Crystallography Open Database

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7158520 CIFC3.43 H2.29 N0.29 O0.71 S0.14P 1 21/n 18.2185; 15.6692; 16.9546
90; 92.798; 90		2180.8Yao, Wen-Bo; Xie, Xuan-Sheng; Liu, Jun-Nan; Xie, Jian-Wu
Diversity-oriented and diastereoselective synthesis of diverse polycyclic thieno(2,3-<i>b</i>)-quinoline derivatives using a synergistic strategy.
Organic & biomolecular chemistry, 2022, 20, 1982-1993
7158522 CIFC10 H16 O5 SP 21 21 215.457; 10.698; 21.399
90; 90; 90		1249.3Chen, Wei-Li; Liu, Zhang-Wei; Wang, Ying-Chun; Ma, Xiao-Pan; Mo, Dong-Liang
MnSO<sub>4</sub>-promoted S-O bond cleavage for synthesizing functionalized sulfonium ylides from activated alkynes and sulfoxides.
Organic & biomolecular chemistry, 2022, 20, 1656-1661
7158523 CIFC26 H32 N2 O3P 1 21/n 19.1754; 19.184; 13.4902
90; 100.044; 90		2338.17Koványi-Lax, Györgyi; Hargitai, Csilla; Ábrányi-Balogh, Péter; Nagy, Tamás; Tóth, Gábor; Garádi, Zsófia; Németh, Gábor; Pandur, Angéla; Horváth, Simon; Dancsó, András; Simig, Gyula; Volk, Balázs
Experimental and computational study of BF<sub>3</sub>-catalyzed transformations of <i>ortho</i>-(pivaloylaminomethyl)benzaldehydes: an unexpected difference from TFA catalysis.
Organic & biomolecular chemistry, 2022, 20, 1933-1944
7158524 CIFC28 H32 N2 O7P b c a7.7233; 23.323; 30.276
90; 90; 90		5453.6Koványi-Lax, Györgyi; Hargitai, Csilla; Ábrányi-Balogh, Péter; Nagy, Tamás; Tóth, Gábor; Garádi, Zsófia; Németh, Gábor; Pandur, Angéla; Horváth, Simon; Dancsó, András; Simig, Gyula; Volk, Balázs
Experimental and computational study of BF<sub>3</sub>-catalyzed transformations of <i>ortho</i>-(pivaloylaminomethyl)benzaldehydes: an unexpected difference from TFA catalysis.
Organic & biomolecular chemistry, 2022, 20, 1933-1944
7158525 CIFC29 H42 O9P 1 21 114.8186; 6.1275; 17.0159
90; 103.869; 90		1500.02Ure, Elizabeth M.; Harris, Lawrence D.; Cameron, Scott A.; Weymouth-Wilson, Alex; Furneaux, Richard H.; Pitman, Janet L.; Hinkley, Simon F.; Luxenburger, Andreas
Synthesis of 12β-methyl-18-<i>nor</i>-avicholic acid analogues as potential TGR5 agonists.
Organic & biomolecular chemistry, 2022, 20, 3511-3527
7158526 CIFC24 H36 O5P 21 21 218.9657; 13.2198; 18.8147
90; 90; 90		2230.01Ure, Elizabeth M.; Harris, Lawrence D.; Cameron, Scott A.; Weymouth-Wilson, Alex; Furneaux, Richard H.; Pitman, Janet L.; Hinkley, Simon F.; Luxenburger, Andreas
Synthesis of 12β-methyl-18-<i>nor</i>-avicholic acid analogues as potential TGR5 agonists.
Organic & biomolecular chemistry, 2022, 20, 3511-3527
7158527 CIFC29 H44 O8P 21 21 219.97027; 13.27902; 20.904
90; 90; 90		2767.59Ure, Elizabeth M.; Harris, Lawrence D.; Cameron, Scott A.; Weymouth-Wilson, Alex; Furneaux, Richard H.; Pitman, Janet L.; Hinkley, Simon F.; Luxenburger, Andreas
Synthesis of 12β-methyl-18-<i>nor</i>-avicholic acid analogues as potential TGR5 agonists.
Organic & biomolecular chemistry, 2022, 20, 3511-3527
7158528 CIFC25 H46 O6P 21 21 217.4781; 12.81; 25.4104
90; 90; 90		2434.2Ure, Elizabeth M.; Harris, Lawrence D.; Cameron, Scott A.; Weymouth-Wilson, Alex; Furneaux, Richard H.; Pitman, Janet L.; Hinkley, Simon F.; Luxenburger, Andreas
Synthesis of 12β-methyl-18-<i>nor</i>-avicholic acid analogues as potential TGR5 agonists.
Organic & biomolecular chemistry, 2022, 20, 3511-3527
7158529 CIFC24 H36 O6P 21 21 220.4236; 11.2645; 10.8753
90; 90; 90		2501.99Ure, Elizabeth M.; Harris, Lawrence D.; Cameron, Scott A.; Weymouth-Wilson, Alex; Furneaux, Richard H.; Pitman, Janet L.; Hinkley, Simon F.; Luxenburger, Andreas
Synthesis of 12β-methyl-18-<i>nor</i>-avicholic acid analogues as potential TGR5 agonists.
Organic & biomolecular chemistry, 2022, 20, 3511-3527
7158530 CIFC24.19 H42.38 O7P 21 21 218.31799; 10.12992; 28.0673
90; 90; 90		2364.97Ure, Elizabeth M.; Harris, Lawrence D.; Cameron, Scott A.; Weymouth-Wilson, Alex; Furneaux, Richard H.; Pitman, Janet L.; Hinkley, Simon F.; Luxenburger, Andreas
Synthesis of 12β-methyl-18-<i>nor</i>-avicholic acid analogues as potential TGR5 agonists.
Organic & biomolecular chemistry, 2022, 20, 3511-3527
7158531 CIFC25 H42 O4P 6532.26794; 32.26794; 6.19392
90; 90; 120		5585.2Ure, Elizabeth M.; Harris, Lawrence D.; Cameron, Scott A.; Weymouth-Wilson, Alex; Furneaux, Richard H.; Pitman, Janet L.; Hinkley, Simon F.; Luxenburger, Andreas
Synthesis of 12β-methyl-18-<i>nor</i>-avicholic acid analogues as potential TGR5 agonists.
Organic & biomolecular chemistry, 2022, 20, 3511-3527
7158532 CIFC22 H15 Br F3 N O2 S SeP -19.0368; 9.7879; 12.8089
72.001; 83.06; 79.877		1058.06Wang, Hui; Yao, Yunfei; You, Yi; Huang, Yangjie; Weng, Zhiqiang
An aerobic copper-mediated domino process for the synthesis of 3-(trifluoromethylseleno)indoles.
Organic & biomolecular chemistry, 2022, 20, 2115-2120
7158576 CIFC18 H14 O3P -15.5942; 10.5681; 11.9447
102.226; 92.692; 90.534		689.26Krishna, Anugam V.; Ramachary, Dhevalapally B.
The seven-step, one-pot regioselective synthesis of biologically important 3-aryllawsones: scope and applications.
Organic & biomolecular chemistry, 2022, 20, 3948-3954
7158577 CIFC17 H12 O4P 1 21/c 110.4584; 3.9248; 31.2078
90; 95.455; 90		1275.19Krishna, Anugam V.; Ramachary, Dhevalapally B.
The seven-step, one-pot regioselective synthesis of biologically important 3-aryllawsones: scope and applications.
Organic & biomolecular chemistry, 2022, 20, 3948-3954
7158578 CIFC18 H14 O4P -15.442; 10.6713; 12.7912
71.516; 87.083; 75.865		682.89Krishna, Anugam V.; Ramachary, Dhevalapally B.
The seven-step, one-pot regioselective synthesis of biologically important 3-aryllawsones: scope and applications.
Organic & biomolecular chemistry, 2022, 20, 3948-3954
7158579 CIFC17 H12 O3P 1 21/n 112.3812; 5.5547; 18.6375
90; 94.036; 90		1278.59Krishna, Anugam V.; Ramachary, Dhevalapally B.
The seven-step, one-pot regioselective synthesis of biologically important 3-aryllawsones: scope and applications.
Organic & biomolecular chemistry, 2022, 20, 3948-3954
7158582 CIFC23 H22 Cl N O6P b c a14.998; 12.8933; 21.1475
90; 90; 90		4089.4Tang, Zhishun; Chen, Linghong; Yin, Pengxuan; Yang, Lu; Shi, Zhichuan; Zhao, Zhigang; Ye, Ling; Li, Xuefeng
Diastereoselective construction of tetracyclic chromanes <i>via</i> a triply annulative strategy.
Organic & biomolecular chemistry, 2022, 20, 3342-3347
7158590 CIFC30 H23 Cl N2 O3 SP 1 21/n 112.9731; 15.1155; 13.3582
90; 94.384; 90		2611.8Dai, Qing-Song; Li, Jun-Long; Wang, Qi-Wei; Yang, Si-Lin; Tao, Ying-Mao; He, Mei-Hao; Li, Qing-Zhu; Han, Bo; Zhang, Xiang
Sulphur ylide-mediated cyclopropanation and subsequent spirocyclopropane rearrangement reactions.
Organic & biomolecular chemistry, 2022, 20, 3486-3490
7158591 CIFC30 H22 N2 O3 SP n a 2121.023; 12.4076; 18.781
90; 90; 90		4898.9Dai, Qing-Song; Li, Jun-Long; Wang, Qi-Wei; Yang, Si-Lin; Tao, Ying-Mao; He, Mei-Hao; Li, Qing-Zhu; Han, Bo; Zhang, Xiang
Sulphur ylide-mediated cyclopropanation and subsequent spirocyclopropane rearrangement reactions.
Organic & biomolecular chemistry, 2022, 20, 3486-3490
7158592 CIFC28 H20 N2 O3 S2P -111.4722; 11.6024; 11.81
112.336; 91.537; 112.501		1315.8Dai, Qing-Song; Li, Jun-Long; Wang, Qi-Wei; Yang, Si-Lin; Tao, Ying-Mao; He, Mei-Hao; Li, Qing-Zhu; Han, Bo; Zhang, Xiang
Sulphur ylide-mediated cyclopropanation and subsequent spirocyclopropane rearrangement reactions.
Organic & biomolecular chemistry, 2022, 20, 3486-3490
7158594 CIFC16 H14 F3 N3 OP -18.1282; 13.2665; 14.8538
111.379; 101.712; 94.591		1439.47Lan, Jianyong; Li, Shaoyun; Lin, Kejun; Zhou, Peng; Chen, Weili; Gao, Liqian; Zhu, Tingshun
The eco-friendly electrosynthesis of trifluoromethylated spirocyclic indolines and their anticancer activity.
Organic & biomolecular chemistry, 2022, 20, 3475-3479
7158595 CIFC28 H24 F N O5 S2P 21 21 216.7215; 18.6021; 20.0805
90; 90; 90		2510.75Son, Yeri; Hwang, Sunjoo; Bak, Sujin; Kim, Ha Eun; Choi, Jun-Ho; Chung, Won-Jin
α-Fluoroamine synthesis <i>via</i> P(III)-mediated deoxygenative geminal fluorosulfonimidation of 1,2-diketones.
Organic & biomolecular chemistry, 2022, 20, 3263-3267
7158596 CIFC30 H24 Br N3 O7P c a 219.4017; 18.1121; 18.3977
90; 90; 90		3132.84Gu, Congzheng; Tian, Guangzheng; Yin, Qingyu; Wu, Fan; Li, Zhiming; Wu, Xiaoyu
Amide phosphonium salt catalyzed enantioselective Mannich addition of isoxazole-based nucleophiles to β,γ-alkynyl-α-ketimino esters.
Organic & biomolecular chemistry, 2022, 20, 3323-3334
7158611 CIFC21 H22 N2 O5P 1 21/c 15.7351; 41.9722; 8.3858
90; 107.644; 90		1923.63Hsu, Yin-Yin; Luo, Sheng-Qi; Hong, Bor-Cherng; Chien, Su-Ying
A mild one-pot transformation of nitroalkanes to ketones or aldehydes <i>via</i> a visible-light photocatalysis-hydrolysis sequence.
Organic & biomolecular chemistry, 2022, 20, 3292-3302
7158612 CIFC25 H15 F N2 O3P -17.147; 11.942; 12.279
61.56; 87.07; 75.58		889.7Yun, Ei Seul; Akhtar, Muhammad Saeed; Mohandoss, Sonaimuthu; Lee, Yong Rok
Microwave-assisted annulation for the construction of pyrido-fused heterocycles and their application as photoluminescent chemosensors.
Organic & biomolecular chemistry, 2022, 20, 3397-3407
7158616 CIFC25 H16 Cl Cu N5 O2P -18.1305; 9.2545; 14.7289
96.831; 98.583; 104.865		1044.74Das, Krishna Mohan; Pal, Adwitiya; Adarsh, Nayarassery N.; Thakur, Arunabha
A novel quinoline-based NNN-pincer Cu(II) complex as a superior catalyst for oxidative esterification of allylic C(sp<sup>3</sup>)-H bonds.
Organic & biomolecular chemistry, 2022, 20, 3540-3549
7158617 CIFC13 H14 O3P 1 21/c 110.881; 10.233; 11.017
90; 108.43; 90		1163.8Das, Krishna Mohan; Pal, Adwitiya; Adarsh, Nayarassery N.; Thakur, Arunabha
A novel quinoline-based NNN-pincer Cu(II) complex as a superior catalyst for oxidative esterification of allylic C(sp<sup>3</sup>)-H bonds.
Organic & biomolecular chemistry, 2022, 20, 3540-3549
7158618 CIFC17 H23 B Cl3 N O3C 1 c 18.8732; 23.4482; 10.733
90; 109.856; 90		2100.35Szwetkowski, Connor; Slebodnick, Carla; Santos, Webster L.
Regio- and stereoselective copper-catalyzed α,β-protoboration of allenoates: access to <i>Z</i>-β,γ-unsaturated β-boryl esters.
Organic & biomolecular chemistry, 2022, 20, 3287-3291
7158619 CIFC15 H27 N O4P 1 21 110.537; 10.802; 15.329
90; 94.978; 90		1738.2Auddy, Sourya Shankar; Saha, Sanu; Goswami, Rajib Kumar
Total synthesis and stereochemical assignment of bipolamide A acetate.
Organic & biomolecular chemistry, 2022, 20, 3348-3358
7158620 CIFC13 H25 N O5P 1 21 110.7002; 6.0652; 11.85
90; 99.659; 90		758.15Auddy, Sourya Shankar; Saha, Sanu; Goswami, Rajib Kumar
Total synthesis and stereochemical assignment of bipolamide A acetate.
Organic & biomolecular chemistry, 2022, 20, 3348-3358
7158621 CIFC7 H11 N O4P 21 21 215.466; 10.025; 15.193
90; 90; 90		832.5Auddy, Sourya Shankar; Saha, Sanu; Goswami, Rajib Kumar
Total synthesis and stereochemical assignment of bipolamide A acetate.
Organic & biomolecular chemistry, 2022, 20, 3348-3358
7158624 CIFC13 H17 B N5 O0.5I 1 2/a 113.1462; 8.7576; 25.691
90; 102.499; 90		2887.7Zhang, Yifei; Liao, Yangzhen; Liu, Peijun; Ran, Yu; Liu, Xiaozu
Radical borylation of vinyl azides with NHC-boranes: divergent synthesis of α-boryl ketones and borylated triazoles.
Organic & biomolecular chemistry, 2022, 20, 3550-3557
7158625 CIFC25.5 H17 Cl I N O2P 1 21 110.4688; 15.0424; 14.4588
90; 104.344; 90		2205.93Wang, Ying; Yang, Yang; Xu, Shiyu; Huang, Aima; Chen, Lu; Xie, Yubao; Liu, Pengyutian; Hong, Liang; Li, Guofeng
Organocatalytic enantioselective construction of axially chiral (1<i>H</i>)-isochromen-1-imines.
Organic & biomolecular chemistry, 2022, 20, 3277-3282
7158626 CIFC36 H22 Cl2 N4 O5P -18.346; 12.269; 14.899
92.2; 101.408; 92.387		1492.5Mandal, Rahul Dev; Saha, Moumita; Das, Asish R.
Accessing oxy-functionalized N-heterocycles through rose bengal and TBHP integrated photoredox C(sp<sup>3</sup>)-O cross-coupling.
Organic & biomolecular chemistry, 2022, 20, 2939-2963
7158627 CIFC36 H23 Br N4 O5P 1 21/n 113.543; 10.328; 22.564
90; 100.723; 90		3101Mandal, Rahul Dev; Saha, Moumita; Das, Asish R.
Accessing oxy-functionalized N-heterocycles through rose bengal and TBHP integrated photoredox C(sp<sup>3</sup>)-O cross-coupling.
Organic & biomolecular chemistry, 2022, 20, 2939-2963
7158628 CIFC14 H9 N O2P b c a11.6817; 7.6497; 23.7774
90; 90; 90		2124.8Mandal, Rahul Dev; Saha, Moumita; Das, Asish R.
Accessing oxy-functionalized N-heterocycles through rose bengal and TBHP integrated photoredox C(sp<sup>3</sup>)-O cross-coupling.
Organic & biomolecular chemistry, 2022, 20, 2939-2963
7158630 CIFC35 H26 Cl3 F3 N2 O5P 1 21/c 123.784; 18.643; 7.321
90; 90.762; 90		3245.9Fang, Zheng; Teng, Yun; Yang, Huilin; Li, Rongxing; Li, Qiuhong; You, Yi; Weng, Zhiqiang
Synthesis of 4-trifluoromethyl pyridazines <i>via</i> annulation of pyridinium ylides with trifluoroacetyl diazoester.
Organic & biomolecular chemistry, 2022, 20, 3564-3569
7158631 CIFC24 H13 F3 N6 O2P b c a15.582; 12.447; 22.472
90; 90; 90		4358.4Fang, Zheng; Teng, Yun; Yang, Huilin; Li, Rongxing; Li, Qiuhong; You, Yi; Weng, Zhiqiang
Synthesis of 4-trifluoromethyl pyridazines <i>via</i> annulation of pyridinium ylides with trifluoroacetyl diazoester.
Organic & biomolecular chemistry, 2022, 20, 3564-3569
7158632 CIFC22 H15 F3 N2 O4C 1 c 128.4017; 10.6516; 14.9143
90; 116.751; 90		4029Fang, Zheng; Teng, Yun; Yang, Huilin; Li, Rongxing; Li, Qiuhong; You, Yi; Weng, Zhiqiang
Synthesis of 4-trifluoromethyl pyridazines <i>via</i> annulation of pyridinium ylides with trifluoroacetyl diazoester.
Organic & biomolecular chemistry, 2022, 20, 3564-3569
7158636 CIFC8 H11 F N2 O4 SC 1 2/c 120.3525; 5.1265; 23.391
90; 111.209; 90		2275.2Yang, Wen-Fei; Shu, Tao; Chen, Hong-Ru; Qin, Hua-Li; Tang, Haolin
A cascade reaction for regioselective construction of pyrazole-containing aliphatic sulfonyl fluorides.
Organic & biomolecular chemistry, 2022, 20, 3506-3510
7158637 CIFC27 H18 N O4P -19.3467; 15.2593; 16.6257
66.179; 79.925; 88.526		2133.1Tan Uygun, Meltem; Menges, Nurettin
Synthesis of spiroindolenine-cyclopentenedione skeletons and their chemical behaviours: the first example of a lactone-type spiroindolenine structure.
Organic & biomolecular chemistry, 2022, 20, 4161-4166
7158640 CIFC24 H24 N4P 1 21/n 16.554; 12.6859; 23.2169
90; 97.357; 90		1914.4Stahlberger, M.; Steinlein, O.; Adam, C. R.; Rotter, M.; Hohmann, J.; Nieger, M.; Köberle, B; Bräse, S
Fluorescent annulated imidazo[4,5-<i>c</i>]isoquinolines <i>via</i> a GBB-3CR/imidoylation sequence - DNA-interactions in pUC-19 gel electrophoresis mobility shift assay.
Organic & biomolecular chemistry, 2022, 20, 3598-3604
7158641 CIFC19 H19 N5P 1 21/c 17.7193; 19.0741; 10.7854
90; 103.055; 90		1546.98Stahlberger, M.; Steinlein, O.; Adam, C. R.; Rotter, M.; Hohmann, J.; Nieger, M.; Köberle, B; Bräse, S
Fluorescent annulated imidazo[4,5-<i>c</i>]isoquinolines <i>via</i> a GBB-3CR/imidoylation sequence - DNA-interactions in pUC-19 gel electrophoresis mobility shift assay.
Organic & biomolecular chemistry, 2022, 20, 3598-3604
7158642 CIFC34 H28 N3 O3P -110.3432; 11.855; 12.43
79.657; 66.16; 74.86		1341Cheng, Ya-Long; Wu, Guoqing; Zang, Yong-Jun; Hu, Yuan-Yang; Qin, Lu-Zhe; Wen, Xiaoan; Xu, Qing-Long
Diversity synthesis of indole derivatives <i>via</i> catalyst control cyclization reaction of 2-indolylmethanols and azonaphthalene.
Organic & biomolecular chemistry, 2022, 20, 3930-3939
7158643 CIFC37 H35 N3 O4P 1 21/c 115.4317; 13.3076; 15.3933
90; 109.518; 90		2979.5Cheng, Ya-Long; Wu, Guoqing; Zang, Yong-Jun; Hu, Yuan-Yang; Qin, Lu-Zhe; Wen, Xiaoan; Xu, Qing-Long
Diversity synthesis of indole derivatives <i>via</i> catalyst control cyclization reaction of 2-indolylmethanols and azonaphthalene.
Organic & biomolecular chemistry, 2022, 20, 3930-3939
7158644 CIFC37 H33 N3 O3P -18.9864; 9.7311; 18.0784
78.844; 81.754; 75.67		1495.17Cheng, Ya-Long; Wu, Guoqing; Zang, Yong-Jun; Hu, Yuan-Yang; Qin, Lu-Zhe; Wen, Xiaoan; Xu, Qing-Long
Diversity synthesis of indole derivatives <i>via</i> catalyst control cyclization reaction of 2-indolylmethanols and azonaphthalene.
Organic & biomolecular chemistry, 2022, 20, 3930-3939
7158649 CIFC15 H19 N OP 21 21 217.1151; 8.4448; 21.3264
90; 90; 90		1281.41Takagi, Ryukichi; Tanimoto, Takaaki
Enantioselective [2 + 2] photocycloaddition of quinolone using a <i>C</i><sub>1</sub>-symmetric chiral phosphoric acid as a visible-light photocatalyst.
Organic & biomolecular chemistry, 2022, 20, 3940-3947
7158650 CIFC21 H26 Co N2 O5P -4 21 m20.4662; 20.4662; 5.0315
90; 90; 90		2107.52Ricca, Michael; Zhang, Wei; Li, Jiaqi; Fellowes, Thomas; White, Jonathan M.; Donnelly, Paul S.; Rizzacasa, Mark A.
Synthesis of acyloin natural products by Mukaiyama hydration.
Organic & biomolecular chemistry, 2022, 20, 4038-4047
7158651 CIFC17 H22 O5P -18.7844; 10.2193; 18.8935
75.495; 84.894; 88.497		1635.49Ricca, Michael; Zhang, Wei; Li, Jiaqi; Fellowes, Thomas; White, Jonathan M.; Donnelly, Paul S.; Rizzacasa, Mark A.
Synthesis of acyloin natural products by Mukaiyama hydration.
Organic & biomolecular chemistry, 2022, 20, 4038-4047
7158652 CIFC22 H30 N2 O5P -18.3632; 10.7798; 12.6342
67.34; 80.523; 88.594		1035.8Ricca, Michael; Zhang, Wei; Li, Jiaqi; Fellowes, Thomas; White, Jonathan M.; Donnelly, Paul S.; Rizzacasa, Mark A.
Synthesis of acyloin natural products by Mukaiyama hydration.
Organic & biomolecular chemistry, 2022, 20, 4038-4047
7158653 CIFC26 H31 Co N2 O6P 1 21/c 17.9465; 26.3631; 11.4522
90; 92.613; 90		2396.68Ricca, Michael; Zhang, Wei; Li, Jiaqi; Fellowes, Thomas; White, Jonathan M.; Donnelly, Paul S.; Rizzacasa, Mark A.
Synthesis of acyloin natural products by Mukaiyama hydration.
Organic & biomolecular chemistry, 2022, 20, 4038-4047
7158654 CIFC16 H21 N5 O3P 1 21/c 119.378; 4.9594; 18.3832
90; 116.058; 90		1587.1Edmonds, Anthony K.; Oakes, Catherine S.; Hassell-Hart, Storm; Bruyère, Didier; Tizzard, Graham J.; Coles, Simon J.; Felix, Robert; Maple, Hannah J.; Marsh, Graham P.; Spencer, John
Scale-up and optimization of the synthesis of dual CBP/BRD4 inhibitor ISOX-DUAL.
Organic & biomolecular chemistry, 2022, 20, 4021-4029
7158655 CIFC16 H19 N3 O3 SP -17.2068; 15.1888; 15.2406
74.263; 85.817; 76.699		1562.57Edmonds, Anthony K.; Oakes, Catherine S.; Hassell-Hart, Storm; Bruyère, Didier; Tizzard, Graham J.; Coles, Simon J.; Felix, Robert; Maple, Hannah J.; Marsh, Graham P.; Spencer, John
Scale-up and optimization of the synthesis of dual CBP/BRD4 inhibitor ISOX-DUAL.
Organic & biomolecular chemistry, 2022, 20, 4021-4029
7158656 CIFC17 H21 N3 O4P 21 21 217.1082; 14.5273; 31.578
90; 90; 90		3260.84Edmonds, Anthony K.; Oakes, Catherine S.; Hassell-Hart, Storm; Bruyère, Didier; Tizzard, Graham J.; Coles, Simon J.; Felix, Robert; Maple, Hannah J.; Marsh, Graham P.; Spencer, John
Scale-up and optimization of the synthesis of dual CBP/BRD4 inhibitor ISOX-DUAL.
Organic & biomolecular chemistry, 2022, 20, 4021-4029
7158657 CIFC17 H19 Cl N4 O3P c c n31.8053; 14.6164; 7.2574
90; 90; 90		3373.81Edmonds, Anthony K.; Oakes, Catherine S.; Hassell-Hart, Storm; Bruyère, Didier; Tizzard, Graham J.; Coles, Simon J.; Felix, Robert; Maple, Hannah J.; Marsh, Graham P.; Spencer, John
Scale-up and optimization of the synthesis of dual CBP/BRD4 inhibitor ISOX-DUAL.
Organic & biomolecular chemistry, 2022, 20, 4021-4029
7158658 CIFC26 H31 N3 O4P 1 21/c 113.0873; 12.461; 14.1989
90; 95.111; 90		2306.36Edmonds, Anthony K.; Oakes, Catherine S.; Hassell-Hart, Storm; Bruyère, Didier; Tizzard, Graham J.; Coles, Simon J.; Felix, Robert; Maple, Hannah J.; Marsh, Graham P.; Spencer, John
Scale-up and optimization of the synthesis of dual CBP/BRD4 inhibitor ISOX-DUAL.
Organic & biomolecular chemistry, 2022, 20, 4021-4029
7158659 CIFC17 H19 F N4 O3P 1 21/n 114.5932; 7.2583; 31.5918
90; 102.749; 90		3263.76Edmonds, Anthony K.; Oakes, Catherine S.; Hassell-Hart, Storm; Bruyère, Didier; Tizzard, Graham J.; Coles, Simon J.; Felix, Robert; Maple, Hannah J.; Marsh, Graham P.; Spencer, John
Scale-up and optimization of the synthesis of dual CBP/BRD4 inhibitor ISOX-DUAL.
Organic & biomolecular chemistry, 2022, 20, 4021-4029
7158661 CIFC22 H11 N5C 1 2/c 116.161; 11.81; 18.957
90; 100.689; 90		3555.4Huang, Shuangping; Ma, Jing; Yi, Yikun; Li, Mingtao; Cai, Ping; Wu, Na
Synthesis of orthogonal push-pull chromophores <i>via</i> click reaction of arylynamines.
Organic & biomolecular chemistry, 2022, 20, 4081-4085
7158662 CIFC34 H32 O10I 1 2/a 115.5676; 13.8531; 26.8877
90; 99.841; 90		5713.3Zhou, Tingting; Zheng, Anquan; Zhang, Wenge; Lu, Xiuxiang; Chen, Huiyu; Tan, Haibo
Concise total syntheses of two flavans and structure revision assisted by quantum NMR calculations.
Organic & biomolecular chemistry, 2022, 20, 4096-4100
7158663 CIFC13 H15 N O2P 1 21/c 19.581; 11.381; 10.941
90; 103.15; 90		1161.7Bhukta, Swadhapriya; Chatterjee, Rana; Dandela, Rambabu
Iodine-TBHP mediated efficient synthesis of α-ketoamides from vinyl azides and amines under mild conditions.
Organic & biomolecular chemistry, 2022, 20, 3907-3912
7158666 CIFC19 H14 N2 O SP -17.6918; 7.7847; 13.7184
90.026; 97.054; 114.557		740.27Meena, Neha; Dhiman, Shiv; Rangan, Krishnan; Kumar, Anil
Cobalt-catalyzed tandem one-pot synthesis of polysubstituted imidazo[1,5-<i>a</i>]pyridines and imidazo[1,5-<i>a</i>]isoquinolines.
Organic & biomolecular chemistry, 2022, 20, 4215-4223
7158669 CIFC16 H10 O5I 1 2/a 115.3058; 6.108; 28.2912
90; 101.503; 90		2591.76Si, Min; Yan, Jiaqi; Ding, Yongzheng; Huang, Hanmin
Pd-Catalyzed carbonylative lactonization of 2-halidearomatic aldehydes with H<sub>2</sub>O as a nucleophile.
Organic & biomolecular chemistry, 2022, 20, 3917-3921
7158670 CIFC16 H10 O5P 1 n 14.4392; 6.5027; 22.2547
90; 91.313; 90		642.25Si, Min; Yan, Jiaqi; Ding, Yongzheng; Huang, Hanmin
Pd-Catalyzed carbonylative lactonization of 2-halidearomatic aldehydes with H<sub>2</sub>O as a nucleophile.
Organic & biomolecular chemistry, 2022, 20, 3917-3921
7158678 CIFC29 H20 N O3 PP -110.5429; 10.9205; 11.7539
65.707; 75.725; 64.564		1109.9Peng, Lingteng; Hu, Zhifang; Zhao, Yanting; Peng, Lifen; Xu, Zhi; Yin, Shuang-Feng; Tang, Zilong; Qiu, Renhua; Kambe, Nobuaki
One-pot synthesis of phosphorylnaphth[2,1-<i>d</i>]oxazoles and products as P,N-ligands in C-N and C-C formation.
Organic & biomolecular chemistry, 2022, 20, 4110-4114
7158685 CIFC16 H19 N O5P -18.5101; 9.0807; 9.5903
77.657; 83.055; 88.402		718.67Ji, Kai-Long; Liu, Wei; Yin, Wei-Hang; Li, Jing-Ya; Yue, Jian-Min
Quinoline alkaloids with anti-inflammatory activity from <i>Zanthoxylum avicennae</i>.
Organic & biomolecular chemistry, 2022, 20, 4176-4182
7158686 CIFC15 H17 N O5P 1 21 19.7252; 7.2357; 10.0005
90; 98.737; 90		695.56Ji, Kai-Long; Liu, Wei; Yin, Wei-Hang; Li, Jing-Ya; Yue, Jian-Min
Quinoline alkaloids with anti-inflammatory activity from <i>Zanthoxylum avicennae</i>.
Organic & biomolecular chemistry, 2022, 20, 4176-4182
7158687 CIFC15 H17 N O4P 1 21 18.5948; 8.5216; 18.7212
90; 100.035; 90		1350.19Ji, Kai-Long; Liu, Wei; Yin, Wei-Hang; Li, Jing-Ya; Yue, Jian-Min
Quinoline alkaloids with anti-inflammatory activity from <i>Zanthoxylum avicennae</i>.
Organic & biomolecular chemistry, 2022, 20, 4176-4182
7158694 CIFC31 H34 N3 O4 SP -19.928; 11.674; 12.353
81.04; 82.19; 78.4		1377.2Mao, Biming; Xu, Jiaqing; Shi, Wangyu; Wang, Wei; Wu, Yongjun; Xiao, Yumei; Guo, Hongchao
Pd-Catalyzed [4 + 2] cycloaddition of methylene cyclic carbamates with dihydropyrazolone-derived alkenes: synthesis of spiropyrazolones.
Organic & biomolecular chemistry, 2022, 20, 4086-4090
7158695 CIFC62 H68 N6 O6 S2P -19.868; 11.707; 12.318
80.18; 82.46; 76.91		1359.4Mao, Biming; Xu, Jiaqing; Shi, Wangyu; Wang, Wei; Wu, Yongjun; Xiao, Yumei; Guo, Hongchao
Pd-Catalyzed [4 + 2] cycloaddition of methylene cyclic carbamates with dihydropyrazolone-derived alkenes: synthesis of spiropyrazolones.
Organic & biomolecular chemistry, 2022, 20, 4086-4090
7158697 CIFC27 H29 N O4P -19.0386; 10.9319; 13.2664
75.768; 71.588; 87.843		1204.42Singh, Prasoon Raj; Gopal, Braj; Kumar, Madan; Goswami, Avijit
A metal-free BF<sub>3</sub>·OEt<sub>2</sub> mediated chemoselective protocol for the synthesis of propargylic cyclic imines.
Organic & biomolecular chemistry, 2022, 20, 4933-4941
7158698 CIFC22 H14 N2 OP 1 21/c 13.8833; 16.3577; 23.692
90; 90.16; 90		1505Samanta, Surya Kanta; Sarkar, Rumpa; Sengupta, Utsav; Das, Sayan; Ganguly, Debabani; Hasija, Avantika; Chopra, Deepak; Bera, Mrinal K.
A direct entry to polycyclic quinoxaline derivatives <i>via</i> I<sub>2</sub>-DMSO mediated oxidative decarboxylation of α-amino acids and the subsequent Pictet-Spengler cyclization reaction.
Organic & biomolecular chemistry, 2022, 20, 4650-4658
7158699 CIFC21 H14 N2P 21 21 214.0812; 17.973; 19.807
90; 90; 90		1452.9Samanta, Surya Kanta; Sarkar, Rumpa; Sengupta, Utsav; Das, Sayan; Ganguly, Debabani; Hasija, Avantika; Chopra, Deepak; Bera, Mrinal K.
A direct entry to polycyclic quinoxaline derivatives <i>via</i> I<sub>2</sub>-DMSO mediated oxidative decarboxylation of α-amino acids and the subsequent Pictet-Spengler cyclization reaction.
Organic & biomolecular chemistry, 2022, 20, 4650-4658
7158702 CIFC25 H21 N O5P -111.8311; 12.9022; 14.4374
75.339; 70.665; 78.677		1996.47Hong, Kemiao; Yang, Xiangji; Zhang, Zhijing; Xie, Xiongda; Lv, Xin; Xu, Xinfang; Hu, Wenhao
Diastereoselective aldol-type interception of phenolic oxonium ylides for the direct assembly of 2,2-disubstituted dihydrobenzofurans.
Organic & biomolecular chemistry, 2022, 20, 4635-4639
7158710 CIFC3 H18 Hg2 I7 N9C 1 2/c 110.301; 11.919; 22.143
90; 100.5; 90		2673.1Yu, Chao; Yu, Yuyan; Sun, Longwu; Li, Xinzhi; Liu, Zhigang; Ke, Miaolin; Chen, Fener
Highly diastereo- and enantioselective synthesis of multisubstituted allylic amino acid derivatives by allylic alkylation of a chiral glycine-based nickel complex and vinylethylene carbonates.
Organic & biomolecular chemistry, 2022, 20, 4894-4899
7158711 CIFC37 H35 N3 Ni O4P 21 21 2110.3298; 13.1904; 22.5489
90; 90; 90		3072.38Yu, Chao; Yu, Yuyan; Sun, Longwu; Li, Xinzhi; Liu, Zhigang; Ke, Miaolin; Chen, Fener
Highly diastereo- and enantioselective synthesis of multisubstituted allylic amino acid derivatives by allylic alkylation of a chiral glycine-based nickel complex and vinylethylene carbonates.
Organic & biomolecular chemistry, 2022, 20, 4894-4899
7158713 CIFC37 H23 N3 O4P b c a17.4162; 11.9045; 34.111
90; 90; 90		7072.3Liu, Dan; Liu, Xueyan; Sun, Jing; Han, Ying; Yan, Chao-Guo
Domino reaction of bindone and 1,3-dipolarophiles for the synthesis of diverse spiro and fused indeno[1,2-<i>a</i>]fluorene-7,12-diones.
Organic & biomolecular chemistry, 2022, 20, 4964-4969
7158714 CIFC35 H20 O5P 1 21/n 18.5047; 27.831; 10.6483
90; 107.629; 90		2402Liu, Dan; Liu, Xueyan; Sun, Jing; Han, Ying; Yan, Chao-Guo
Domino reaction of bindone and 1,3-dipolarophiles for the synthesis of diverse spiro and fused indeno[1,2-<i>a</i>]fluorene-7,12-diones.
Organic & biomolecular chemistry, 2022, 20, 4964-4969
7158715 CIFC35 H20 O4P -17.992; 8.725; 17.432
87.327; 79.388; 89.684		1193.4Liu, Dan; Liu, Xueyan; Sun, Jing; Han, Ying; Yan, Chao-Guo
Domino reaction of bindone and 1,3-dipolarophiles for the synthesis of diverse spiro and fused indeno[1,2-<i>a</i>]fluorene-7,12-diones.
Organic & biomolecular chemistry, 2022, 20, 4964-4969
7158716 CIFC37 H24 O4P -18.297; 12.8462; 13.7948
114.993; 93.9003; 100.751		1291.33Liu, Dan; Liu, Xueyan; Sun, Jing; Han, Ying; Yan, Chao-Guo
Domino reaction of bindone and 1,3-dipolarophiles for the synthesis of diverse spiro and fused indeno[1,2-<i>a</i>]fluorene-7,12-diones.
Organic & biomolecular chemistry, 2022, 20, 4964-4969
7158717 CIFC38 H26 O4P 1 21/c 118.978; 12.483; 11.7028
90; 94.907; 90		2762.3Liu, Dan; Liu, Xueyan; Sun, Jing; Han, Ying; Yan, Chao-Guo
Domino reaction of bindone and 1,3-dipolarophiles for the synthesis of diverse spiro and fused indeno[1,2-<i>a</i>]fluorene-7,12-diones.
Organic & biomolecular chemistry, 2022, 20, 4964-4969
7158718 CIFC35 H22 N2 O3P 1 21/c 110.5877; 12.8107; 18.985
90; 91.436; 90		2574.2Liu, Dan; Liu, Xueyan; Sun, Jing; Han, Ying; Yan, Chao-Guo
Domino reaction of bindone and 1,3-dipolarophiles for the synthesis of diverse spiro and fused indeno[1,2-<i>a</i>]fluorene-7,12-diones.
Organic & biomolecular chemistry, 2022, 20, 4964-4969
7158719 CIFC38 H28 N2 O3P 1 21/c 19.7066; 12.5713; 23.8206
90; 100.881; 90		2854.4Liu, Dan; Liu, Xueyan; Sun, Jing; Han, Ying; Yan, Chao-Guo
Domino reaction of bindone and 1,3-dipolarophiles for the synthesis of diverse spiro and fused indeno[1,2-<i>a</i>]fluorene-7,12-diones.
Organic & biomolecular chemistry, 2022, 20, 4964-4969
7158720 CIFC42 H25 N O5P 1 21/c 112.9685; 13.8484; 20.7097
90; 93.367; 90		3712.9Liu, Dan; Liu, Xueyan; Sun, Jing; Han, Ying; Yan, Chao-Guo
Domino reaction of bindone and 1,3-dipolarophiles for the synthesis of diverse spiro and fused indeno[1,2-<i>a</i>]fluorene-7,12-diones.
Organic & biomolecular chemistry, 2022, 20, 4964-4969
7158721 CIFC43 H27 N O5P 1 21/c 113.3642; 14.9517; 20.5922
90; 90.279; 90		4114.6Liu, Dan; Liu, Xueyan; Sun, Jing; Han, Ying; Yan, Chao-Guo
Domino reaction of bindone and 1,3-dipolarophiles for the synthesis of diverse spiro and fused indeno[1,2-<i>a</i>]fluorene-7,12-diones.
Organic & biomolecular chemistry, 2022, 20, 4964-4969
7158730 CIFC23 H24 O7P 1 21/c 112.2709; 15.7729; 10.1394
90; 96.603; 90		1949.44Liu, Hongxin; Zhang, Yanjiang; Chen, Yuchan; Liu, Zhaoming; Tan, Haibo; Zhang, Weimin
Pyrone and isocoumarin derivatives from the endophytic fungus <i>Cytospora rhizophorae</i>.
Organic & biomolecular chemistry, 2022, 20, 4900-4904
7158745 CIFC59 H73 Dy N6 O5P 1 21/c 117.124; 14.155; 22.873
90; 106.7; 90		5310Chen, Zhichao; Zheng, Xinran; Zhou, Shu-Feng; Cui, Xiuling
Visible light-induced selenylative spirocyclization of biaryl ynones toward the formation of selenated spiro[5.5]trienones.
Organic & biomolecular chemistry, 2022, 20, 5779-5783
7158746 CIFC29 H22 O2 SeP -19.6751; 10.1384; 13.4857
107.731; 109.77; 93.109		1167.3Chen, Zhichao; Zheng, Xinran; Zhou, Shu-Feng; Cui, Xiuling
Visible light-induced selenylative spirocyclization of biaryl ynones toward the formation of selenated spiro[5.5]trienones.
Organic & biomolecular chemistry, 2022, 20, 5779-5783
7158747 CIFC16 H13 Br2 N OP -19.9894; 11.4609; 14.7673
106.052; 102.529; 106.772		1472.53Iwai, Kento; Mukaijo, Yusuke; Asahara, Haruyasu; Nishiwaki, Nagatoshi
A new approach to 10-arylated 5<i>H</i>-dibenzo[<i>b</i>,<i>f</i>]azepines using <i>syn</i>-selective hydrohalogenation of ethynylaniline.
Organic & biomolecular chemistry, 2022, 20, 5543-5550
7158748 CIFC23 H20 Br N OP 1 21/c 18.339; 10.6181; 21.0722
90; 92.485; 90		1864.07Iwai, Kento; Mukaijo, Yusuke; Asahara, Haruyasu; Nishiwaki, Nagatoshi
A new approach to 10-arylated 5<i>H</i>-dibenzo[<i>b</i>,<i>f</i>]azepines using <i>syn</i>-selective hydrohalogenation of ethynylaniline.
Organic & biomolecular chemistry, 2022, 20, 5543-5550
7158749 CIFC23 H19 N OP 1 21/c 115.5398; 8.6572; 13.0504
90; 99.779; 90		1730.18Iwai, Kento; Mukaijo, Yusuke; Asahara, Haruyasu; Nishiwaki, Nagatoshi
A new approach to 10-arylated 5<i>H</i>-dibenzo[<i>b</i>,<i>f</i>]azepines using <i>syn</i>-selective hydrohalogenation of ethynylaniline.
Organic & biomolecular chemistry, 2022, 20, 5543-5550
7158755 CIFC21 H30 N O4 PP -18.5489; 9.957; 12.8587
71.144; 81.512; 81.501		1018.59Kaźmierczak, Marcin; Dutkiewicz, Grzegorz; Koroniak, Henryk
Deoxyfluorinating reagents as tools for γ-amino-α-hydroxyphosphonate modification.
Organic & biomolecular chemistry, 2022, 20, 5615-5623
7158756 CIFC27 H34 N O4 PP -110.0312; 10.9576; 13.176
72.616; 81.716; 67.437		1275.6Kaźmierczak, Marcin; Dutkiewicz, Grzegorz; Koroniak, Henryk
Deoxyfluorinating reagents as tools for γ-amino-α-hydroxyphosphonate modification.
Organic & biomolecular chemistry, 2022, 20, 5615-5623
7158757 CIFC22 H32 N O4 PP -110.7214; 11.9743; 18.1464
88.453; 77.487; 74.219		2187.33Kaźmierczak, Marcin; Dutkiewicz, Grzegorz; Koroniak, Henryk
Deoxyfluorinating reagents as tools for γ-amino-α-hydroxyphosphonate modification.
Organic & biomolecular chemistry, 2022, 20, 5615-5623
7158758 CIFC15 H14 N2 O2P 1 21/c 111.1124; 11.301; 10.6161
90; 109.698; 90		1255.17Pawar, Amol Prakash; Yadav, Jyothi; Dolas, Atul Jankiram; Iype, Eldhose; Rangan, Krishnan; Kumar, Indresh
Catalyst-free direct regiospecific multicomponent synthesis of C3-functionalized pyrroles.
Organic & biomolecular chemistry, 2022, 20, 5747-5758
7158759 CIFC37 H35 N O2 PP -19.2756; 10.2061; 17.1546
79.024; 75.112; 74.328		1498.29Xu, Xin-Ming; Li, Wenzhong; Li, Qiwei; Chen, Sen; Zhang, Xuesi; Yang, Bin; Wang, Wei-Li
Manganese(III)-promoted highly stereoselective phosphorylation of acyclic tertiary enamides to synthesize <i>E</i>-selective β-phosphoryl enamides.
Organic & biomolecular chemistry, 2022, 20, 5566-5574
7158760 CIFC38 H39 Cl N4 O10 SP 1 21 110.2003; 9.935; 19.3125
90; 97.101; 90		1942.12Li, Tong-Hao; Niu, Cheng; Du, Da-Ming
Enantioselective synthesis of isoxazole-containing spirooxindole tetrahydroquinolines <i>via</i> squaramide-catalysed cascade reactions.
Organic & biomolecular chemistry, 2022, 20, 5582-5588
7158761 CIFC15 H13 N O2P 1 21/m 18.805; 6.864; 10.545
90; 110.673; 90		596.3Singh, Shashank; Tripathi, Krishna N.; Singh, Ravi P.
Redox activated amines in the organophotoinduced alkylation of coumarins.
Organic & biomolecular chemistry, 2022, 20, 5716-5720
7158762 CIFC19 H24 O4P -19.232; 9.6032; 10.3394
75.363; 80.372; 79.124		864.1Singh, Shashank; Tripathi, Krishna N.; Singh, Ravi P.
Redox activated amines in the organophotoinduced alkylation of coumarins.
Organic & biomolecular chemistry, 2022, 20, 5716-5720
7158765 CIFC11 H9 Br N2 O S2P -110.6549; 11.8312; 12.7053
62.656; 78.805; 65.198		1291.45Ravi Singh, Krishna; Santhosh, Chikkappaiahnayaka; Swaroop, Toreshettahally R.; Sadashiva, Maralinganadoddi P.
The regioselective synthesis of 2,5- and 4,5-disubstituted thiazoles <i>via</i> the cyclization of 2-oxo-2-(amino)ethanedithioates with isocyanides.
Organic & biomolecular chemistry, 2022, 20, 5771-5778
7158766 CIFC13 H11 Br N2 O3 SP 1 21/c 16.5681; 14.0924; 15.4674
90; 94.19; 90		1427.84Ravi Singh, Krishna; Santhosh, Chikkappaiahnayaka; Swaroop, Toreshettahally R.; Sadashiva, Maralinganadoddi P.
The regioselective synthesis of 2,5- and 4,5-disubstituted thiazoles <i>via</i> the cyclization of 2-oxo-2-(amino)ethanedithioates with isocyanides.
Organic & biomolecular chemistry, 2022, 20, 5771-5778

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