 97.157; 90		3030.5Duari, Prakash; Mondal, Sunita; Jörges, Mike; Gessner, Viktoria H.
The lithium effect in ketenyl anion chemistry.
Chemical communications (Cambridge, England), 2024, 60, 9372-9375
7133441 CIFC46 H66 Li2 N6 O2 P2 Se2C 1 2 123.832; 9.4158; 11.2461
90; 103.328; 90		2455.63Duari, Prakash; Mondal, Sunita; Jörges, Mike; Gessner, Viktoria H.
The lithium effect in ketenyl anion chemistry.
Chemical communications (Cambridge, England), 2024, 60, 9372-9375
7133442 CIFC70 H66 Li2 O2 P4 S2P 1 21/c 114.7042; 11.1057; 18.8325
90; 106.001; 90		2956.21Duari, Prakash; Mondal, Sunita; Jörges, Mike; Gessner, Viktoria H.
The lithium effect in ketenyl anion chemistry.
Chemical communications (Cambridge, England), 2024, 60, 9372-9375
7133443 CIFC36 H36 Li2 O6 P2P -114.2502; 15.4854; 15.5126
90.527; 91.99; 100.3		3365.56Duari, Prakash; Mondal, Sunita; Jörges, Mike; Gessner, Viktoria H.
The lithium effect in ketenyl anion chemistry.
Chemical communications (Cambridge, England), 2024, 60, 9372-9375
7133444 CIFC30 H33 B O2P 1 21/n 19.248; 12.097; 22.961
90; 100.211; 90		2528Sun, Fei; Zheng, Yiyi; Wu, Mingxia; Ji, Hongsen; Jiang, Zhongyao; Liu, Chenglin; Wu, Xin-Xing
Three-component cascade carbopalladation/Heck cyclization/borylation: facile access to boryl-functionalized indenes.
Chemical communications (Cambridge, England), 2024, 60, 8075-8078
7133445 CIFC31 H29 B F6 O2P -18.649; 13.234; 13.312
107.837; 95.839; 96.84		1424.7Sun, Fei; Zheng, Yiyi; Wu, Mingxia; Ji, Hongsen; Jiang, Zhongyao; Liu, Chenglin; Wu, Xin-Xing
Three-component cascade carbopalladation/Heck cyclization/borylation: facile access to boryl-functionalized indenes.
Chemical communications (Cambridge, England), 2024, 60, 8075-8078
7133446 CIFC48 H60 Br Cl4 N4 O2C 1 2/c 112.433; 20.341; 18.392
90; 90.85; 90		4650.8Song, Yuna; Song, Hayoung; Choi, Yunseop; Seo, Jongcheol; Lee, Eunsung
Synthesis of sterically congested unsymmetrical 1,2-dicarbonyl radicals through a stepwise approach.
Chemical communications (Cambridge, England), 2024, 60, 8043-8046
7133447 CIFC51 H62 Cl3 N4 O2P 1 21/n 110.837; 21.536; 22.074
90; 97.33; 90		5109.7Song, Yuna; Song, Hayoung; Choi, Yunseop; Seo, Jongcheol; Lee, Eunsung
Synthesis of sterically congested unsymmetrical 1,2-dicarbonyl radicals through a stepwise approach.
Chemical communications (Cambridge, England), 2024, 60, 8043-8046
7133448 CIFC38 H56 Cl N4 O3P 1 21/n 111.588; 18.52; 17.078
90; 92.11; 90		3662.6Song, Yuna; Song, Hayoung; Choi, Yunseop; Seo, Jongcheol; Lee, Eunsung
Synthesis of sterically congested unsymmetrical 1,2-dicarbonyl radicals through a stepwise approach.
Chemical communications (Cambridge, England), 2024, 60, 8043-8046
7133449 CIFC37 H54 Cl N4 O3P -111.704; 16.986; 19.521
87.59; 88.68; 81.55		3834.8Song, Yuna; Song, Hayoung; Choi, Yunseop; Seo, Jongcheol; Lee, Eunsung
Synthesis of sterically congested unsymmetrical 1,2-dicarbonyl radicals through a stepwise approach.
Chemical communications (Cambridge, England), 2024, 60, 8043-8046
7133450 CIFC51 H66 Cl N4 O3C 1 2/c 124.135; 22.011; 21.701
90; 122.41; 90		9733Song, Yuna; Song, Hayoung; Choi, Yunseop; Seo, Jongcheol; Lee, Eunsung
Synthesis of sterically congested unsymmetrical 1,2-dicarbonyl radicals through a stepwise approach.
Chemical communications (Cambridge, England), 2024, 60, 8043-8046
7133451 CIFC62 H51.35 N6 O6 S2P 110.2217; 11.1542; 13.1904
95.111; 94.018; 111.248		1387.58Choudhary, Kavita; Deshpande, Akanksha Santosh; Singh, Vinod K.
Ag(I)-catalyzed asymmetric (2+4) annulation reaction of 5-alkenyl thiazolones: synthesis of enantioenriched spiro[cyclohexenamines-thiazolones].
Chemical communications (Cambridge, England), 2024, 60, 9062-9065
7133452 CIFC40 H40 Cu I3 P2P 1 21/c 119.087; 13.1972; 17.36
90; 116.135; 90		3925.8Liu, Xia; Li, Bohan; Jin, Jiance; Yang, Lin; Xia, Zhiguo; Xu, Yan
Solvent-induced structural regulation and luminescence switching of hybrid copper(I) halides for encryption and anti-counterfeiting applications.
Chemical communications (Cambridge, England), 2024, 60, 9034-9037
7133453 CIFC20 H20 Cu I2 PP 1 21/c 18.679; 20.4707; 11.8536
90; 96.136; 90		2093.91Liu, Xia; Li, Bohan; Jin, Jiance; Yang, Lin; Xia, Zhiguo; Xu, Yan
Solvent-induced structural regulation and luminescence switching of hybrid copper(I) halides for encryption and anti-counterfeiting applications.
Chemical communications (Cambridge, England), 2024, 60, 9034-9037
7133454 CIFC20 H20 Cu3 I4 PP 1 21/c 112.7409; 25.0723; 7.9544
90; 106.194; 90		2440.16Liu, Xia; Li, Bohan; Jin, Jiance; Yang, Lin; Xia, Zhiguo; Xu, Yan
Solvent-induced structural regulation and luminescence switching of hybrid copper(I) halides for encryption and anti-counterfeiting applications.
Chemical communications (Cambridge, England), 2024, 60, 9034-9037
7133455 CIFC10 H10 Cl F OP 21 21 214.9064; 9.622; 19.4077
90; 90; 90		916.23He, Bin; Chen, Gen-Qiang; Zhang, Xumu
Highly efficient synthesis of enantioenriched vicinal halohydrins <i>via</i> Ir-catalyzed asymmetric hydrogenation using dynamic kinetic resolution.
Chemical communications (Cambridge, England), 2024, 60, 9785-9788
7133456 CIFC9 H8 Cl2 O2P 1 21 18.7032; 4.8645; 11.7272
90; 110.291; 90		465.68He, Bin; Chen, Gen-Qiang; Zhang, Xumu
Highly efficient synthesis of enantioenriched vicinal halohydrins <i>via</i> Ir-catalyzed asymmetric hydrogenation using dynamic kinetic resolution.
Chemical communications (Cambridge, England), 2024, 60, 9785-9788
7133457 CIFC20 H18 N4 O2P n a 2116.083; 19.232; 5.595
90; 90; 90		1731Maiti, Sandip; Parui, Nabin; Halder, Joydev; Dash, Jyotirmayee
Synthesis of triazole-fused tetracyclic spirooxindole derivatives <i>via</i> metal-free Huisgen cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 10009-10012

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