Crystallography Open Database

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7158089 CIFC11 H7 I N2P n a 2113.3693; 4.2733; 16.9207
90; 90; 90
966.7Liu, Yali; Wei, Yu; Yang, Zhen; Li, Yang; Liu, Yan; Liu, Ping
Highly selective C3-H iodination of pyrrolo[1,2-<i>a</i>]quinoxalines.
Organic & biomolecular chemistry, 2021, 19, 5191-5196
7158090 CIFC20 H17 Cl N4 O2P 1 21/c 114.3648; 14.4679; 8.6646
90; 101.1; 90
1767.1Zhuge, Juanping; Jiang, Ziyang; Jiang, Wei; Histand, Gary; Lin, Dongen
Iodine-catalyzed oxidative functionalization of purines with (thio)ethers or methylarenes for the synthesis of purin-8-one analogues.
Organic & biomolecular chemistry, 2021, 19, 5121-5126
7158091 CIFC116 H125 N13 O14P -116.27079; 24.574; 28.66463
112.948; 98.3767; 100.387
10081.8Pang, Zhi; Qi, Ting; Li, Baolin
Assembly and optical properties of 1D helical bundles induced by triphenylamine, side chains and solvents in crystals.
Organic & biomolecular chemistry, 2021, 19, 5555-5562
7158092 CIFC171.26 H177.04 N24 O31.26P -116.701; 20.4228; 24.065
89.126; 76.396; 87.174
7968.08Pang, Zhi; Qi, Ting; Li, Baolin
Assembly and optical properties of 1D helical bundles induced by triphenylamine, side chains and solvents in crystals.
Organic & biomolecular chemistry, 2021, 19, 5555-5562
7158093 CIFC104.58 H103.32 N13 O14.58P 1 21/n 110.3686; 31.9891; 31.1143
90; 95.405; 90
10274.2Pang, Zhi; Qi, Ting; Li, Baolin
Assembly and optical properties of 1D helical bundles induced by triphenylamine, side chains and solvents in crystals.
Organic & biomolecular chemistry, 2021, 19, 5555-5562
7158094 CIFC33 H28 Br N3 O2 SC 1 2/c 131.598; 11.6057; 21.0251
90; 129.356; 90
5961.7Chanda, Rupsa; Kar, Abhishek; Das, Aniruddha; Chakraborty, Baitan; Jana, Umasish
Iron-catalyzed carboarylation of alkynes <i>via</i> activation of π-activated alcohols: rapid synthesis of substituted benzofused six-membered heterocycles.
Organic & biomolecular chemistry, 2021, 19, 5155-5160
7158095 CIFC21 H24 N3 PP -19.4903; 9.865; 11.331
80.779; 71.403; 68.288
933Groutchik, Kristina; Jaiswal, Kuldeep; Dobrovetsky, Roman
An air-stable, Zn<sup>2+</sup>-based catalyst for hydrosilylation of alkenes and alkynes.
Organic & biomolecular chemistry, 2021, 19, 5544-5550
7158096 CIFC12 H18 B12 I12 N6 ZnR -3 m :H11.8876; 11.8876; 27.431
90; 90; 120
3357.1Groutchik, Kristina; Jaiswal, Kuldeep; Dobrovetsky, Roman
An air-stable, Zn<sup>2+</sup>-based catalyst for hydrosilylation of alkenes and alkynes.
Organic & biomolecular chemistry, 2021, 19, 5544-5550
7158097 CIFC21 H24 Cl2 N3 P ZnP 1 21/c 17.9597; 20.1364; 13.5168
90; 96.857; 90
2151Groutchik, Kristina; Jaiswal, Kuldeep; Dobrovetsky, Roman
An air-stable, Zn<sup>2+</sup>-based catalyst for hydrosilylation of alkenes and alkynes.
Organic & biomolecular chemistry, 2021, 19, 5544-5550
7158098 CIFC42 H48 B12 I12 N6 P2 ZnP 1 21/c 122.1697; 14.6015; 23.0686
90; 105.685; 90
7189.5Groutchik, Kristina; Jaiswal, Kuldeep; Dobrovetsky, Roman
An air-stable, Zn<sup>2+</sup>-based catalyst for hydrosilylation of alkenes and alkynes.
Organic & biomolecular chemistry, 2021, 19, 5544-5550
7158099 CIFC19 H18 Br N O2P 1 21/c 112.1783; 7.56305; 17.6627
90; 90.5451; 90
1626.75Zhao, Lan; Qiu, Changfu; Zhao, Lixin; Yin, Guangwei; Li, Fangyi; Wang, Chunhua; Li, Zheng
Base-promoted, CBr<sub>4</sub>-mediated tandem bromination/intramolecular Friedel-Crafts alkylation of N-aryl enamines: a facile access to 1H- and 3H-indoles.
Organic & biomolecular chemistry, 2021, 19, 5377-5382
7158100 CIFC12 H12.5 N O4P 1 21/n 112.5895; 5.0682; 18.033
90; 92.174; 90
1149.8Chen, Rongxiang; Jia, Ruo-Ling; Li, Wenbo; Zhao, Wei; Wang, Kai-Kai; Wang, Zhan-Yong; Ma, Xueji; Dai, Wei; Sun, Aili
A copper iodide-catalyzed coupling reaction of benzofuran-3(2H)-ones with amines: an approach to α-ketoamides.
Organic & biomolecular chemistry, 2021, 19, 5294-5297
7158102 CIFC34 H24 Cl4 N4 O4P 1 21/c 17.707; 17.6134; 22.5179
90; 93.088; 90
3052.29Kudale, Vishal Suresh; Mutra, Mohana Reddy; Chu, Ching-Piao; Wang, Jeh-Jeng
Unusual C<sub>3</sub>-acetylation of quinoxalin-2(1<i>H</i>)-one <i>via</i> oxidative C-C and C-O bond cleavages of PEG-400.
Organic & biomolecular chemistry, 2021, 19, 5567-5571
7158103 CIFC18 H16 N2 O2P 1 21/c 14.6921; 21.3139; 14.5759
90; 97.032; 90
1446.73Kudale, Vishal Suresh; Mutra, Mohana Reddy; Chu, Ching-Piao; Wang, Jeh-Jeng
Unusual C<sub>3</sub>-acetylation of quinoxalin-2(1<i>H</i>)-one <i>via</i> oxidative C-C and C-O bond cleavages of PEG-400.
Organic & biomolecular chemistry, 2021, 19, 5567-5571
7158104 CIFC42 H41 B F9 N3P -19.7145; 11.9901; 17.9234
103.282; 95.226; 109.005
1889.6Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Formation of amidino-borate derivatives by a multi-component reaction.
Organic & biomolecular chemistry, 2021, 19, 5551-5554
7158105 CIFC41 H39 B F9 N3P 21 21 2120.6283; 8.916; 19.7224
90; 90; 90
3627.38Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Formation of amidino-borate derivatives by a multi-component reaction.
Organic & biomolecular chemistry, 2021, 19, 5551-5554
7158106 CIFC56 H56 B F9 N3 PP 1 21/c 113.5769; 17.0284; 23.6162
90; 104.969; 90
5274.62Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Formation of amidino-borate derivatives by a multi-component reaction.
Organic & biomolecular chemistry, 2021, 19, 5551-5554
7158107 CIFC56 H56 B F9 N3 PP 1 21/c 113.3489; 16.9297; 23.6112
90; 101.316; 90
5232.2Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Formation of amidino-borate derivatives by a multi-component reaction.
Organic & biomolecular chemistry, 2021, 19, 5551-5554
7158108 CIFC32 H26 Br N O4.5I 1 2 17.179; 15.131; 26.209
90; 92.737; 90
2843.7Tsou, Yun-Jie; Guan, Ren-You; Han, Jeng-Liang
Enantioselective organocatalytic vinylogous aldol-cyclization cascade reaction of 3-alkylidene oxindoles with <i>o</i>-quinones.
Organic & biomolecular chemistry, 2021, 19, 5836-5843
7158109 CIFC28 H24 Br N O5P 21 21 217.217; 15.068; 23.762
90; 90; 90
2584Tsou, Yun-Jie; Guan, Ren-You; Han, Jeng-Liang
Enantioselective organocatalytic vinylogous aldol-cyclization cascade reaction of 3-alkylidene oxindoles with <i>o</i>-quinones.
Organic & biomolecular chemistry, 2021, 19, 5836-5843
7158110 CIFC22 H14 N2 OP 1 21/n 19.5943; 13.0289; 13.5767
90; 98.466; 90
1678.6Kim, Sunmi; Lee, Jeong Hwa; Yoon, Seok Hyun; Kim, Ikyon
A regioselective [4 + 2] annulation approach to 5-acylindolizine-7-carbonitriles: generation of poly-substituted pyridines.
Organic & biomolecular chemistry, 2021, 19, 5806-5817
7158111 CIFC13 H13 F3 N2 O3 SP b c a8.607; 14.6316; 22.5134
90; 90; 90
2835.2Panigrahi, Ahwan; Muniraj, Nachimuthu; Prabhu, Kandikere Ramaiah
<i>N</i>-Triflination of pyrazolones: a new method for N-S bond formation.
Organic & biomolecular chemistry, 2021, 19, 5534-5538
7158112 CIFC10 H16 F5 N O4 SA e a 213.4208; 26.557; 8.6349
90; 90; 90
3077.6DudziƄski, Piotr; Husstedt, Wibke S.; Matsnev, Andrej V.; Thrasher, Joseph S.; Haufe, Günter
Synthesis and [3,3]-sigmatropic rearrangements of 5-(pentafluorosulfanyl)-pent-3-en-2-ol, its homologues, and trifluoromethyl analogues.
Organic & biomolecular chemistry, 2021, 19, 5607-5623
7158113 CIFC19 H24 N2 O4P -19.9866; 10.417; 10.4938
101.921; 111.131; 105.454
924.18Zhang, Wei; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Li, Yinghua; Huang, Deguang
A three-component iodine-catalyzed oxidative coupling reaction: a heterodifunctionalization of 3-methylindoles.
Organic & biomolecular chemistry, 2021, 19, 5794-5799
7158114 CIFC17 H20 N2 O4P 1 21/n 18.7888; 19.6193; 10.0883
90; 109.798; 90
1636.71Zhang, Wei; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Li, Yinghua; Huang, Deguang
A three-component iodine-catalyzed oxidative coupling reaction: a heterodifunctionalization of 3-methylindoles.
Organic & biomolecular chemistry, 2021, 19, 5794-5799
7158115 CIFC18 H22 N2 O4P 1 21/n 19.0953; 19.6563; 10.0974
90; 109.55; 90
1701.14Zhang, Wei; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Li, Yinghua; Huang, Deguang
A three-component iodine-catalyzed oxidative coupling reaction: a heterodifunctionalization of 3-methylindoles.
Organic & biomolecular chemistry, 2021, 19, 5794-5799
7158116 CIFC68 H36 F4 O8 S8P 1 21/n 114.147; 5.4814; 18.975
90; 109.36; 90
1388.2Mondal, Santa; Yashmin, Sabina; Ali, Rashid; Soundaram, R.; Ghosh, Siddhartha S.; Khan, Abu Taleb
Synthesis of biologically active fused 1,4-oxathiin derivatives from 4-hydroxydithiocoumarins, arylacetylenes and dimethyl sulfoxide by Cu(i)-catalyzed C-H functionalization and cross-dehydrogenative C-S coupling reactions.
Organic & biomolecular chemistry, 2021, 19, 5818-5826
7158117 CIFC16 H21 N O4 SP 1 21 19.4481; 10.3898; 17.997
90; 96.944; 90
1753.7Li, Xue-Hong; Gong, Jun-Fang; Song, Mao-Ping
Diastereoselective synthesis of chiral 3-substituted isoindolinones <i>via</i> rhodium(III)-catalyzed oxidative C-H olefination/annulation.
Organic & biomolecular chemistry, 2021, 19, 5876-5887
7158118 CIFC15 H19 N O4 SP 21 21 218.6665; 9.0914; 20.0289
90; 90; 90
1578.09Li, Xue-Hong; Gong, Jun-Fang; Song, Mao-Ping
Diastereoselective synthesis of chiral 3-substituted isoindolinones <i>via</i> rhodium(III)-catalyzed oxidative C-H olefination/annulation.
Organic & biomolecular chemistry, 2021, 19, 5876-5887
7158119 CIFC8 H10 N2 O2P 1 21/c 15.9064; 18.7809; 7.4306
90; 97.589; 90
817.04Kasatkina, Svetlana O.; Geyl, Kirill K.; Baykov, Sergey V.; Boyarskaya, Irina A.; Boyarskiy, Vadim P.
Catalyst-free synthesis of substituted pyridin-2-yl, quinolin-2-yl, and isoquinolin-1-yl carbamates from the corresponding hetaryl ureas and alcohols.
Organic & biomolecular chemistry, 2021, 19, 6059-6065
7158120 CIFC9 H9 F3 N2 O2P -14.8119; 10.5336; 10.7314
114.87; 94.157; 90.003
491.92Kasatkina, Svetlana O.; Geyl, Kirill K.; Baykov, Sergey V.; Boyarskaya, Irina A.; Boyarskiy, Vadim P.
Catalyst-free synthesis of substituted pyridin-2-yl, quinolin-2-yl, and isoquinolin-1-yl carbamates from the corresponding hetaryl ureas and alcohols.
Organic & biomolecular chemistry, 2021, 19, 6059-6065
7158121 CIFC13 H14 N2 O3P 1 21/n 111.9095; 7.9623; 25.3411
90; 95.957; 90
2390.04Kasatkina, Svetlana O.; Geyl, Kirill K.; Baykov, Sergey V.; Boyarskaya, Irina A.; Boyarskiy, Vadim P.
Catalyst-free synthesis of substituted pyridin-2-yl, quinolin-2-yl, and isoquinolin-1-yl carbamates from the corresponding hetaryl ureas and alcohols.
Organic & biomolecular chemistry, 2021, 19, 6059-6065
7158122 CIFC13 H18 N2 O2P 1 21/n 18.3092; 12.0788; 11.8379
90; 92.429; 90
1187.05Kasatkina, Svetlana O.; Geyl, Kirill K.; Baykov, Sergey V.; Boyarskaya, Irina A.; Boyarskiy, Vadim P.
Catalyst-free synthesis of substituted pyridin-2-yl, quinolin-2-yl, and isoquinolin-1-yl carbamates from the corresponding hetaryl ureas and alcohols.
Organic & biomolecular chemistry, 2021, 19, 6059-6065
7158123 CIFC13 H14 N2 O3P -17.9429; 12.4375; 12.8747
87.653; 74.488; 87.068
1223.46Kasatkina, Svetlana O.; Geyl, Kirill K.; Baykov, Sergey V.; Boyarskaya, Irina A.; Boyarskiy, Vadim P.
Catalyst-free synthesis of substituted pyridin-2-yl, quinolin-2-yl, and isoquinolin-1-yl carbamates from the corresponding hetaryl ureas and alcohols.
Organic & biomolecular chemistry, 2021, 19, 6059-6065
7158124 CIFC16 H12 F N O2 SP -16.4301; 7.7504; 14.974
95.348; 100.866; 105.796
696.89Zhang, Zai-Wei; Rakesh, K. P.; Liu, Jing; Qin, Hua-Li; Tang, Haolin
A general approach to nitrile- and sulfonyl fluoride-substituted cyclopropanes.
Organic & biomolecular chemistry, 2021, 19, 6021-6024
7158125 CIFC10 H8 F N O2 SP 1 21/c 17.752; 23.836; 5.6189
90; 97.925; 90
1028.33Zhang, Zai-Wei; Rakesh, K. P.; Liu, Jing; Qin, Hua-Li; Tang, Haolin
A general approach to nitrile- and sulfonyl fluoride-substituted cyclopropanes.
Organic & biomolecular chemistry, 2021, 19, 6021-6024
7158126 CIFC13 H12 F N O4P 21 21 217.71; 9.8223; 16.1672
90; 90; 90
1224.34Banik, Swarnayu; Sahoo, Tanmoy; Sridhar, B.; Subba Reddy, B. V.
Enantioselective fluorination of 3-indolinone-2-carboxylates with NFSI catalyzed by chiral bisoxazolines.
Organic & biomolecular chemistry, 2021, 19, 6085-6091
7158130 CIFC17 H17 Cl2 N OP 3 1 c17.8125; 17.8125; 8.4655
90; 90; 120
2326.1Wang, Fang; Liu, Xiaoli; Wang, Lei
Visible-light-induced C(sp<sup>3</sup>)-H functionalizations of piperidines to 3,3-dichloro-2-hydroxy-piperidines with N-chlorosuccinimide.
Organic & biomolecular chemistry, 2021, 19, 6141-6146
7158131 CIFC18 H14 N2 O2P -17.2558; 9.8044; 10.5031
99.055; 105.174; 103.419
682.24Shelar, Santosh V.; Argade, Narshinha P.
Facile synthesis of indolizinoindolone, indolylepoxypyrrolooxazole, indolylpyrrolooxazolone and isoindolopyrazinoindolone heterocycles from indole and imide derivatives.
Organic & biomolecular chemistry, 2021, 19, 6160-6169
7158132 CIFC14 H14 N2 O2P c a 2124.406; 5.0265; 9.4136
90; 90; 90
1154.83Shelar, Santosh V.; Argade, Narshinha P.
Facile synthesis of indolizinoindolone, indolylepoxypyrrolooxazole, indolylpyrrolooxazolone and isoindolopyrazinoindolone heterocycles from indole and imide derivatives.
Organic & biomolecular chemistry, 2021, 19, 6160-6169
7158133 CIFC24 H35 Cl N8 O10P 21 21 216.7387; 9.5889; 44.6727
90; 90; 90
2886.6Morshed, Mahmud T.; Lacey, Ernest; Vuong, Daniel; Lacey, Alastair E.; Lean, Soo Sum; Moggach, Stephen A.; Karuso, Peter; Chooi, Yit-Heng; Booth, Thomas J.; Piggott, Andrew M.
Chlorinated metabolites from Streptomyces sp. highlight the role of biosynthetic mosaics and superclusters in the evolution of chemical diversity.
Organic & biomolecular chemistry, 2021, 19, 6147-6159
7158134 CIFC12 H14 O4P 1 21/c 115.6505; 4.3519; 17.2668
90; 115.015; 90
1065.72Wang, Lu; Huang, Yanbing; Zhang, Liping; Liu, Zhiwen; Liu, Wei; Xu, Huixin; Zhang, Qingbo; Zhang, Haibo; Yan, Yan; Liu, Zhiyong; Zhang, Tianyu; Zhang, Wenjun; Zhang, Changsheng
Structures and absolute configurations of phomalones from the coral-associated fungus Parengyodontium album sp. SCSIO 40430.
Organic & biomolecular chemistry, 2021, 19, 6030-6037
7158135 CIFC11.92 H13.91 O4P 1 21/c 15.1015; 21.7906; 10.1611
90; 102.619; 90
1102.27Wang, Lu; Huang, Yanbing; Zhang, Liping; Liu, Zhiwen; Liu, Wei; Xu, Huixin; Zhang, Qingbo; Zhang, Haibo; Yan, Yan; Liu, Zhiyong; Zhang, Tianyu; Zhang, Wenjun; Zhang, Changsheng
Structures and absolute configurations of phomalones from the coral-associated fungus Parengyodontium album sp. SCSIO 40430.
Organic & biomolecular chemistry, 2021, 19, 6030-6037
7158136 CIFC52 H76 O26P -110.3819; 12.0675; 12.3012
70.999; 84.623; 83.524
1445.2Wang, Lu; Huang, Yanbing; Zhang, Liping; Liu, Zhiwen; Liu, Wei; Xu, Huixin; Zhang, Qingbo; Zhang, Haibo; Yan, Yan; Liu, Zhiyong; Zhang, Tianyu; Zhang, Wenjun; Zhang, Changsheng
Structures and absolute configurations of phomalones from the coral-associated fungus Parengyodontium album sp. SCSIO 40430.
Organic & biomolecular chemistry, 2021, 19, 6030-6037
7158137 CIFC13 H14 O4P 1 21/c 112.1797; 5.2729; 17.2041
90; 99.215; 90
1090.63Wang, Lu; Huang, Yanbing; Zhang, Liping; Liu, Zhiwen; Liu, Wei; Xu, Huixin; Zhang, Qingbo; Zhang, Haibo; Yan, Yan; Liu, Zhiyong; Zhang, Tianyu; Zhang, Wenjun; Zhang, Changsheng
Structures and absolute configurations of phomalones from the coral-associated fungus Parengyodontium album sp. SCSIO 40430.
Organic & biomolecular chemistry, 2021, 19, 6030-6037
7158138 CIFC26 H38 O13C 1 2/c 123.3741; 13.2115; 17.727
90; 100.781; 90
5377.6Wang, Lu; Huang, Yanbing; Zhang, Liping; Liu, Zhiwen; Liu, Wei; Xu, Huixin; Zhang, Qingbo; Zhang, Haibo; Yan, Yan; Liu, Zhiyong; Zhang, Tianyu; Zhang, Wenjun; Zhang, Changsheng
Structures and absolute configurations of phomalones from the coral-associated fungus Parengyodontium album sp. SCSIO 40430.
Organic & biomolecular chemistry, 2021, 19, 6030-6037
7158139 CIFC34 H33 N3 O5P -110.0138; 11.7765; 12.7363
84.6324; 78.133; 84.1528
1458.14Zhan, Shao-Cong; Fang, Ren-Jie; Sun, Jing; Yan, Chao-Guo
Diastereoselective synthesis of spiro[carbazole-3,5'-pyrimidines] and spiro[carbazole-3,1'-cyclohexanes] <i>via</i> four-component reaction.
Organic & biomolecular chemistry, 2021, 19, 6322-6327
7158140 CIFC34 H33 N3 O5P 1 21/c 117.6658; 12.454; 26.766
90; 95.226; 90
5864.3Zhan, Shao-Cong; Fang, Ren-Jie; Sun, Jing; Yan, Chao-Guo
Diastereoselective synthesis of spiro[carbazole-3,5'-pyrimidines] and spiro[carbazole-3,1'-cyclohexanes] <i>via</i> four-component reaction.
Organic & biomolecular chemistry, 2021, 19, 6322-6327
7158141 CIFC34 H31 N3 O8P -110.8318; 11.4013; 15.4837
105.432; 103.175; 103.079
1708.8Zhan, Shao-Cong; Fang, Ren-Jie; Sun, Jing; Yan, Chao-Guo
Diastereoselective synthesis of spiro[carbazole-3,5'-pyrimidines] and spiro[carbazole-3,1'-cyclohexanes] <i>via</i> four-component reaction.
Organic & biomolecular chemistry, 2021, 19, 6322-6327
7158142 CIFC34 H27 Cl2 N O4P -110.7954; 11.0062; 13.5566
68.256; 87.382; 86.599
1493Zhan, Shao-Cong; Fang, Ren-Jie; Sun, Jing; Yan, Chao-Guo
Diastereoselective synthesis of spiro[carbazole-3,5'-pyrimidines] and spiro[carbazole-3,1'-cyclohexanes] <i>via</i> four-component reaction.
Organic & biomolecular chemistry, 2021, 19, 6322-6327
7158143 CIFC33 H30 Cl N3 O5P 1 21/n 18.6348; 17.8206; 18.8901
90; 94.7464; 90
2896.8Zhan, Shao-Cong; Fang, Ren-Jie; Sun, Jing; Yan, Chao-Guo
Diastereoselective synthesis of spiro[carbazole-3,5'-pyrimidines] and spiro[carbazole-3,1'-cyclohexanes] <i>via</i> four-component reaction.
Organic & biomolecular chemistry, 2021, 19, 6322-6327
7158144 CIFC34 H31 N3 O8P 1 21/n 113.3152; 11.0682; 20.681
90; 96.176; 90
3030.2Zhan, Shao-Cong; Fang, Ren-Jie; Sun, Jing; Yan, Chao-Guo
Diastereoselective synthesis of spiro[carbazole-3,5'-pyrimidines] and spiro[carbazole-3,1'-cyclohexanes] <i>via</i> four-component reaction.
Organic & biomolecular chemistry, 2021, 19, 6322-6327
7158145 CIFC33 H26 N4 O7P -18.9596; 9.371; 19.8144
99.221; 100.172; 96.4144
1599.44Zhan, Shao-Cong; Fang, Ren-Jie; Sun, Jing; Yan, Chao-Guo
Diastereoselective synthesis of spiro[carbazole-3,5'-pyrimidines] and spiro[carbazole-3,1'-cyclohexanes] <i>via</i> four-component reaction.
Organic & biomolecular chemistry, 2021, 19, 6322-6327
7158146 CIFC33 H30 N4 O7P -112.1728; 13.4083; 22.278
86.724; 89.748; 78.705
3559.8Zhan, Shao-Cong; Fang, Ren-Jie; Sun, Jing; Yan, Chao-Guo
Diastereoselective synthesis of spiro[carbazole-3,5'-pyrimidines] and spiro[carbazole-3,1'-cyclohexanes] <i>via</i> four-component reaction.
Organic & biomolecular chemistry, 2021, 19, 6322-6327
7158147 CIFC34 H33 N3 O7P 1 21/n 18.852; 18.3198; 18.4779
90; 95.474; 90
2982.8Zhan, Shao-Cong; Fang, Ren-Jie; Sun, Jing; Yan, Chao-Guo
Diastereoselective synthesis of spiro[carbazole-3,5'-pyrimidines] and spiro[carbazole-3,1'-cyclohexanes] <i>via</i> four-component reaction.
Organic & biomolecular chemistry, 2021, 19, 6322-6327
7158148 CIFC34 H33 N3 O6P 1 21/n 111.2751; 9.4901; 27.4393
90; 96.132; 90
2919.3Zhan, Shao-Cong; Fang, Ren-Jie; Sun, Jing; Yan, Chao-Guo
Diastereoselective synthesis of spiro[carbazole-3,5'-pyrimidines] and spiro[carbazole-3,1'-cyclohexanes] <i>via</i> four-component reaction.
Organic & biomolecular chemistry, 2021, 19, 6322-6327
7158149 CIFC28 H22 N6 S4C 1 2/c 116.8782; 17.0499; 19.0329
90; 99.6071; 90
5400.31An, Zhenyu; Wang, Ting; Liu, Yafeng; Ren, Yi; Yan, Rulong
A catalyst-free method for the synthesis of 1,4,2-dithiazoles from isothiocyanates and hydroxylamine triflic acid salts.
Organic & biomolecular chemistry, 2021, 19, 6206-6209
7158150 CIFC25 H23 N O3 S2P -19.009; 9.253; 13.987
106.407; 94.581; 91.51
1113.4Xie, Jianwei; Suleman, Muhammad; Wang, Zaibin; Mao, Xinfei; Mao, Beibei; Fan, Jiale; Lu, Ping; Wang, Yanguang
Syntheses of 4-allyl-/4-allenyl-4-(arylthio)-1,4-dihydroisoquinolin-3-ones <i>via</i> the photochemical Doyle-Kirmse reaction.
Organic & biomolecular chemistry, 2021, 19, 6341-6345
7158151 CIFC14 H11 N O7 SP 1 21/c 110.61747; 13.02984; 10.52228
90; 101.882; 90
1424.5Hawkins, Paige M. E.; Liu, Dennis Y.; Linington, Roger G.; Payne, Richard J.
Solid-phase synthesis of coralmycin A/<i>epi</i>-coralmycin A and desmethoxycoralmycin A.
Organic & biomolecular chemistry, 2021, 19, 6291-6300
7158152 CIFC14 H22 O2 S Si2C 1 2/c 122.436; 6.47; 23.601
90; 98.711; 90
3386Nobuhara, Keita; Inagaki, Yusuke; Setaka, Wataru
Steric effects on the intramolecular charge transfer fluorescence of benzo[<i>b</i>]thiophene-1,1-dioxide bridged macrocages.
Organic & biomolecular chemistry, 2021, 19, 6328-6333
7158153 CIFC11 H9 N3P c c n14.159; 17.002; 7.473
90; 90; 90
1799Zhang, Xiaomin; Yang, Jiali; Xiong, Ni; Han, Zhe; Duan, Xinhua; Zeng, Rong
Indium-mediated annulation of 2-azidoaryl aldehydes with propargyl bromides to [1,2,3]triazolo[1,5-<i>a</i>]quinolines.
Organic & biomolecular chemistry, 2021, 19, 6346-6352
7158154 CIFC20 H26 O4 S SiP 1 21/n 111.9277; 10.9677; 15.6981
90; 97.067; 90
2038.02Zhang, Ye; Guo, Jingcheng; Han, Jinna; Zhou, Xiangui; Cao, Wei; Fu, Zhenqian
Bifunctional squaramide catalyzed asymmetric synthesis of chiral α-mercaptosilanes.
Organic & biomolecular chemistry, 2021, 19, 6412-6416
7158155 CIFC24 H21 N3 O3P b c a12.1633; 16.9191; 20.785
90; 90; 90
4277.4Li, Wenhui; Xin, Jie; Zhai, Pingan; Lin, Jianying; Huang, Shuangping; Gao, Wenchao; Li, Xing
Access to highly functionalized imidazolones bearing α-amino acid esters <i>via</i> KOH-promoted annulation of amidines, nitrosoarenes and malonic esters.
Organic & biomolecular chemistry, 2021, 19, 6473-6477
7158156 CIFC26 H22 Cl N OP 1 21/c 17.5536; 15.5289; 19.9941
90; 98.847; 90
2317.39Clarke, Joshua J.; Devaraj, Karthik; Bestvater, Brian P.; Kojima, Ryoto; Eisenberger, Patrick; DeJesus, Joseph F.; Crudden, Cathleen M.
Hydrosilylation and Mukaiyama aldol-type reaction of quinolines and hydrosilylation of imines catalyzed by a mesoionic carbene-stabilized borenium ion.
Organic & biomolecular chemistry, 2021, 19, 6786-6791
7158157 CIFC26 H21 N3 O SP 1 21 18.6611; 13.0943; 10.2975
90; 110.729; 90
1092.25Vroemans, Robby; Ribone, Sergio R.; Thomas, Joice; Van Meervelt, Luc; Ollevier, Thierry; Dehaen, Wim
Synthesis of homochiral sulfanyl- and sulfoxide-substituted naphthyltriazoles and study of the conformational stability.
Organic & biomolecular chemistry, 2021, 19, 6521-6526
7158158 CIFC26 H21 N3 O2 SP 21 21 216.8461; 15.7021; 21.1251
90; 90; 90
2270.91Vroemans, Robby; Ribone, Sergio R.; Thomas, Joice; Van Meervelt, Luc; Ollevier, Thierry; Dehaen, Wim
Synthesis of homochiral sulfanyl- and sulfoxide-substituted naphthyltriazoles and study of the conformational stability.
Organic & biomolecular chemistry, 2021, 19, 6521-6526
7158159 CIFC26 H21 N3 O2 SP 21 21 2121.3972; 14.6607; 6.86195
90; 90; 90
2152.58Vroemans, Robby; Ribone, Sergio R.; Thomas, Joice; Van Meervelt, Luc; Ollevier, Thierry; Dehaen, Wim
Synthesis of homochiral sulfanyl- and sulfoxide-substituted naphthyltriazoles and study of the conformational stability.
Organic & biomolecular chemistry, 2021, 19, 6521-6526
7158160 CIFC26 H21 N3 O2 SP 21 21 218.2288; 10.1233; 25.6942
90; 90; 90
2140.4Vroemans, Robby; Ribone, Sergio R.; Thomas, Joice; Van Meervelt, Luc; Ollevier, Thierry; Dehaen, Wim
Synthesis of homochiral sulfanyl- and sulfoxide-substituted naphthyltriazoles and study of the conformational stability.
Organic & biomolecular chemistry, 2021, 19, 6521-6526
7158161 CIFC19 H30 N4 O12P -18.694; 18.217; 34.494
89.931; 89.94; 89.969
5463Kulkarni, Pradnya; Datta, Dhrubajyoti; Ramabhadran, Raghunath O.; Ganesh, Krishna
Gem-dimethyl peptide nucleic acid (α/β/γ-<i>gdm</i>-PNA) monomers: synthesis and the role of <i>gdm</i>-substituents in preferential stabilisation of <i>Z</i>/<i>E</i>-rotamers.
Organic & biomolecular chemistry, 2021, 19, 6534-6545
7158162 CIFC17 H19 N5 O2 S2P 1 21 19.0334; 8.7125; 12.1508
90; 94.034; 90
953.94Shi, Di; Cao, Jinlian; Weng, Peimin; Yan, Xiaosheng; Li, Zhao; Jiang, Yun-Bao
Chalcogen bonding mediates the formation of supramolecular helices of azapeptides in crystals.
Organic & biomolecular chemistry, 2021, 19, 6397-6401
7158163 CIFC15 H16 N4 O2 S2P 1 21 110.1096; 8.1557; 10.7216
90; 110.545; 90
827.78Shi, Di; Cao, Jinlian; Weng, Peimin; Yan, Xiaosheng; Li, Zhao; Jiang, Yun-Bao
Chalcogen bonding mediates the formation of supramolecular helices of azapeptides in crystals.
Organic & biomolecular chemistry, 2021, 19, 6397-6401
7158164 CIFC20 H22 Br N O5P 1 21 112.3447; 5.563; 17.4342
90; 104.256; 90
1160.4Fang, Guosheng; Wang, Hongyu; Zheng, Changwu; Pan, Lu; Zhao, Gang
Enantioselectivity switch in asymmetric Michael addition reactions using phosphonium salts.
Organic & biomolecular chemistry, 2021, 19, 6334-6340
7158165 CIFC39 H32 Br F12 N2 O2 PP 18.7747; 15.1721; 16.458
72.036; 88.944; 84.345
2073.94Fang, Guosheng; Wang, Hongyu; Zheng, Changwu; Pan, Lu; Zhao, Gang
Enantioselectivity switch in asymmetric Michael addition reactions using phosphonium salts.
Organic & biomolecular chemistry, 2021, 19, 6334-6340
7158166 CIFC8 H4 F3 I N2 O3P 1 21/c 14.9637; 20.0442; 10.3335
90; 101.298; 90
1008.19Kobayashi, Yusuke; Masakado, Sota; Murai, Takuya; Hamada, Shohei; Furuta, Takumi; Takemoto, Yoshiji
A bench-stable N-trifluoroacetyl nitrene equivalent for a simple synthesis of 2-trifluoromethyl oxazoles.
Organic & biomolecular chemistry, 2021, 19, 6628-6632
7158167 CIFC16 H12 O3P -17.0451; 7.3918; 12.782
76.201; 81.124; 73.395
616.8Wu, Hao; Wang, Yi-Chun; Shatskiy, Andrey; Li, Qiu-Yan; Liu, Jian-Quan; Kärkäs, Markus D; Wang, Xiang-Shan
Modular synthesis of 3-substituted isocoumarins <i>via</i> silver-catalyzed aerobic oxidation/<i>6-endo</i> heterocyclization of <i>ortho</i>-alkynylbenzaldehydes.
Organic & biomolecular chemistry, 2021, 19, 6657-6664
7158168 CIFC16 H12 N2 O2P b c a15.006; 6.157; 27.288
90; 90; 90
2521.2Lai, Huifang; Xu, Jiexin; Lin, Jin; Zha, Daijun
Copper-promoted direct amidation of isoindolinone scaffolds by sodium persulfate.
Organic & biomolecular chemistry, 2021, 19, 7621-7626
7158169 CIFC12 H12 N2 O2P 1 21/n 19.806; 11.637; 9.954
90; 105.446; 90
1094.8Lai, Huifang; Xu, Jiexin; Lin, Jin; Zha, Daijun
Copper-promoted direct amidation of isoindolinone scaffolds by sodium persulfate.
Organic & biomolecular chemistry, 2021, 19, 7621-7626
7158170 CIFC40 H33 Br N4 OP -112.2987; 12.4224; 13.2018
75.801; 69.663; 66.425
1720.08Nawaz, Shah; Wei, Shiqiang; Huang, Yue; Wang, Wenyao; Qu, Jingping; Wang, Baomin
Diastereoselective synthesis of indolenine-based spiro[pyrazolone-4,2'-pyrrolidine] scaffolds via 1,3-dipolar cycloaddition of 4-aminopyrazolones, aldehydes, and indolenines.
Organic & biomolecular chemistry, 2021, 19, 6964-6968
7158171 CIFC39 H32 O3 P2P -110.8036; 11.4967; 15.6103
95.672; 91.026; 113.558
1765.1Fan, Tao; Liu, Yan; Jiang, Caina; Xu, Yanli; Chen, Yanyan
A metal-free radical cascade reaction of phosphine oxides with 2-aryloxy phenylacetylenes to synthesize diphosphonyl xanthene derivatives.
Organic & biomolecular chemistry, 2021, 19, 6609-6612
7158172 CIFC19 H15 F I N O4 SP 1 21/n 18.4116; 18.7873; 12.526
90; 98.829; 90
1956.04Habert, Loïc; Diachenko, Iryna; Retailleau, Pascal; Gillaizeau, Isabelle
Electrophile promoted cyclization of <i>ortho</i>-aryl substituted ynamides: construction of 3-amino-4-halo- or 4 seleno-isocoumarin derivatives.
Organic & biomolecular chemistry, 2021, 19, 6623-6627
7158173 CIFC14 H9 Cl N2 OP 1 21/c 15.1089; 22.0087; 10.5605
90; 99.571; 90
1170.9Abeysekera, Amila M.; Averkiev, Boris B.; Le Magueres, Pierre; Aakeröy, Christer B
Intermolecular binding preferences of haloethynyl halogen-bond donors as a function of molecular electrostatic potentials in a family of <i>N</i>-(pyridin-2-yl)amides.
Organic & biomolecular chemistry, 2021, 19, 6671-6681
7158174 CIFC13 H8 Br N3 OP 1 21/n 13.8797; 21.319; 14.8922
90; 95.148; 90
1226.78Abeysekera, Amila M.; Averkiev, Boris B.; Le Magueres, Pierre; Aakeröy, Christer B
Intermolecular binding preferences of haloethynyl halogen-bond donors as a function of molecular electrostatic potentials in a family of <i>N</i>-(pyridin-2-yl)amides.
Organic & biomolecular chemistry, 2021, 19, 6671-6681
7158175 CIFC13 H8 I N3 OC 1 2/c 110.21; 13.0373; 18.718
90; 103.054; 90
2427.18Abeysekera, Amila M.; Averkiev, Boris B.; Le Magueres, Pierre; Aakeröy, Christer B
Intermolecular binding preferences of haloethynyl halogen-bond donors as a function of molecular electrostatic potentials in a family of <i>N</i>-(pyridin-2-yl)amides.
Organic & biomolecular chemistry, 2021, 19, 6671-6681
7158176 CIFC13 H8 Cl N3 OP 1 21/c 13.7735; 10.1396; 29.0994
90; 90.876; 90
1113.26Abeysekera, Amila M.; Averkiev, Boris B.; Le Magueres, Pierre; Aakeröy, Christer B
Intermolecular binding preferences of haloethynyl halogen-bond donors as a function of molecular electrostatic potentials in a family of <i>N</i>-(pyridin-2-yl)amides.
Organic & biomolecular chemistry, 2021, 19, 6671-6681
7158177 CIFC13 H8 I N3 OP 1 21/c 112.7284; 6.7266; 14.4741
90; 104.558; 90
1199.47Abeysekera, Amila M.; Averkiev, Boris B.; Le Magueres, Pierre; Aakeröy, Christer B
Intermolecular binding preferences of haloethynyl halogen-bond donors as a function of molecular electrostatic potentials in a family of <i>N</i>-(pyridin-2-yl)amides.
Organic & biomolecular chemistry, 2021, 19, 6671-6681
7158178 CIFC13 H8 Cl N3 OP 1 21/c 13.846; 9.8013; 29.8606
90; 93.485; 90
1123.54Abeysekera, Amila M.; Averkiev, Boris B.; Le Magueres, Pierre; Aakeröy, Christer B
Intermolecular binding preferences of haloethynyl halogen-bond donors as a function of molecular electrostatic potentials in a family of <i>N</i>-(pyridin-2-yl)amides.
Organic & biomolecular chemistry, 2021, 19, 6671-6681
7158179 CIFC13 H8 Cl N3 OP 1 21/c 13.7981; 11.5441; 25.4972
90; 91.106; 90
1117.73Abeysekera, Amila M.; Averkiev, Boris B.; Le Magueres, Pierre; Aakeröy, Christer B
Intermolecular binding preferences of haloethynyl halogen-bond donors as a function of molecular electrostatic potentials in a family of <i>N</i>-(pyridin-2-yl)amides.
Organic & biomolecular chemistry, 2021, 19, 6671-6681
7158180 CIFC14 H9 I N2 OP 1 21/c 14.0845; 16.1979; 19.1245
90; 95.784; 90
1258.84Abeysekera, Amila M.; Averkiev, Boris B.; Le Magueres, Pierre; Aakeröy, Christer B
Intermolecular binding preferences of haloethynyl halogen-bond donors as a function of molecular electrostatic potentials in a family of <i>N</i>-(pyridin-2-yl)amides.
Organic & biomolecular chemistry, 2021, 19, 6671-6681
7158181 CIFC14 H9 I N2 OP 1 21/n 15.2552; 15.3923; 16.4781
90; 98.244; 90
1319.13Abeysekera, Amila M.; Averkiev, Boris B.; Le Magueres, Pierre; Aakeröy, Christer B
Intermolecular binding preferences of haloethynyl halogen-bond donors as a function of molecular electrostatic potentials in a family of <i>N</i>-(pyridin-2-yl)amides.
Organic & biomolecular chemistry, 2021, 19, 6671-6681
7158182 CIFC14 H9 Br N2 OP 1 21/c 15.1974; 21.9187; 10.6585
90; 100.577; 90
1193.59Abeysekera, Amila M.; Averkiev, Boris B.; Le Magueres, Pierre; Aakeröy, Christer B
Intermolecular binding preferences of haloethynyl halogen-bond donors as a function of molecular electrostatic potentials in a family of <i>N</i>-(pyridin-2-yl)amides.
Organic & biomolecular chemistry, 2021, 19, 6671-6681
7158183 CIFC13 H8 Br N3 OP -16.7509; 9.2249; 10.2422
112.512; 93.859; 97.72
578.97Abeysekera, Amila M.; Averkiev, Boris B.; Le Magueres, Pierre; Aakeröy, Christer B
Intermolecular binding preferences of haloethynyl halogen-bond donors as a function of molecular electrostatic potentials in a family of <i>N</i>-(pyridin-2-yl)amides.
Organic & biomolecular chemistry, 2021, 19, 6671-6681
7158184 CIFC20 H11 F N4P 1 21/c 111.4106; 14.3958; 9.9664
90; 94.167; 90
1632.8Chakraborty, Nikita; Dahiya, Anjali; Rakshit, Amitava; Modi, Anju; Patel, Bhisma K.
An expedient route to tricyanovinylindoles and indolylmaleimides from o-alkynylanilines utilising DMSO as a one-carbon synthon.
Organic & biomolecular chemistry, 2021, 19, 6847-6857
7158185 CIFC18 H25 N2 O4 PP 1 21/n 114.4732; 8.9061; 15.9214
90; 109.314; 90
1936.76Tajti, Ádám; Szabó, Kármen EmƑke; Popovics-Tóth, Nóra; Iskanderov, Javad; Perdih, Franc; Hackler, László; Kari, Beáta; Puskás, László G; Bálint, Erika
PMDTA-catalyzed multicomponent synthesis and biological activity of 2-amino-4H-chromenes containing a phosphonate or phosphine oxide moiety.
Organic & biomolecular chemistry, 2021, 19, 6883-6891
7158186 CIFC24 H20 N3 O2 PP 1 21/c 112.3634; 10.7573; 15.9936
90; 101.939; 90
2081.1Tajti, Ádám; Szabó, Kármen EmƑke; Popovics-Tóth, Nóra; Iskanderov, Javad; Perdih, Franc; Hackler, László; Kari, Beáta; Puskás, László G; Bálint, Erika
PMDTA-catalyzed multicomponent synthesis and biological activity of 2-amino-4H-chromenes containing a phosphonate or phosphine oxide moiety.
Organic & biomolecular chemistry, 2021, 19, 6883-6891
7158187 CIFC26 H25 N2 O5 PP -19.9066; 9.9454; 12.3415
102.791; 101.823; 90.163
1159.14Tajti, Ádám; Szabó, Kármen EmƑke; Popovics-Tóth, Nóra; Iskanderov, Javad; Perdih, Franc; Hackler, László; Kari, Beáta; Puskás, László G; Bálint, Erika
PMDTA-catalyzed multicomponent synthesis and biological activity of 2-amino-4H-chromenes containing a phosphonate or phosphine oxide moiety.
Organic & biomolecular chemistry, 2021, 19, 6883-6891
7158188 CIFC26 H25 N2 O2 PP 1 21/c 112.9952; 11.0767; 15.1578
90; 93.224; 90
2178.42Tajti, Ádám; Szabó, Kármen EmƑke; Popovics-Tóth, Nóra; Iskanderov, Javad; Perdih, Franc; Hackler, László; Kari, Beáta; Puskás, László G; Bálint, Erika
PMDTA-catalyzed multicomponent synthesis and biological activity of 2-amino-4H-chromenes containing a phosphonate or phosphine oxide moiety.
Organic & biomolecular chemistry, 2021, 19, 6883-6891
7158189 CIFC24 H21 N2 O2 PP -19; 11.1653; 12.3858
115.027; 91.058; 113.01
1012.5Tajti, Ádám; Szabó, Kármen EmƑke; Popovics-Tóth, Nóra; Iskanderov, Javad; Perdih, Franc; Hackler, László; Kari, Beáta; Puskás, László G; Bálint, Erika
PMDTA-catalyzed multicomponent synthesis and biological activity of 2-amino-4H-chromenes containing a phosphonate or phosphine oxide moiety.
Organic & biomolecular chemistry, 2021, 19, 6883-6891
7158190 CIFC30 H25 O5 PP 1 21/c 19.32193; 15.92387; 17.03098
90; 91.9636; 90
2526.61Zheng, Shi-Lu; Zou, Yun-Xiang; Wen, Zhong; Lin, Jia-Fu; Gu, Ling-Hui; Chen, Long
Y(OTf)<sub>3</sub>-catalyzed phosphorylation of 2H-chromene hemiacetals with P(O)-H compounds to 2-phosphorylated 2H-chromenes.
Organic & biomolecular chemistry, 2021, 19, 6812-6816
7158191 CIFC32 H29 N O6 SP 1 21/n 110.7889; 23.8675; 11.6684
90; 113.658; 90
2752.14Lodhi, Rajni; Prakash, Meher; Samanta, Sampak
Diastereoselective desymmetrization reactions of prochiral para-quinamines with cyclopropenes generated in situ: access to fused hydroindol-5-one scaffolds.
Organic & biomolecular chemistry, 2021, 19, 7129-7133
7158192 CIFC17 H14 Cl N O4P 1 21/c 111.168; 15.73; 18.35
90; 105.575; 90
3105.2Ge, Yuhua; Chen, Xingyue; Dong, Yi; Wang, Hua-Nan; Li, Yangyan; Chen, Gang
Access to benzene-modified 2<sup>nd</sup> generation strigolactams and GR24 by merging C-H olefination with decarboxylative Giese cyclization.
Organic & biomolecular chemistry, 2021, 19, 7141-7146
7158193 CIFC17 H13 Cl O5P 1 21/n 112.588; 7.415; 16.351
90; 100.998; 90
1498.2Ge, Yuhua; Chen, Xingyue; Dong, Yi; Wang, Hua-Nan; Li, Yangyan; Chen, Gang
Access to benzene-modified 2<sup>nd</sup> generation strigolactams and GR24 by merging C-H olefination with decarboxylative Giese cyclization.
Organic & biomolecular chemistry, 2021, 19, 7141-7146
7158194 CIFC1.55 H1.45 O0.45P n a 219.97; 11.919; 12.5827
90; 90; 90
1495.23Chen, Yan-Shan; Zheng, Yu; Chen, Zhi-Jun; Xie, Zhen-Zhen; He, Xian-Chen; Xiao, Jun-An; Chen, Kai; Xiang, Hao-Yue; Yang, Hua
A phosphine-catalysed one-pot domino sequence to access cyclopentene-fused coumarins.
Organic & biomolecular chemistry, 2021, 19, 7074-7080
7158195 CIFC32 H28 O8P -110.2334; 12.1426; 12.2272
115.446; 93.73; 103.262
1312Chen, Yan-Shan; Zheng, Yu; Chen, Zhi-Jun; Xie, Zhen-Zhen; He, Xian-Chen; Xiao, Jun-An; Chen, Kai; Xiang, Hao-Yue; Yang, Hua
A phosphine-catalysed one-pot domino sequence to access cyclopentene-fused coumarins.
Organic & biomolecular chemistry, 2021, 19, 7074-7080
7158196 CIFC21 H16 N2 O3P 1 21/n 18.9293; 10.0916; 18.8422
90; 96.1923; 90
1687.98Chen, Yan-Shan; Zheng, Yu; Chen, Zhi-Jun; Xie, Zhen-Zhen; He, Xian-Chen; Xiao, Jun-An; Chen, Kai; Xiang, Hao-Yue; Yang, Hua
A phosphine-catalysed one-pot domino sequence to access cyclopentene-fused coumarins.
Organic & biomolecular chemistry, 2021, 19, 7074-7080
7158197 CIFC38 H33 Cl2 I2 O P2 RhP -110.1542; 13.7673; 14.3456
72.6361; 88.2388; 74.6748
1843.48Okada, Masaki; Takeuchi, Katsuhiko; Matsumoto, Kazuhiro; Oku, Tomoharu; Choi, Jun-Chul
Hydroxycarbonylation of alkenes with formic acid using a rhodium iodide complex and alkyl ammonium iodide.
Organic & biomolecular chemistry, 2021, 19, 8727-8734
7158198 CIFC25 H25 N O3P -18.6227; 11.3588; 11.8411
117.309; 91.977; 96.236
1019.7Ding, Weiwei; Zhang, Gang
Access to fused π-extended acridone derivatives through a regioselective oxidative demethylation.
Organic & biomolecular chemistry, 2021, 19, 6985-6989
7158199 CIFC32 H27 Cl6 N3 O2P 1 21/c 111.7193; 25.313; 11.1041
90; 105.097; 90
3180.3Ding, Weiwei; Zhang, Gang
Access to fused π-extended acridone derivatives through a regioselective oxidative demethylation.
Organic & biomolecular chemistry, 2021, 19, 6985-6989
7158200 CIFC36 H29 Cl6 N3 O2P -111.5804; 12.1813; 12.9925
101.203; 101.376; 103.039
1694.85Ding, Weiwei; Zhang, Gang
Access to fused π-extended acridone derivatives through a regioselective oxidative demethylation.
Organic & biomolecular chemistry, 2021, 19, 6985-6989
7158201 CIFC22 H19 N O2 SP 1 21/n 111.613; 10.494; 15.562
90; 91.952; 90
1895.4Sandeep, K.; Siva Reddy, Alla; Kumara Swamy, K. C.
Palladium-catalysed cyclisation of ynamides and propargyl tethered iodosulfonamides with boronic acids leading to benzosultams.
Organic & biomolecular chemistry, 2021, 19, 6871-6882
7158202 CIFC21 H19 N O2 S2P -19.8974; 9.9589; 11.7524
90.477; 106.658; 116.051
984.84Sandeep, K.; Siva Reddy, Alla; Kumara Swamy, K. C.
Palladium-catalysed cyclisation of ynamides and propargyl tethered iodosulfonamides with boronic acids leading to benzosultams.
Organic & biomolecular chemistry, 2021, 19, 6871-6882
7158203 CIFC22 H18 Cl N O2 SP -110.0494; 10.1081; 10.9713
104.997; 112.432; 95.785
969.89Sandeep, K.; Siva Reddy, Alla; Kumara Swamy, K. C.
Palladium-catalysed cyclisation of ynamides and propargyl tethered iodosulfonamides with boronic acids leading to benzosultams.
Organic & biomolecular chemistry, 2021, 19, 6871-6882
7158204 CIFC20 H21 N O2 SP 1 21/c 120.5737; 6.0343; 14.7085
90; 104.444; 90
1768.31Sandeep, K.; Siva Reddy, Alla; Kumara Swamy, K. C.
Palladium-catalysed cyclisation of ynamides and propargyl tethered iodosulfonamides with boronic acids leading to benzosultams.
Organic & biomolecular chemistry, 2021, 19, 6871-6882
7158205 CIFC46 H42 N2 O4 S2P -19.9875; 14.1732; 14.8341
83.86; 80.349; 74.882
1994.06Sandeep, K.; Siva Reddy, Alla; Kumara Swamy, K. C.
Palladium-catalysed cyclisation of ynamides and propargyl tethered iodosulfonamides with boronic acids leading to benzosultams.
Organic & biomolecular chemistry, 2021, 19, 6871-6882
7158206 CIFC12 H14 I2 N2P n m a12.7742; 7.1824; 15.7199
90; 90; 90
1442.29Sysoeva, Alexandra A.; Novikov, Alexander S.; Il'in, Mikhail V.; Suslonov, Vitalii V.; Bolotin, Dmitrii S.
Predicting the catalytic activity of azolium-based halogen bond donors: an experimentally-verified theoretical study.
Organic & biomolecular chemistry, 2021, 19, 7611-7620
7158207 CIFC13 H14 F3 I N2 O3 SP 1 21/c 18.3762; 14.1584; 14.0266
90; 97.152; 90
1650.52Sysoeva, Alexandra A.; Novikov, Alexander S.; Il'in, Mikhail V.; Suslonov, Vitalii V.; Bolotin, Dmitrii S.
Predicting the catalytic activity of azolium-based halogen bond donors: an experimentally-verified theoretical study.
Organic & biomolecular chemistry, 2021, 19, 7611-7620
7158208 CIFC7 H12 I2 N2C 1 2/c 114.6499; 16.45897; 28.2119
90; 95.483; 90
6771.39Sysoeva, Alexandra A.; Novikov, Alexander S.; Il'in, Mikhail V.; Suslonov, Vitalii V.; Bolotin, Dmitrii S.
Predicting the catalytic activity of azolium-based halogen bond donors: an experimentally-verified theoretical study.
Organic & biomolecular chemistry, 2021, 19, 7611-7620
7158209 CIFC15 H11 F2 N O S2P 21 21 215.8983; 15.4491; 15.8136
90; 90; 90
1440.99Zhang, Yifang; Wang, Qian; Peng, Yi; Gong, Haiying; Chen, Hua; Deng, Hongmei; Hao, Jian; Wan, Wen
Metal-free, oxidative decarboxylation of aryldifluoroacetic acid with the formation of the ArS-CF<sub>2</sub> bond.
Organic & biomolecular chemistry, 2021, 19, 7024-7030
7158210 CIFC2.69 H1.85 N0 O0.15 S0.15P 21 21 2110.2144; 15.935; 17.0604
90; 90; 90
2776.86Yue, Yuanyuan; Chao, Junli; Wang, Zhiyue; Yang, Yan; Ye, Yaqing; Sun, Chunying; Guo, Xiaohui; Liu, Jianming
Electrooxidative double C-H/C-H coupling of phenols with 3-phenylbenzothiophenes: facile access to benzothiophene derivatives.
Organic & biomolecular chemistry, 2021, 19, 7156-7160
7158211 CIFC29 H24 N2 O5 SP 1 21 111.359; 12.15; 19.406
90; 94.359; 90
2670.5Hou, Xi-Qiang; Wen, Jiang-Bo; Yan, Li; Du, Da-Ming
Squaramide-catalysed asymmetric Michael addition/cyclization cascade reaction of 4-arylmethylidene-2,3-dioxopyrrolidines with 2-isothiocyanato-1-indanones.
Organic & biomolecular chemistry, 2021, 19, 7181-7185
7158212 CIFC15 H15 N O4P 1 21/n 13.9964; 38.647; 8.7063
90; 97.942; 90
1331.78Ali, Saghir; Khan, Abu T.
Metal-free synthesis of quinoline-2,4-dicarboxylate derivatives using aryl amines and acetylenedicarboxylates through a pseudo three-component reaction.
Organic & biomolecular chemistry, 2021, 19, 7041-7050
7158213 CIFC24 H19 N O3P 1 21/c 117.7971; 10.5432; 10.0972
90; 90.796; 90
1894.44Liu, Fengting; Wang, Min; Qu, Jiatong; Lu, Haifeng; Gao, Hongyin
Synthesis of non-C<sub>2</sub> symmetrical NOBIN-type biaryls through a cascade N-arylation and [3,3]-sigmatropic rearrangement from O-arylhydroxylamines and diaryliodonium salts.
Organic & biomolecular chemistry, 2021, 19, 7246-7251
7158214 CIFC30 H23 N O3P -19.4667; 10.6302; 12.236
97.174; 111.174; 92.35
1134.28Liu, Fengting; Wang, Min; Qu, Jiatong; Lu, Haifeng; Gao, Hongyin
Synthesis of non-C<sub>2</sub> symmetrical NOBIN-type biaryls through a cascade N-arylation and [3,3]-sigmatropic rearrangement from O-arylhydroxylamines and diaryliodonium salts.
Organic & biomolecular chemistry, 2021, 19, 7246-7251
7158215 CIFC22 H16 Br N O2P -18.7634; 10.22041; 10.3147
83.8073; 70.137; 83.8485
861.35Aksenov, Alexander V.; Arutiunov, Nikolai A.; Kirilov, Nikita K.; Aksenov, Dmitrii A.; Grishin, Igor Yu; Aksenov, Nicolai A.; Wang, Huifen; Du, Liqin; Betancourt, Tania; Pelly, Stephen C.; Kornienko, Alexander; Rubin, Michael
[3 + 2]-Annulation of pyridinium ylides with 1-chloro-2-nitrostyrenes unveils a tubulin polymerization inhibitor.
Organic & biomolecular chemistry, 2021, 19, 7234-7245
7158216 CIFC15 H26 O2P 21 21 216.2068; 9.6747; 23.6894
90; 90; 90
1422.52Zhang, Cun; Wang, Bianlin; Aibibula, Paruke; Zhao, Jiangyu; Aisa, Haji Akber
Enantioselective construction of substituted pyridine and a seven-membered carbocyclic skeleton: biomimetic synthesis of (-)-rupestine D, (-)-guaipyridine, (-)-epiguaipyridine, and (-)-cananodine and their stereoisomers.
Organic & biomolecular chemistry, 2021, 19, 7081-7084
7158217 CIFC14 H19 N OP 1 21 14.9824; 11.7685; 10.6674
90; 101.617; 90
612.67Zhang, Cun; Wang, Bianlin; Aibibula, Paruke; Zhao, Jiangyu; Aisa, Haji Akber
Enantioselective construction of substituted pyridine and a seven-membered carbocyclic skeleton: biomimetic synthesis of (-)-rupestine D, (-)-guaipyridine, (-)-epiguaipyridine, and (-)-cananodine and their stereoisomers.
Organic & biomolecular chemistry, 2021, 19, 7081-7084
7158218 CIFC17 H14 B F N2 O2P 1 21 111.7384; 5.679; 12.3352
90; 116.405; 90
736.5Maeda, Hiromitsu; Haketa, Yohei; Murata, Tomoki; Ohta, Eriko; Murata, Tai; Yasuda, Nobuhiro
Self-assemblies of anionic-unit-introduced anion-responsive π-electronic molecules
Organic & Biomolecular Chemistry, 2021, 19, 7369-7373
7158219 CIFC31 H26 B Cl2 F N2 O2C 1 c 15.2329; 24.0253; 21.2592
90; 95.778; 90
2659.2Maeda, Hiromitsu; Haketa, Yohei; Murata, Tomoki; Ohta, Eriko; Murata, Tai; Yasuda, Nobuhiro
Self-assemblies of anionic-unit-introduced anion-responsive π-electronic molecules
Organic & Biomolecular Chemistry, 2021, 19, 7369-7373
7158220 CIFC18 H14 B F N2 O4.5P -18.886; 11.226; 17.787
90.896; 98.176; 110.456
1641.5Maeda, Hiromitsu; Haketa, Yohei; Murata, Tomoki; Ohta, Eriko; Murata, Tai; Yasuda, Nobuhiro
Self-assemblies of anionic-unit-introduced anion-responsive π-electronic molecules
Organic & Biomolecular Chemistry, 2021, 19, 7369-7373
7158221 CIFC34.5 H30 B N2 O5.5P 1 21/c 111.069; 30.848; 17.795
90; 91.689; 90
6074Maeda, Hiromitsu; Haketa, Yohei; Murata, Tomoki; Ohta, Eriko; Murata, Tai; Yasuda, Nobuhiro
Self-assemblies of anionic-unit-introduced anion-responsive π-electronic molecules
Organic & Biomolecular Chemistry, 2021, 19, 7369-7373
7158222 CIFC18 H14 B F N2 O4P 1 21/c 15.237; 8.7976; 34.892
90; 91.923; 90
1606.7Maeda, Hiromitsu; Haketa, Yohei; Murata, Tomoki; Ohta, Eriko; Murata, Tai; Yasuda, Nobuhiro
Self-assemblies of anionic-unit-introduced anion-responsive π-electronic molecules
Organic & Biomolecular Chemistry, 2021, 19, 7369-7373
7158223 CIFC44 H69 B F N3 O6P 1 21 19.206; 20.92; 13.58
90; 98.09; 90
2589Maeda, Hiromitsu; Haketa, Yohei; Murata, Tomoki; Ohta, Eriko; Murata, Tai; Yasuda, Nobuhiro
Self-assemblies of anionic-unit-introduced anion-responsive π-electronic molecules
Organic & Biomolecular Chemistry, 2021, 19, 7369-7373
7158224 CIFC18 H14 B F N2 O4P 1 21/n 15.8897; 15.6222; 18.0449
90; 96.961; 90
1648.07Maeda, Hiromitsu; Haketa, Yohei; Murata, Tomoki; Ohta, Eriko; Murata, Tai; Yasuda, Nobuhiro
Self-assemblies of anionic-unit-introduced anion-responsive π-electronic molecules
Organic & Biomolecular Chemistry, 2021, 19, 7369-7373
7158225 CIFC20 H18 B F N2 O5P -112.248; 12.839; 14.136
109.103; 99.474; 108.353
1902.8Maeda, Hiromitsu; Haketa, Yohei; Murata, Tomoki; Ohta, Eriko; Murata, Tai; Yasuda, Nobuhiro
Self-assemblies of anionic-unit-introduced anion-responsive π-electronic molecules
Organic & Biomolecular Chemistry, 2021, 19, 7369-7373
7158226 CIFC34 H49 B F N3 O4P 1 21/n 112.2597; 18.3041; 15.13
90; 90.384; 90
3395.1Maeda, Hiromitsu; Haketa, Yohei; Murata, Tomoki; Ohta, Eriko; Murata, Tai; Yasuda, Nobuhiro
Self-assemblies of anionic-unit-introduced anion-responsive π-electronic molecules
Organic & Biomolecular Chemistry, 2021, 19, 7369-7373
7158227 CIFC41 H50 B Cl F N3 O2P 21 21 218.819; 19.343; 22.015
90; 90; 90
3755Maeda, Hiromitsu; Haketa, Yohei; Murata, Tomoki; Ohta, Eriko; Murata, Tai; Yasuda, Nobuhiro
Self-assemblies of anionic-unit-introduced anion-responsive π-electronic molecules
Organic & Biomolecular Chemistry, 2021, 19, 7369-7373
7158228 CIFC46 H46 B Cl3 F N5 O2P -110.015; 11.0473; 18.5628
88.109; 76.917; 87.736
1998.3Maeda, Hiromitsu; Haketa, Yohei; Murata, Tomoki; Ohta, Eriko; Murata, Tai; Yasuda, Nobuhiro
Self-assemblies of anionic-unit-introduced anion-responsive π-electronic molecules
Organic & Biomolecular Chemistry, 2021, 19, 7369-7373
7158229 CIFC21 H19 B N2 O5P m n 2114.507; 9.3436; 14.134
90; 90; 90
1915.8Maeda, Hiromitsu; Haketa, Yohei; Murata, Tomoki; Ohta, Eriko; Murata, Tai; Yasuda, Nobuhiro
Self-assemblies of anionic-unit-introduced anion-responsive π-electronic molecules
Organic & Biomolecular Chemistry, 2021, 19, 7369-7373
7158230 CIFC26 H17 F N2 O3P b c a6.8865; 22.291; 25.817
90; 90; 90
3963.1Yadav, Maruti B.; Jeong, Yeon Tae
A one-pot ring-closure and ring-opening sequence for the cascade synthesis of dihydrofurofurans and functionalized furans.
Organic & biomolecular chemistry, 2021, 19, 7409-7419
7158231 CIFC33 H26 N2 O4P 1 21/c 117.799; 9.2371; 18.139
90; 114.941; 90
2704.1Yadav, Maruti B.; Jeong, Yeon Tae
A one-pot ring-closure and ring-opening sequence for the cascade synthesis of dihydrofurofurans and functionalized furans.
Organic & biomolecular chemistry, 2021, 19, 7409-7419
7158232 CIFC18 H22 N2 O2P -16.2951; 7.8493; 16.3441
80.613; 85.44; 89.52
794.25Pradhan, Subham; Thiyagarajan, Subramanian; Gunanathan, Chidambaram
Ruthenium(ii)-catalysed 1,2-selective hydroboration of aldazines.
Organic & biomolecular chemistry, 2021, 19, 7147-7151
7158233 CIFC16 H17 N2 S2P 1 21/c 15.3374; 17.4593; 16.6786
90; 93.097; 90
1551.96Pradhan, Subham; Thiyagarajan, Subramanian; Gunanathan, Chidambaram
Ruthenium(ii)-catalysed 1,2-selective hydroboration of aldazines.
Organic & biomolecular chemistry, 2021, 19, 7147-7151
7158234 CIFC20 H26 N2P -18.253; 8.2551; 14.7902
94.559; 102.195; 117.627
854.1Pradhan, Subham; Thiyagarajan, Subramanian; Gunanathan, Chidambaram
Ruthenium(ii)-catalysed 1,2-selective hydroboration of aldazines.
Organic & biomolecular chemistry, 2021, 19, 7147-7151
7158235 CIFC22 H17 F3 O2P b c a16.1778; 11.4254; 18.2577
90; 90; 90
3374.7Gao, Wangxi; Niu, Lixin; Wang, Tao; Liang, Yong; Wang, Ding; Zhang, Zunting
Synthesis of cis/trans-dihydrochromenones via a photoinduced rearrangement of 4-phenyl-3-aryl/cyclohexenylcoumarins.
Organic & biomolecular chemistry, 2021, 19, 7176-7180
7158236 CIFC24 H22 N2 O5 SP 21 21 219.42743; 9.8509; 24.0927
90; 90; 90
2237.46Yang, Zinan; He, Huakang; Tian, Rui; Wu, Ruoran; Hu, Sheng; Wu, Yue; Zhou, Hui
A zinc/PyBisulidine catalyzed asymmetric Mannich reaction of N-tosyl imines with 3-acyloxy-2-oxindoles
Organic & Biomolecular Chemistry, 2021, 19, 7460-7469
7158237 CIFC32 H35 Br N O7 PP 21 21 216.4713; 9.6298; 48.285
90; 90; 90
3009Jaiswal, Manish K.; Singh, Sanjay; Singh, Ravi P.
Enantioselective vinylogous aldol reaction of acylphosphonates with 3-alkylidene oxindoles.
Organic & biomolecular chemistry, 2021, 19, 7861-7866
7158238 CIFC32 H35 Br N O7 PP 21 21 216.5171; 9.8455; 48.456
90; 90; 90
3109.1Jaiswal, Manish K.; Singh, Sanjay; Singh, Ravi P.
Enantioselective vinylogous aldol reaction of acylphosphonates with 3-alkylidene oxindoles.
Organic & biomolecular chemistry, 2021, 19, 7861-7866
7158239 CIFC19 H17 F N2 O5P 419.5302; 9.5302; 19.3236
90; 90; 90
1755.06Chen, Huiqing; Tang, Jie; Liu, Ting; Yu, Li-Fang; Xing, Dong; Yang, Fan
Enantioselective synthesis of chiral 3-alkyl-3-nitro-4-chromanones via chiral thiourea-catalysed intramolecular Michael-type cyclization.
Organic & biomolecular chemistry, 2021, 19, 7403-7408
7158240 CIFC6 H10 Br I N2P b c a11.7188; 11.8757; 13.5901
90; 90; 90
1891.3Alvarez, Marie Stacey; Houzé, Cedric; Groni, Sihem; Schöllhorn, Bernd; Fave, Claire
Halogen bonding effect on electrochemical anion oxidation in ionic liquids.
Organic & biomolecular chemistry, 2021, 19, 7587-7593
7158241 CIFC12 H20 I6 N4P b c a15.7331; 13.3955; 23.5749
90; 90; 90
4968.47Alvarez, Marie Stacey; Houzé, Cedric; Groni, Sihem; Schöllhorn, Bernd; Fave, Claire
Halogen bonding effect on electrochemical anion oxidation in ionic liquids.
Organic & biomolecular chemistry, 2021, 19, 7587-7593
7158242 CIFC13 H9 N7P 1 21/n 14.34; 25.45; 11.54
90; 99.909; 90
1255.6Tsyrenova, Biligma D.; Khrustalev, Victor N.; Nenajdenko, Valentine G.
Synthesis of blue light emitting heterocycles <i>via</i> cyclization of 2-pyridine derived 4-azido-r1,2,3-triazoles.
Organic & biomolecular chemistry, 2021, 19, 8140-8152
7158243 CIFC13 H9 N5P 1 21/n 17.2746; 13.4066; 10.9808
90; 95.693; 90
1065.6Tsyrenova, Biligma D.; Khrustalev, Victor N.; Nenajdenko, Valentine G.
Synthesis of blue light emitting heterocycles <i>via</i> cyclization of 2-pyridine derived 4-azido-r1,2,3-triazoles.
Organic & biomolecular chemistry, 2021, 19, 8140-8152
7158244 CIFC17 H11 N5P 1 21/n 16.0935; 9.7182; 22.0737
90; 90.354; 90
1307.13Tsyrenova, Biligma D.; Khrustalev, Victor N.; Nenajdenko, Valentine G.
Synthesis of blue light emitting heterocycles <i>via</i> cyclization of 2-pyridine derived 4-azido-r1,2,3-triazoles.
Organic & biomolecular chemistry, 2021, 19, 8140-8152
7158245 CIFC34 H28 I2 O4P 1 21/n 112.4916; 14.1803; 18.3463
90; 103.83; 90
3155.55Hoshi, Keita; Yasuda, Masashi; Nakamura, Takumi; Yoshida, Yasushi; Ueta, Shoko; Minagawa, Keiji; Kawamura, Yasuhiko; Imada, Yasushi; Yagishita, Fumitoshi
Unexpected formation of poly-functionalized fulvenes by the reaction of a tetraaryl[5]cumulene with iodine.
Organic & biomolecular chemistry, 2021, 19, 7594-7597
7158246 CIFC48 H42 O6C 1 2/c 123.5796; 15.5436; 11.2836
90; 102.796; 90
4032.9Hoshi, Keita; Yasuda, Masashi; Nakamura, Takumi; Yoshida, Yasushi; Ueta, Shoko; Minagawa, Keiji; Kawamura, Yasuhiko; Imada, Yasushi; Yagishita, Fumitoshi
Unexpected formation of poly-functionalized fulvenes by the reaction of a tetraaryl[5]cumulene with iodine.
Organic & biomolecular chemistry, 2021, 19, 7594-7597
7158247 CIFC34 H28 O4P 1 21 110.913; 7.442; 16.072
90; 101.62; 90
1278.5Hoshi, Keita; Yasuda, Masashi; Nakamura, Takumi; Yoshida, Yasushi; Ueta, Shoko; Minagawa, Keiji; Kawamura, Yasuhiko; Imada, Yasushi; Yagishita, Fumitoshi
Unexpected formation of poly-functionalized fulvenes by the reaction of a tetraaryl[5]cumulene with iodine.
Organic & biomolecular chemistry, 2021, 19, 7594-7597
7158248 CIFC34 H29 I O4P -110.24137; 11.9283; 13.3381
113.529; 109.913; 93.193
1369.46Hoshi, Keita; Yasuda, Masashi; Nakamura, Takumi; Yoshida, Yasushi; Ueta, Shoko; Minagawa, Keiji; Kawamura, Yasuhiko; Imada, Yasushi; Yagishita, Fumitoshi
Unexpected formation of poly-functionalized fulvenes by the reaction of a tetraaryl[5]cumulene with iodine.
Organic & biomolecular chemistry, 2021, 19, 7594-7597
7158250 CIFC21 H20 N2 O2P 21 21 2110.0469; 10.3794; 16.33
90; 90; 90
1702.91Li, Wenzhong; Wang, Yu; Qi, Huijing; Shi, Ran; Li, Jiazhu; Chen, Si; Xu, Xin-Ming; Wang, Wei-Li
Diverse privileged <i>N</i>-polycyclic skeletons accessed from a metal-free cascade cyclization reaction.
Organic & biomolecular chemistry, 2021, 19, 8086-8095
7158251 CIFC19 H18 Br N O3P 4310.7269; 10.7269; 14.5422
90; 90; 90
1673.32Li, Wenzhong; Wang, Yu; Qi, Huijing; Shi, Ran; Li, Jiazhu; Chen, Si; Xu, Xin-Ming; Wang, Wei-Li
Diverse privileged <i>N</i>-polycyclic skeletons accessed from a metal-free cascade cyclization reaction.
Organic & biomolecular chemistry, 2021, 19, 8086-8095
7158252 CIFC18 H14 N2P 1 21/n 110.6034; 12.769; 10.619
90; 110.867; 90
1343.5Yang, Kai; Luo, Shi-He; Chen, Si-Hong; Cao, Xi-Ying; Zhou, Yong-Jun; Lin, Yan-Lan; Huo, Yan-Ping; Wang, Zhao-Yang
Simple inorganic base promoted C-N and C-C formation: synthesis of benzo[4,5]imidazo[1,2-<i>a</i>]pyridines as functional AIEgens used for detecting picric acid.
Organic & biomolecular chemistry, 2021, 19, 8133-8139
7158253 CIFC23 H15 Cl N2P -19.8768; 9.9849; 10.2735
106.386; 91.697; 116.134
858.6Yang, Kai; Luo, Shi-He; Chen, Si-Hong; Cao, Xi-Ying; Zhou, Yong-Jun; Lin, Yan-Lan; Huo, Yan-Ping; Wang, Zhao-Yang
Simple inorganic base promoted C-N and C-C formation: synthesis of benzo[4,5]imidazo[1,2-<i>a</i>]pyridines as functional AIEgens used for detecting picric acid.
Organic & biomolecular chemistry, 2021, 19, 8133-8139
7158254 CIFC23 H15 N3 O2P -19.9767; 10.2; 10.3359
107.613; 91.055; 117.427
874.2Yang, Kai; Luo, Shi-He; Chen, Si-Hong; Cao, Xi-Ying; Zhou, Yong-Jun; Lin, Yan-Lan; Huo, Yan-Ping; Wang, Zhao-Yang
Simple inorganic base promoted C-N and C-C formation: synthesis of benzo[4,5]imidazo[1,2-<i>a</i>]pyridines as functional AIEgens used for detecting picric acid.
Organic & biomolecular chemistry, 2021, 19, 8133-8139
7158255 CIFC25 H19 Cl N2P 1 21/n 110.052; 10.4783; 18.7614
90; 93.129; 90
1973.2Yang, Kai; Luo, Shi-He; Chen, Si-Hong; Cao, Xi-Ying; Zhou, Yong-Jun; Lin, Yan-Lan; Huo, Yan-Ping; Wang, Zhao-Yang
Simple inorganic base promoted C-N and C-C formation: synthesis of benzo[4,5]imidazo[1,2-<i>a</i>]pyridines as functional AIEgens used for detecting picric acid.
Organic & biomolecular chemistry, 2021, 19, 8133-8139
7158256 CIFC24 H18 N2P -19.9393; 10.0786; 10.2828
106.688; 91.551; 116.591
867.6Yang, Kai; Luo, Shi-He; Chen, Si-Hong; Cao, Xi-Ying; Zhou, Yong-Jun; Lin, Yan-Lan; Huo, Yan-Ping; Wang, Zhao-Yang
Simple inorganic base promoted C-N and C-C formation: synthesis of benzo[4,5]imidazo[1,2-<i>a</i>]pyridines as functional AIEgens used for detecting picric acid.
Organic & biomolecular chemistry, 2021, 19, 8133-8139
7158257 CIFC59 H71 N O14 S5P -113.1197; 15.7488; 16.2572
103.53; 99.6156; 105.348
3054.01Landovský, Tomáš; Babor, Martin; Čejka, Jan; Eigner, Václav; Dvoƙáková, Hana; Krupička, Martin; Lhoták, Pavel
Nucleophile-induced transformation of phenoxathiin-based thiacalixarenes.
Organic & biomolecular chemistry, 2021, 19, 8075-8085
7158258 CIFC55.3 H71.91 N3.3 O16.6 S5P -113.12948; 14.11541; 19.1344
94.9881; 105.935; 114.83
3010.41Landovský, Tomáš; Babor, Martin; Čejka, Jan; Eigner, Václav; Dvoƙáková, Hana; Krupička, Martin; Lhoták, Pavel
Nucleophile-induced transformation of phenoxathiin-based thiacalixarenes.
Organic & biomolecular chemistry, 2021, 19, 8075-8085
7158259 CIFC58 H78 N4 O20 S5P -115.2602; 15.3461; 15.8961
111.084; 108.289; 93.047
3239.5Landovský, Tomáš; Babor, Martin; Čejka, Jan; Eigner, Václav; Dvoƙáková, Hana; Krupička, Martin; Lhoták, Pavel
Nucleophile-induced transformation of phenoxathiin-based thiacalixarenes.
Organic & biomolecular chemistry, 2021, 19, 8075-8085
7158260 CIFC42 H50 O12 S4P 1 21/c 115.8648; 13.9916; 19.6709
90; 95.999; 90
4342.5Landovský, Tomáš; Babor, Martin; Čejka, Jan; Eigner, Václav; Dvoƙáková, Hana; Krupička, Martin; Lhoták, Pavel
Nucleophile-induced transformation of phenoxathiin-based thiacalixarenes.
Organic & biomolecular chemistry, 2021, 19, 8075-8085
7158261 CIFC48 H64 O12 S5P -113.7779; 14.4703; 14.6125
81.1803; 76.6391; 63.6398
2535.42Landovský, Tomáš; Babor, Martin; Čejka, Jan; Eigner, Václav; Dvoƙáková, Hana; Krupička, Martin; Lhoták, Pavel
Nucleophile-induced transformation of phenoxathiin-based thiacalixarenes.
Organic & biomolecular chemistry, 2021, 19, 8075-8085
7158262 CIFC33 H32 OP b c n36.302; 17.985; 8.873
90; 90; 90
5793Feng, Yi-Man; Nie, Xiao-Di; Sun, Jian-Ting; Xu, Wen-Ke; Wei, Bang-Guo
TMSOTf-mediated synthesis of skipped dienes through the addition of olefins to imines and semicyclic <i>N</i>,<i>O</i>-acetals.
Organic & biomolecular chemistry, 2021, 19, 7883-7893
7158263 CIFC35 H27 FP b c a18.4643; 8.6875; 32.046
90; 90; 90
5140.5Feng, Yi-Man; Nie, Xiao-Di; Sun, Jian-Ting; Xu, Wen-Ke; Wei, Bang-Guo
TMSOTf-mediated synthesis of skipped dienes through the addition of olefins to imines and semicyclic <i>N</i>,<i>O</i>-acetals.
Organic & biomolecular chemistry, 2021, 19, 7883-7893
7158264 CIFC9 H14 Br N O3P -14.5418; 10.9707; 11.8989
109.638; 92.037; 101.081
544.76Chen, Xiao Yun; Yuan, Shuxia; Chen, Yan; Sun, Chenyang; Tang, Yaonan; Chen, Guang; Zhu, Baocheng; Chen, Kaiwei; Zheng, Shaojun; Cheng, Xiaofang
Solvent-controlled two-step one-pot syntheses of α-X (X = Br or Cl) enamino ketones/esters and 3-(2,5-dioxopyrrolidin-1-yl)acrylate by using terminal carbonyl alkynes.
Organic & biomolecular chemistry, 2021, 19, 7914-7919
7158265 CIFC13 H13 N O2P 1 21 18.8556; 6.92143; 9.428
90; 111.887; 90
536.22Ma, Haowen; Feng, Jiajie; Zhou, Wei; Chen, Chen; Deng, Zhuoji; Zhou, Fengtao; Ouyang, Yifan; Zhang, Xinhao; Cai, Qian
Copper(i)-catalyzed asymmetric intramolecular C-arylation with ureas as the additives: highly enantioselective formation of spirooxindoles
Organic & Biomolecular Chemistry, 2021, 19, 7480-7484
7158266 CIFC13 H13 N O4P 21 21 216.94293; 9.02763; 18.0531
90; 90; 90
1131.54Ma, Haowen; Feng, Jiajie; Zhou, Wei; Chen, Chen; Deng, Zhuoji; Zhou, Fengtao; Ouyang, Yifan; Zhang, Xinhao; Cai, Qian
Copper(i)-catalyzed asymmetric intramolecular C-arylation with ureas as the additives: highly enantioselective formation of spirooxindoles
Organic & Biomolecular Chemistry, 2021, 19, 7480-7484
7158267 CIFC13 H14 N2 O2P 21 21 216.956; 8.4636; 19.6496
90; 90; 90
1156.83Ma, Haowen; Feng, Jiajie; Zhou, Wei; Chen, Chen; Deng, Zhuoji; Zhou, Fengtao; Ouyang, Yifan; Zhang, Xinhao; Cai, Qian
Copper(i)-catalyzed asymmetric intramolecular C-arylation with ureas as the additives: highly enantioselective formation of spirooxindoles
Organic & Biomolecular Chemistry, 2021, 19, 7480-7484
7158268 CIFC24 H18 N2 O SP 1 21 16.8325; 15.642; 8.9374
90; 92.861; 90
953.98Li, Chen-Yi; Xiang, Min; Zhang, Jian; Li, Wen-Sheng; Zou, Ying; Tian, Fang; Wang, Li-Xin
Organocatalytic enantioselective aza-Friedel-Crafts reaction between benzothiazolimines and 2-naphthols for the preparation of chiral 2'-aminobenzothiazolomethyl naphthols.
Organic & biomolecular chemistry, 2021, 19, 7690-7694
7158269 CIFC10 H14 N4P -17.5321; 8.0983; 9.2836
71.4315; 73.3773; 66.8118
484.97Al Isawi, Wisam A.; Salome, Austin Z.; Ahmed, Basil M.; Zeller, Matthias; Mezei, Gellert
Selective binding of anions by rigidified nanojars: sulfate <i>vs.</i> carbonate.
Organic & biomolecular chemistry, 2021, 19, 7641-7654
7158270 CIFC20 H30 N4 O2P 1 21/c 116.5743; 4.646; 12.7547
90; 97.57; 90
973.61Al Isawi, Wisam A.; Salome, Austin Z.; Ahmed, Basil M.; Zeller, Matthias; Mezei, Gellert
Selective binding of anions by rigidified nanojars: sulfate <i>vs.</i> carbonate.
Organic & biomolecular chemistry, 2021, 19, 7641-7654
7158271 CIFC21 H32 N4 O2P -18.297; 9.2575; 15.0135
87.5026; 80.0574; 64.7954
1027.14Al Isawi, Wisam A.; Salome, Austin Z.; Ahmed, Basil M.; Zeller, Matthias; Mezei, Gellert
Selective binding of anions by rigidified nanojars: sulfate <i>vs.</i> carbonate.
Organic & biomolecular chemistry, 2021, 19, 7641-7654
7158272 CIFC15 H12 Cl F3 O2 S2P 1 21/c 18.7553; 6.4721; 28.2921
90; 97.357; 90
1589.98Li, Jiuling; Li, Bin; Chen, Juan; Jia, Xinyu; Wang, Min; Hao, Chengjun; Zheng, Xinhua; Dai, Hongmei; Hu, Wenhao
Catalyst-free <i>gem</i>-chlorosulfurization of difluoromethyl-substituted diazo compounds with disulfide and PhICl<sub>2</sub>.
Organic & biomolecular chemistry, 2021, 19, 8030-8034
7158273 CIFC22 H20 Br N O5P -17.7741; 11.2133; 13.2379
71.466; 74.538; 81.457
1051.97Ramos-Orea, Aldahir; Ramírez-Apan, Teresa; Chávez-Santos, Rosa María; Aguayo-Ortiz, Rodrigo; Espitia, Clara; Silva Miranda, Mayra; Torres-Ochoa, Rubén O; Martínez, Roberto
Total syntheses and antiproliferative activities of prenostodione and its analogues.
Organic & biomolecular chemistry, 2021, 19, 8272-8280
7158274 CIFC12 H10 F2 N2 O3P 1 21/c 16.2592; 14.9217; 13.9603
90; 95.929; 90
1296.89Wang, Qian; Gong, Haiying; Zhang, Yifang; Peng, Yi; Chen, Hua; Li, Mingjie; Deng, Hongmei; Hao, Jian; Wan, Wen
Visible-light mediated stereospecific C(sp<sup>2</sup>)-H difluoroalkylation of (<i>Z</i>)-aldoximes.
Organic & biomolecular chemistry, 2021, 19, 7867-7874
7158275 CIFC32 H38 N2 O10P -17.2273; 10.1947; 10.5388
90.94; 96.739; 101.524
754.96Rao, Maddali L. N.; Islam, Sk Shamim; Dasgupta, Priyabrata
Copper-catalyzed domino synthesis of ynamines.
Organic & biomolecular chemistry, 2021, 19, 7855-7860
7158276 CIFC21 H17 Cl N2 O4C 1 2/c 127.3068; 7.9003; 18.7137
90; 108.028; 90
3838.9Ramaraju, Andhavaram; Upare, Atul; Blanch, Ewan W.; Maniam, Subashani; Sridhar, Balasubramanian; Bathula, Surendar Reddy; Raji Reddy, Chada
Chemoselective [3 + 2] annulation of oxime acetate with 2-aryl-3-ethoxycarbonyl-pyrroline-4,5-dione: an entry to pyrrolo[2,3-<i>b</i>]pyrrole derivatives.
Organic & biomolecular chemistry, 2021, 19, 7875-7882
7158277 CIFC22 H16 N2 O2P 1 21/c 119.2136; 10.6907; 8.1348
90; 98.4; 90
1653.02Liao, Shengrong; Xu, Huayan; Yang, Bin; Wang, Junfeng; Zhou, Xuefeng; Lin, Xiuping; Liu, Yonghong
Gold-catalyzed oxidation of terminal alkynes to glyoxals and their reactions with 2-phenylimidazo[1,2-<i>a</i>]pyridines: one-pot synthesis of 1,2-diones.
Organic & biomolecular chemistry, 2021, 19, 8735-8739
7158278 CIFC19 H19 N O2P 21 21 225.3513; 13.438; 9.4134
90; 90; 90
3206.9Solea, Atena B.; Wang, Sining; Xue, Xiao-Song; Crochet, Aurelien; Fromm, Katharina M.; Houk, Kendall N.; Mamula, Olimpia; Allemann, Christophe
Efficient synthesis of isoindolones by intramolecular cyclisation of pyridinylbenzoic acids.
Organic & biomolecular chemistry, 2021, 19, 8025-8029
7158279 CIFC13 H11 N O2P n a 2113.0488; 7.7427; 10.6551
90; 90; 90
1076.52Solea, Atena B.; Wang, Sining; Xue, Xiao-Song; Crochet, Aurelien; Fromm, Katharina M.; Houk, Kendall N.; Mamula, Olimpia; Allemann, Christophe
Efficient synthesis of isoindolones by intramolecular cyclisation of pyridinylbenzoic acids.
Organic & biomolecular chemistry, 2021, 19, 8025-8029
7158280 CIFC19 H17 N OP 21 21 217.0872; 12.3506; 16.599
90; 90; 90
1452.9Solea, Atena B.; Wang, Sining; Xue, Xiao-Song; Crochet, Aurelien; Fromm, Katharina M.; Houk, Kendall N.; Mamula, Olimpia; Allemann, Christophe
Efficient synthesis of isoindolones by intramolecular cyclisation of pyridinylbenzoic acids.
Organic & biomolecular chemistry, 2021, 19, 8025-8029
7158281 CIFC34 H36 O2P -14.787; 13.87; 21.66
72.77; 90; 90
1374Chinnabattigalla, Sreenivasulu; Choudhury, Aditya; Gedu, Satyanarayana
[Pd]-Catalyzed <i>para</i>-selective allylation of phenols: access to 4-[(<i>E</i>)-3-aryl/alkylprop-2-enyl]phenols.
Organic & biomolecular chemistry, 2021, 19, 8259-8263
7158282 CIFC19 H22 O4P -18.4709; 9.983; 11.1522
72.48; 75.864; 69.734
833.28Chinnabattigalla, Sreenivasulu; Choudhury, Aditya; Gedu, Satyanarayana
[Pd]-Catalyzed <i>para</i>-selective allylation of phenols: access to 4-[(<i>E</i>)-3-aryl/alkylprop-2-enyl]phenols.
Organic & biomolecular chemistry, 2021, 19, 8259-8263
7158283 CIFC17 H17 Br OP 1 21 18.2775; 5.2464; 17.4065
90; 92.906; 90
754.94Chinnabattigalla, Sreenivasulu; Choudhury, Aditya; Gedu, Satyanarayana
[Pd]-Catalyzed <i>para</i>-selective allylation of phenols: access to 4-[(<i>E</i>)-3-aryl/alkylprop-2-enyl]phenols.
Organic & biomolecular chemistry, 2021, 19, 8259-8263
7158284 CIFC21 H17 F3 O2P 1 21/n 110.3698; 12.1098; 29.2861
90; 92.224; 90
3674.9Priyanka, Chiliveru; Subbarao, Muppidi; Punna, Nagender
Palladium-catalyzed <i>ortho</i>-vinylation of β-naphthols with α-trifluoromethyl allyl carbonates: one-pot access to naphtho[2,1-<i>b</i>]furans.
Organic & biomolecular chemistry, 2021, 19, 8241-8245
7158285 CIFC H Cl N O SP -17.0134; 7.0858; 15.5319
96.28; 90.168; 104.398
742.77Singh, Rashmi; Sharma, Vishal Prasad; Yadav, Priyanka; Sonker, Priyanka; Singh, Radhey Mohan; Tewari, Ashish Kumar
Sodium sulphide promoted synthesis of fused quinoline at room temperature.
Organic & biomolecular chemistry, 2021, 19, 8108-8112
7158286 CIFC19 H14 N2 O2I 41/a :229.725; 29.725; 7.0358
90; 90; 90
6216.7Singh, Rashmi; Sharma, Vishal Prasad; Yadav, Priyanka; Sonker, Priyanka; Singh, Radhey Mohan; Tewari, Ashish Kumar
Sodium sulphide promoted synthesis of fused quinoline at room temperature.
Organic & biomolecular chemistry, 2021, 19, 8108-8112
7158287 CIFC35 H23 Br O6P 1 21 16.59045; 19.69096; 23.49012
90; 90; 90
3048.37Yan, Juzhang; Zheng, Xiurong; Zheng, Yangqing; Zhan, Ruoting; Huang, Huicai
Asymmetric Michael reaction of 3-homoacyl coumarins with chromone-fused dienes toward enantioenriched coumarin chromone skeletons.
Organic & biomolecular chemistry, 2021, 19, 8102-8107
7158288 CIFC17 H16 N4 OP -18.1289; 10.9783; 17.3875
82.153; 79.194; 71.829
1443.1Honnanayakanavar, Jyoti M.; Nanubolu, Jagadeesh Babu; Suresh, Surisetti
Tandem copper catalyzed regioselective <i>N</i>-arylation-amidation: synthesis of angularly fused dihydroimidazoquinazolinones and the anticancer agent TIC10/ONC201.
Organic & biomolecular chemistry, 2021, 19, 8497-8501
7158289 CIFC16 H14 N4 OP 21 21 218.275; 9.736; 16.38
90; 90; 90
1320Honnanayakanavar, Jyoti M.; Nanubolu, Jagadeesh Babu; Suresh, Surisetti
Tandem copper catalyzed regioselective <i>N</i>-arylation-amidation: synthesis of angularly fused dihydroimidazoquinazolinones and the anticancer agent TIC10/ONC201.
Organic & biomolecular chemistry, 2021, 19, 8497-8501
7158290 CIFC18 H17 N3 OP 1 21/c 17.6364; 24.214; 8.2875
90; 108.818; 90
1450.5Honnanayakanavar, Jyoti M.; Nanubolu, Jagadeesh Babu; Suresh, Surisetti
Tandem copper catalyzed regioselective <i>N</i>-arylation-amidation: synthesis of angularly fused dihydroimidazoquinazolinones and the anticancer agent TIC10/ONC201.
Organic & biomolecular chemistry, 2021, 19, 8497-8501
7158291 CIFC17 H15 N3 OP -17.061; 16.611; 19.595
65.759; 87.399; 80.205
2064.3Honnanayakanavar, Jyoti M.; Nanubolu, Jagadeesh Babu; Suresh, Surisetti
Tandem copper catalyzed regioselective <i>N</i>-arylation-amidation: synthesis of angularly fused dihydroimidazoquinazolinones and the anticancer agent TIC10/ONC201.
Organic & biomolecular chemistry, 2021, 19, 8497-8501
7158292 CIFC16 H26 N6 O9P 1 21/c 18.7091; 24.6511; 9.7352
90; 94.492; 90
2083.6Lohrman, Jessica; Pramanik, Subhamay; Kaur, Sandeep; Telikepalli, Hanumaiah; Day, Victor W.; Bowman-James, Kristin
Hydrophilic and hydrophobic carboxamide pincers as anion hosts.
Organic & biomolecular chemistry, 2021, 19, 8516-8520
7158293 CIFC32 H56 N6 O4C 1 2/c 144.553; 4.9317; 15.7652
90; 90.399; 90
3463.9Lohrman, Jessica; Pramanik, Subhamay; Kaur, Sandeep; Telikepalli, Hanumaiah; Day, Victor W.; Bowman-James, Kristin
Hydrophilic and hydrophobic carboxamide pincers as anion hosts.
Organic & biomolecular chemistry, 2021, 19, 8516-8520
7158294 CIFC24 H40 N6 O12P 1 21/c 111.0587; 14.955; 8.8548
90; 101.133; 90
1436.9Lohrman, Jessica; Pramanik, Subhamay; Kaur, Sandeep; Telikepalli, Hanumaiah; Day, Victor W.; Bowman-James, Kristin
Hydrophilic and hydrophobic carboxamide pincers as anion hosts.
Organic & biomolecular chemistry, 2021, 19, 8516-8520
7158295 CIFC20 H27 N3 OP -110.9301; 12.0124; 16.8138
69.946; 72.758; 64.698
1845.4Bormann, Carl Thomas; Fadaei-Tirani, Farzaneh; Scopelliti, Rosario; Severin, Kay
Synthesis of bicyclic vinyl triazenes by Ficini-type reactions.
Organic & biomolecular chemistry, 2021, 19, 8113-8117
7158296 CIFC26 H36 N4 O3 SP 1 21/c 17.80574; 34.1537; 9.6271
90; 95.7493; 90
2553.63Bormann, Carl Thomas; Fadaei-Tirani, Farzaneh; Scopelliti, Rosario; Severin, Kay
Synthesis of bicyclic vinyl triazenes by Ficini-type reactions.
Organic & biomolecular chemistry, 2021, 19, 8113-8117
7158297 CIFC15 H18 N2 O2 SP 1 21/c 19.3141; 7.60332; 20.7811
90; 93.9407; 90
1468.2Bandyopadhyay, Debashruti; Thirupathi, Annaram; Radhakrishnan, Divya; Panigrahi, Adyasha; Peruncheralathan, S.
Triflic acid-mediated N-heteroannulation of β-anilino-β-(methylthio)acrylonitriles: a facile synthesis of 4-amino-2-(methylthio)quinolines.
Organic & biomolecular chemistry, 2021, 19, 8544-8553
7158298 CIFC31 H31 N7 O9 S2P 1 21/n 111.069; 19.863; 14.418
90; 93.29; 90
3164.8McNaughton, Daniel A.; Macreadie, Lauren K.; Gale, Philip A.
Acridinone-based anion transporters.
Organic & biomolecular chemistry, 2021, 19, 9659-9674
7158299 CIFC22 H16 Br N3 O2P 16.062; 12.279; 13.666
75.605; 86.331; 89.054
983.3Wang, Yu; Niu, Cheng; Xie, Dong-Hua; Du, Da-Ming
A bifunctional squaramide-catalysed enantioselective vinylogous Michael addition/cyclization cascade reaction of 4-unsaturated isoxazol-5-ones and α,α-dicyanoalkenes.
Organic & biomolecular chemistry, 2021, 19, 8572-8577
7158300 CIFC29 H24 Br F3 N2 O5P 17.0824; 9.9984; 11.3089
113.621; 101.541; 100.342
688.15Wang, Rui-Li; Jia, Shi-Kun; Guo, Ya-Jun; Yi, Yang; Hua, Yuan-Zhao; Lu, Hui-Jie; Wang, Min-Can
Dinuclear zinc-catalyzed enantioselective formal [3 + 2] cycloaddition of <i>N</i>-2,2,2-trifluoroethylisatin ketimines with low reactivity aurone derivatives.
Organic & biomolecular chemistry, 2021, 19, 8492-8496
7158301 CIFC24 H26 O4P 21 21 2110.0685; 10.1743; 20.3368
90; 90; 90
2083.3Rithchumpon, Puracheth; Intakaew, Neeranuth; Khamto, Nopawit; Yimklan, Saranpong; Nimmanpipug, Piyarat; Thavornyutikarn, Praput; Meepowpan, Puttinan
Synthesis and application of methyl itaconate-anthracene adducts in configuration assignment of chiral secondary alcohols by <sup>1</sup>H NMR.
Organic & biomolecular chemistry, 2021, 19, 8955-8967
7158302 CIFC24 H25 O4P 21 21 2110.1003; 10.1984; 20.2551
90; 90; 90
2086.42Rithchumpon, Puracheth; Intakaew, Neeranuth; Khamto, Nopawit; Yimklan, Saranpong; Nimmanpipug, Piyarat; Thavornyutikarn, Praput; Meepowpan, Puttinan
Synthesis and application of methyl itaconate-anthracene adducts in configuration assignment of chiral secondary alcohols by <sup>1</sup>H NMR.
Organic & biomolecular chemistry, 2021, 19, 8955-8967
7158303 CIFC24 H26 O4P 21 21 2110.1047; 10.1997; 20.2588
90; 90; 90
2087.97Rithchumpon, Puracheth; Intakaew, Neeranuth; Khamto, Nopawit; Yimklan, Saranpong; Nimmanpipug, Piyarat; Thavornyutikarn, Praput; Meepowpan, Puttinan
Synthesis and application of methyl itaconate-anthracene adducts in configuration assignment of chiral secondary alcohols by <sup>1</sup>H NMR.
Organic & biomolecular chemistry, 2021, 19, 8955-8967
7158304 CIFC24 H26 O4P 21 21 2110.0659; 10.174; 20.3251
90; 90; 90
2081.5Rithchumpon, Puracheth; Intakaew, Neeranuth; Khamto, Nopawit; Yimklan, Saranpong; Nimmanpipug, Piyarat; Thavornyutikarn, Praput; Meepowpan, Puttinan
Synthesis and application of methyl itaconate-anthracene adducts in configuration assignment of chiral secondary alcohols by <sup>1</sup>H NMR.
Organic & biomolecular chemistry, 2021, 19, 8955-8967
7158305 CIFC20 H20 O S2P 1 21/c 19.8031; 12.4858; 14.4741
90; 100.794; 90
1740.28Zhang, Shan-Shan; Xue, Jiahui; Gu, Qing; Jiang, Xuefeng; You, Shu-Li
Dearomatization reaction of β-naphthols with disulfurating reagents.
Organic & biomolecular chemistry, 2021, 19, 8761-8771
7158306 CIFC20 H19 N O S2P 1 21/c 19.8601; 11.9035; 15.2689
90; 101.418; 90
1756.64Zhang, Shan-Shan; Xue, Jiahui; Gu, Qing; Jiang, Xuefeng; You, Shu-Li
Dearomatization reaction of β-naphthols with disulfurating reagents.
Organic & biomolecular chemistry, 2021, 19, 8761-8771
7158307 CIFC36 H29 Cl N2 O5 S2P 1 21/n 18.4201; 11.3961; 33.642
90; 95.484; 90
3213.4Zeng, Wenlei; Yu, Aimin; Meng, Xiangtai
Catalyst-controlled switchable [4 + 1], [4 + 3] and [3 + 2] domino reactions of azadienes and MBH carbonates: diverse synthesis of benzothiophene fused derivatives.
Organic & biomolecular chemistry, 2021, 19, 8783-8788
7158308 CIFC36 H30 Cl N2 O5 S2P 1 21/c 110.3934; 18.0084; 17.5835
90; 97.424; 90
3263.49Zeng, Wenlei; Yu, Aimin; Meng, Xiangtai
Catalyst-controlled switchable [4 + 1], [4 + 3] and [3 + 2] domino reactions of azadienes and MBH carbonates: diverse synthesis of benzothiophene fused derivatives.
Organic & biomolecular chemistry, 2021, 19, 8783-8788
7158309 CIFC36 H31 Cl N2 O5 S2I 1 2/a 123.2429; 9.7717; 28.6043
90; 94.72; 90
6474.7Zeng, Wenlei; Yu, Aimin; Meng, Xiangtai
Catalyst-controlled switchable [4 + 1], [4 + 3] and [3 + 2] domino reactions of azadienes and MBH carbonates: diverse synthesis of benzothiophene fused derivatives.
Organic & biomolecular chemistry, 2021, 19, 8783-8788
7158310 CIFC36 H29 Cl N2 O5 S2P 1 21/c 19.0939; 30.322; 11.9757
90; 92.92; 90
3298Zeng, Wenlei; Yu, Aimin; Meng, Xiangtai
Catalyst-controlled switchable [4 + 1], [4 + 3] and [3 + 2] domino reactions of azadienes and MBH carbonates: diverse synthesis of benzothiophene fused derivatives.
Organic & biomolecular chemistry, 2021, 19, 8783-8788
7158311 CIFC36 H29 Cl N2 O7 S2P -110.8359; 11.1243; 17.4373
86.651; 78.773; 67.019
1897.71Zeng, Wenlei; Yu, Aimin; Meng, Xiangtai
Catalyst-controlled switchable [4 + 1], [4 + 3] and [3 + 2] domino reactions of azadienes and MBH carbonates: diverse synthesis of benzothiophene fused derivatives.
Organic & biomolecular chemistry, 2021, 19, 8783-8788
7158312 CIFC36 H29 Cl N2 O7 S2C 1 2/c 128.3232; 11.8905; 26.1613
90; 114.144; 90
8039.8Zeng, Wenlei; Yu, Aimin; Meng, Xiangtai
Catalyst-controlled switchable [4 + 1], [4 + 3] and [3 + 2] domino reactions of azadienes and MBH carbonates: diverse synthesis of benzothiophene fused derivatives.
Organic & biomolecular chemistry, 2021, 19, 8783-8788
7158313 CIFC36 H29 Cl N2 O5 S2P 1 21/c 121.0158; 10.2669; 18.2254
90; 108.556; 90
3728Zeng, Wenlei; Yu, Aimin; Meng, Xiangtai
Catalyst-controlled switchable [4 + 1], [4 + 3] and [3 + 2] domino reactions of azadienes and MBH carbonates: diverse synthesis of benzothiophene fused derivatives.
Organic & biomolecular chemistry, 2021, 19, 8783-8788
7158314 CIFC43 H34 N4 OP b c a18.8089; 17.8043; 21.9597
90; 90; 90
7353.8Nawaz, Shah; Huang, Yue; Bao, Xiaoze; Wei, Shiqiang; Wei, Xingfu; Qu, Jingping; Wang, Baomin
Construction of a spiro[pyrazolone-4,2'-pyridoindole] scaffold <i>via</i> a [3 + 3] cycloaddition of 2-indolylmethanol with a 4-aminopyrazolone-derived azomethine ylide.
Organic & biomolecular chemistry, 2021, 19, 8530-8538
7158315 CIFC43 H30 Cl4 N2P 1 21/n 113.9191; 12.836; 20.3504
90; 106.316; 90
3489.49Tang, Zhicong; Hong, Gang; Hu, Chen; Wang, Qi; Zhong, Yi; Gong, Yu; Yang, Peng; Wang, Limin
La(OTf)<sub>3</sub> facilitated self-condensation of 2-indolylmethanol: construction of highly substituted indeno[1,2-<i>b</i>]indoles.
Organic & biomolecular chemistry, 2021, 19, 10337-10342
7158316 CIFC46 H26 F12 N2P -112.1173; 13.979; 17.7969
78.96; 80.192; 68.596
2738Tang, Zhicong; Hong, Gang; Hu, Chen; Wang, Qi; Zhong, Yi; Gong, Yu; Yang, Peng; Wang, Limin
La(OTf)<sub>3</sub> facilitated self-condensation of 2-indolylmethanol: construction of highly substituted indeno[1,2-<i>b</i>]indoles.
Organic & biomolecular chemistry, 2021, 19, 10337-10342
7158317 CIFC31 H53 Ca Cl3 I2 N8 O12P 1 21/n 115.2822; 20.3116; 16.7995
90; 117.084; 90
4642.8Zhu, Jun; Wang, Xu-Dong; Luo, Jian; Ao, Yu-Fei; Wang, Qi-Qiang; Wang, De-Xian
Cation-chloride cotransport mediated by an ion pair transporter.
Organic & biomolecular chemistry, 2021, 19, 8586-8590
7158318 CIFC17 H11 Br F3 N O3 SP 1 21/c 118.868; 12.831; 7.106
90; 93.222; 90
1717.6Su, Shixuan; Yan, Zhipeng; Ye, Xingyuan; Wang, Jingyang; Li, Yuan; He, Guangke
PhI(OAc)2-mediated trifluoromethylthiolation/oxidative cyclization of ynamides
Organic & Biomolecular Chemistry, 2021, 19, 8746-8753
7158319 CIFC41 H42 N4 O3P 21 21 215.516; 19.977; 30.8
90; 90; 90
3393.9Kozhemyakin, Grigory L.; Tyurin, Vladimir S.; Shkirdova, Alena O.; Belyaev, Evgeny S.; Kirinova, Ekaterina S.; Ponomarev, Gelii V.; Chistov, Alexey A.; Aralov, Andrey V.; Tafeenko, Victor A.; Zamilatskov, Ilya A.
Carbene functionalization of porphyrinoids through tosylhydrazones.
Organic & biomolecular chemistry, 2021, 19, 9199-9210
7158320 CIFC24 H24 N O2 PP 1 21/c 111.7785; 17.1967; 11.2241
90; 115.786; 90
2047.1Popovics-Tóth, Nóra; Rávai, Bettina; Tajti, Ádám; Varga, Bence; Bagi, Péter; Perdih, Franc; Szabó, Pál Tamás; Hackler, Jr, László; Puskás, László G; Bálint, Erika
Three-component synthesis, utilization and biological activity of phosphinoyl-functionalized isoindolinones.
Organic & biomolecular chemistry, 2021, 19, 8754-8760
7158321 CIFC48 H48 Cl2 N2 O2 P2 PtP 1 21/n 111.3292; 10.3205; 18.9713
90; 106.63; 90
2125.4Popovics-Tóth, Nóra; Rávai, Bettina; Tajti, Ádám; Varga, Bence; Bagi, Péter; Perdih, Franc; Szabó, Pál Tamás; Hackler, Jr, László; Puskás, László G; Bálint, Erika
Three-component synthesis, utilization and biological activity of phosphinoyl-functionalized isoindolinones.
Organic & biomolecular chemistry, 2021, 19, 8754-8760
7158322 CIFC29 H27 N O5 SP -110.9106; 11.628; 11.7739
97.036; 110.448; 105.848
1306.5Shen, Jinhui; Yu, Aimin; Meng, Xiangtai
Stereoselective [4 + 3] annulation of azadienes and ethyl 4-bromo-3-oxobutanoate: construction of benzindeno-fused azepine derivatives.
Organic & biomolecular chemistry, 2021, 19, 9026-9030
7158323 CIFC28 H25 N O5 S2P -18.3217; 10.3997; 15.418
84.83; 78.631; 85.649
1300.5Shen, Jinhui; Yu, Aimin; Meng, Xiangtai
Stereoselective [4 + 3] annulation of azadienes and ethyl 4-bromo-3-oxobutanoate: construction of benzindeno-fused azepine derivatives.
Organic & biomolecular chemistry, 2021, 19, 9026-9030
7158324 CIFC29 H29 N O5 SP 1 21/n 111.0425; 16.3615; 14.8646
90; 102.389; 90
2623.08Shen, Jinhui; Yu, Aimin; Meng, Xiangtai
Stereoselective [4 + 3] annulation of azadienes and ethyl 4-bromo-3-oxobutanoate: construction of benzindeno-fused azepine derivatives.
Organic & biomolecular chemistry, 2021, 19, 9026-9030
7158325 CIFC29 H27 N O7 SP -18.1947; 13.0078; 13.8955
112.119; 96.231; 100.047
1326.27Shen, Jinhui; Yu, Aimin; Meng, Xiangtai
Stereoselective [4 + 3] annulation of azadienes and ethyl 4-bromo-3-oxobutanoate: construction of benzindeno-fused azepine derivatives.
Organic & biomolecular chemistry, 2021, 19, 9026-9030
7158326 CIFC58 H58 N2 O10 S2P -111.7154; 12.1997; 18.576
81.916; 82.255; 78.778
2562.51Shen, Jinhui; Yu, Aimin; Meng, Xiangtai
Stereoselective [4 + 3] annulation of azadienes and ethyl 4-bromo-3-oxobutanoate: construction of benzindeno-fused azepine derivatives.
Organic & biomolecular chemistry, 2021, 19, 9026-9030
7158327 CIFC27 H32.65 Cl Ir N O1.32 PP 21 21 2112.8894; 13.1148; 14.7203
90; 90; 90
2488.3Dai, Zengjin; Pan, Ying-Min; Wang, Shou-Guo; Zhang, Xumu; Yin, Qin
Direct reductive amination of ketones with ammonium salt catalysed by Cp*Ir(III) complexes bearing an amidato ligand.
Organic & biomolecular chemistry, 2021, 19, 8934-8939
7158328 CIFC18 H18 N2 O2P 1 21/c 16.5607; 7.5167; 28.7149
90; 95.426; 90
1409.72Marras, Valentina; Caboni, Pierluigi; Secci, Francesco; Guillot, Régis; Aitken, David J.; Frongia, Angelo
A Brønsted acid catalyzed tandem reaction for the diastereoselective synthesis of cyclobuta-fused tetrahydroquinoline carboxylic esters.
Organic & biomolecular chemistry, 2021, 19, 8912-8916
7158329 CIFC22 H26 N2 O2P 1 21 111.1401; 28.7617; 11.7457
90; 90.521; 90
3763.26Marras, Valentina; Caboni, Pierluigi; Secci, Francesco; Guillot, Régis; Aitken, David J.; Frongia, Angelo
A Brønsted acid catalyzed tandem reaction for the diastereoselective synthesis of cyclobuta-fused tetrahydroquinoline carboxylic esters.
Organic & biomolecular chemistry, 2021, 19, 8912-8916
7158330 CIFC23 H22 Br N3 O SP -19.087; 10.0635; 13.3909
80.956; 81.422; 65.23
1093.3Paysant, Hippolyte; Hedir, Siham; Justaud, Frédéric; Weiswald, Louis Bastien; El Dine, Assaad Nasr; Soulieman, Ali; Hachem, Ali; Elie, Nicolas; Brotin, Emilie; Denoyelle, Christophe; Bignon, Jérôme; Roussi, Fanny; Jouanne, Marie; Tasseau, Olivier; Roisnel, Thierry; Voisin-Chiret, Anne Sophie; Grée, René; Levoin, Nicolas; Poulain, Laurent
Structural revision of the Mcl-1 inhibitor MIM1: synthesis and biological studies on ovarian cancer cells with evaluation of designed analogues.
Organic & biomolecular chemistry, 2021, 19, 8968-8987
7158331 CIFC23 H20 Br N3 O SF d d 224.627; 40.014; 9.3291
90; 90; 90
9193.1Paysant, Hippolyte; Hedir, Siham; Justaud, Frédéric; Weiswald, Louis Bastien; El Dine, Assaad Nasr; Soulieman, Ali; Hachem, Ali; Elie, Nicolas; Brotin, Emilie; Denoyelle, Christophe; Bignon, Jérôme; Roussi, Fanny; Jouanne, Marie; Tasseau, Olivier; Roisnel, Thierry; Voisin-Chiret, Anne Sophie; Grée, René; Levoin, Nicolas; Poulain, Laurent
Structural revision of the Mcl-1 inhibitor MIM1: synthesis and biological studies on ovarian cancer cells with evaluation of designed analogues.
Organic & biomolecular chemistry, 2021, 19, 8968-8987
7158332 CIFC20 H28 Cl N3 O3 SP 1 21/n 17.8822; 31.959; 9.896
90; 121.156; 90
2133.3Paysant, Hippolyte; Hedir, Siham; Justaud, Frédéric; Weiswald, Louis Bastien; El Dine, Assaad Nasr; Soulieman, Ali; Hachem, Ali; Elie, Nicolas; Brotin, Emilie; Denoyelle, Christophe; Bignon, Jérôme; Roussi, Fanny; Jouanne, Marie; Tasseau, Olivier; Roisnel, Thierry; Voisin-Chiret, Anne Sophie; Grée, René; Levoin, Nicolas; Poulain, Laurent
Structural revision of the Mcl-1 inhibitor MIM1: synthesis and biological studies on ovarian cancer cells with evaluation of designed analogues.
Organic & biomolecular chemistry, 2021, 19, 8968-8987
7158333 CIFC15 H14 N4 SP 1 21/n 18.3093; 7.7536; 21.1019
90; 94.235; 90
1355.82Kutasevich, Anton V.; Niktarov, Anton S.; Uvarova, Ekaterina S.; Karnoukhova, Valentina A.; Mityanov, Vitaly S.
A novel approach to bis(1,3-azol-2-yl)acetonitriles and bis(1,3-azol-2-yl)methanes <i>via</i> the [3 + 2]-dipolar cycloaddition of imidazole <i>N</i>-oxides and 2-heteroaryl-3,3-dimethylacrylonitriles.
Organic & biomolecular chemistry, 2021, 19, 8988-8998
7158334 CIFC21 H18 N4 O SP 1 21/n 112.1703; 8.7069; 17.7917
90; 104.923; 90
1821.72Kutasevich, Anton V.; Niktarov, Anton S.; Uvarova, Ekaterina S.; Karnoukhova, Valentina A.; Mityanov, Vitaly S.
A novel approach to bis(1,3-azol-2-yl)acetonitriles and bis(1,3-azol-2-yl)methanes <i>via</i> the [3 + 2]-dipolar cycloaddition of imidazole <i>N</i>-oxides and 2-heteroaryl-3,3-dimethylacrylonitriles.
Organic & biomolecular chemistry, 2021, 19, 8988-8998
7158335 CIFC11 H9 I O4 SP 1 21/c 111.705; 15.007; 7.459
90; 105.239; 90
1264.2Lu, Ling-Hui; Ou, Guangchuan; Zhao, Xiongjie; Wang, Yufei; Chen, Xuelian; Liao, Wenjun; Li, Shundan; Wu, Chao
Selective difunctionalization of electron-deficient alkynes: access to (<i>E</i>)-2-iodo-3-(methylthio)acrylate.
Organic & biomolecular chemistry, 2021, 19, 8128-8132
7158336 CIFC27 H26 Br2 N2 O4 SP 21 21 218.9489; 10.214; 29.3155
90; 90; 90
2679.56Yang, Xiao-Peng; Lv, Hao-Peng; Yang, Hao-Di; Wang, Bai-Lin; Wang, Xing-Wang
Box-copper catalyzed cascade asymmetric amidation for chiral <i>exo</i>-methylene aminoindoline derivatives.
Organic & biomolecular chemistry, 2021, 19, 9373-9378
7158337 CIFC16 H17 Cl3 N6 O2P 1 21/n 18.1174; 18.2984; 12.9072
90; 101.79; 90
1876.7Eltyshev, Alexander K.; Agafonova, Irina A.; Minin, Artem S.; Pozdina, Varvara A.; Shevirin, Vadim A.; Slepukhin, Pavel A.; Benassi, Enrico; Belskaya, Nataliya P.
Photophysics, photochemistry and bioimaging application of 8-azapurine derivatives.
Organic & biomolecular chemistry, 2021, 19, 9880-9896
7158338 CIFC16 H15 Cl3 N6 O2P -17.9266; 8.4539; 15.2045
86.573; 89.013; 65.02
921.87Eltyshev, Alexander K.; Agafonova, Irina A.; Minin, Artem S.; Pozdina, Varvara A.; Shevirin, Vadim A.; Slepukhin, Pavel A.; Benassi, Enrico; Belskaya, Nataliya P.
Photophysics, photochemistry and bioimaging application of 8-azapurine derivatives.
Organic & biomolecular chemistry, 2021, 19, 9880-9896
7158339 CIFC30 H19 N OP -17.4594; 11.112; 12.7546
72.929; 85.141; 80.711
996.6Rao, Maddali L. N.; Islam, Sk Shamim
Copper-catalyzed synthesis of 1-(2-benzofuryl)-N-heteroarenes from <i>o</i>-hydroxy-<i>gem</i>-(dibromovinyl)benzenes and N-heteroarenes.
Organic & biomolecular chemistry, 2021, 19, 9076-9080
7158340 CIFC21 H14 F3 N3 O7C 1 2/c 118.8139; 13.3867; 15.4997
90; 100.572; 90
3837.4Petropavlovskikh, Dmitry A.; Vorobyeva, Daria V.; Godovikov, Ivan A.; Nefedov, Sergey E.; Filippov, Oleg A.; Osipov, Sergey N.
Lossen rearrangement by Rh(III)-catalyzed C-H activation/annulation of aryl hydroxamates with alkynes: access to quinolone-containing amino acid derivatives.
Organic & biomolecular chemistry, 2021, 19, 9421-9426
7158341 CIFC27 H21 F3 N2 O5P b c a15.718; 13.4294; 24.95
90; 90; 90
5266.5Petropavlovskikh, Dmitry A.; Vorobyeva, Daria V.; Godovikov, Ivan A.; Nefedov, Sergey E.; Filippov, Oleg A.; Osipov, Sergey N.
Lossen rearrangement by Rh(III)-catalyzed C-H activation/annulation of aryl hydroxamates with alkynes: access to quinolone-containing amino acid derivatives.
Organic & biomolecular chemistry, 2021, 19, 9421-9426
7158342 CIFC58 H49 Cl4 F6 N4 O10P 1 21/c 110.8152; 16.2213; 32.017
90; 93.774; 90
5604.8Petropavlovskikh, Dmitry A.; Vorobyeva, Daria V.; Godovikov, Ivan A.; Nefedov, Sergey E.; Filippov, Oleg A.; Osipov, Sergey N.
Lossen rearrangement by Rh(III)-catalyzed C-H activation/annulation of aryl hydroxamates with alkynes: access to quinolone-containing amino acid derivatives.
Organic & biomolecular chemistry, 2021, 19, 9421-9426
7158343 CIFC30 H28 N2 O3P -19.1811; 9.9659; 14.9148
85.493; 80.059; 63.776
1205.83Liu, Chao; Zhao, Ruiqi; Song, Liangliang; Li, Zhenghua; Tian, Guilong; He, Yi; Van Meervelt, Luc; Peshkov, Vsevolod A.; Van der Eycken, Erik V.
Palladium-catalyzed post-Ugi arylative dearomatization/Michael addition cascade towards plicamine analogues.
Organic & biomolecular chemistry, 2021, 19, 9752-9757
7158344 CIFC24 H20 Br2 N6P 1 21/c 113.4998; 21.9675; 7.6004
90; 101.456; 90
2209.05Gupta, Shiv Shankar; Manisha, ?; Kumar, Rakesh; Dhiman, Ankit Kumar; Sharma, Upendra
Predictable site-selective functionalization: Promoter group assisted <i>para</i>-halogenation of <i>N</i>-substituted <b>(</b>hetero<b>)</b>aromatics under metal-free condition.
Organic & biomolecular chemistry, 2021, 19, 9675-9687
7158345 CIFC23 H26 N4 OP 1 21/c 115.2432; 6.8557; 19.6543
90; 99.415; 90
2026.3Soam, Pooja; Gaba, Hashmita; Mandal, Debasish; Tyagi, Vikas
A Pd-catalyzed one-pot cascade consisting of C-C/C-O/N-N bond formation to access benzoxazine fused 1,2,3-triazoles.
Organic & biomolecular chemistry, 2021, 19, 9936-9945
7158346 CIFC20 H13 N3P 21 21 219.2668; 10.713; 7.8156
90; 90; 90
1613.18Jia, Ruo-Ling; Liu, Qing-Ling; Yang, Long-Wei; Deng, Shi; Song, Yang
[6 + 3] Annulations of Morita-Baylis-Hillman carbonates and dicyanoheptafulvene.
Organic & biomolecular chemistry, 2021, 19, 9867-9871
7158347 CIFC17 H14 N2 O2P b c a11.631; 14.557; 15.796
90; 90; 90
2674.5Xu, Zhaoliang; Hu, Yu; Wang, Lei; Sun, Mingli; Li, Pinhua
Merging cobalt and photoredox catalysis for the C8-H alkoxylation of 1-naphthylamine derivatives with alcohols.
Organic & biomolecular chemistry, 2021, 19, 10112-10119
7158348 CIFC33 H29 N O7P -110.646; 11.634; 12.087
101.823; 109.747; 91.715
1371.1Soares, Maria I. L.; Gomes, Clara S. B.; Oliveira, M Conceição; Marçalo, Joaquim; Pinho E Melo, Teresa M V D
Synthesis of 5<i>H</i>-chromeno[3,4-<i>b</i>]pyridines <i>via</i> DABCO-catalyzed [3 + 3] annulation of 3-nitro-2<i>H</i>-chromenes and allenoates.
Organic & biomolecular chemistry, 2021, 19, 9711-9722
7158349 CIFC22 H19 N O6P -18.708; 13.624; 17.004
66.753; 79.781; 88.762
1821.5Soares, Maria I. L.; Gomes, Clara S. B.; Oliveira, M Conceição; Marçalo, Joaquim; Pinho E Melo, Teresa M V D
Synthesis of 5<i>H</i>-chromeno[3,4-<i>b</i>]pyridines <i>via</i> DABCO-catalyzed [3 + 3] annulation of 3-nitro-2<i>H</i>-chromenes and allenoates.
Organic & biomolecular chemistry, 2021, 19, 9711-9722
7158350 CIFC11 H9 F3 N2 O SP b c a8.3925; 11.705; 23.1584
90; 90; 90
2274.9Thomas Passia, Marco; Schöbel, Jan-Hendrik; Julian Lentelink, Niklas; Truong, Khai-Nghi; Rissanen, Kari; Bolm, Carsten
Synthesis of trifluoromethyl-substituted 1,2,6-thiadiazine 1-oxides from sulfonimidamides under mechanochemical conditions.
Organic & biomolecular chemistry, 2021, 19, 9470-9475
7158351 CIFC11 H8 Br F3 N2 O SP -17.6104; 7.8056; 12.0015
90.867; 102.061; 115.696
623.71Thomas Passia, Marco; Schöbel, Jan-Hendrik; Julian Lentelink, Niklas; Truong, Khai-Nghi; Rissanen, Kari; Bolm, Carsten
Synthesis of trifluoromethyl-substituted 1,2,6-thiadiazine 1-oxides from sulfonimidamides under mechanochemical conditions.
Organic & biomolecular chemistry, 2021, 19, 9470-9475
7158352 CIFC18 H23 N3 O3P 1 21/c 113.6962; 13.6338; 9.271
90; 104.983; 90
1672.33McNaughton, Daniel A.; To, Tsz Ying Teresa; Hawkins, Bryson A.; Hibbs, David E.; Gale, Philip A.
Delivering anion transporters to lipid bilayers in water.
Organic & biomolecular chemistry, 2021, 19, 9624-9628
7158353 CIFC34 H59 Cl N4 O3P -18.1181; 13.6649; 17.6062
108.557; 100.746; 95.887
1791.4McNaughton, Daniel A.; To, Tsz Ying Teresa; Hawkins, Bryson A.; Hibbs, David E.; Gale, Philip A.
Delivering anion transporters to lipid bilayers in water.
Organic & biomolecular chemistry, 2021, 19, 9624-9628
7158354 CIFC21 H23 N3 O4C 1 2/c 142.9415; 6.2417; 13.2277
90; 94.68; 90
3533.57McNaughton, Daniel A.; To, Tsz Ying Teresa; Hawkins, Bryson A.; Hibbs, David E.; Gale, Philip A.
Delivering anion transporters to lipid bilayers in water.
Organic & biomolecular chemistry, 2021, 19, 9624-9628
7158355 CIFC20 H25 N O5P 1 21/c 113.5595; 7.5471; 18.0224
90; 106; 90
1772.87Efremova, Mariia M.; Makarova, Anastasia A.; Novikov, Alexander S.; Kryukova, Mariya A.; Kuznetsov, Mikhail A.; Molchanov, Alexander P.
Regio- and stereoselective (3 + 2)-cycloaddition reactions of nitrones with cyclic allenes.
Organic & biomolecular chemistry, 2021, 19, 9773-9784
7158356 CIFC22 H25 Cl2 N O6P 1 21/n 113.0854; 7.50448; 22.3639
90; 92.532; 90
2193.97Efremova, Mariia M.; Makarova, Anastasia A.; Novikov, Alexander S.; Kryukova, Mariya A.; Kuznetsov, Mikhail A.; Molchanov, Alexander P.
Regio- and stereoselective (3 + 2)-cycloaddition reactions of nitrones with cyclic allenes.
Organic & biomolecular chemistry, 2021, 19, 9773-9784
7158357 CIFC20 H23 N O5P 21 21 218.3206; 10.3874; 20.7185
90; 90; 90
1790.69Efremova, Mariia M.; Makarova, Anastasia A.; Novikov, Alexander S.; Kryukova, Mariya A.; Kuznetsov, Mikhail A.; Molchanov, Alexander P.
Regio- and stereoselective (3 + 2)-cycloaddition reactions of nitrones with cyclic allenes.
Organic & biomolecular chemistry, 2021, 19, 9773-9784
7158358 CIFC22 H25 Cl2 N O6P 1 21/n 18.9201; 27.3837; 9.5899
90; 109.369; 90
2209.9Efremova, Mariia M.; Makarova, Anastasia A.; Novikov, Alexander S.; Kryukova, Mariya A.; Kuznetsov, Mikhail A.; Molchanov, Alexander P.
Regio- and stereoselective (3 + 2)-cycloaddition reactions of nitrones with cyclic allenes.
Organic & biomolecular chemistry, 2021, 19, 9773-9784
7158359 CIFC40 H50 O13P 41 21 210.2285; 10.2285; 31.7311
90; 90; 90
3319.78Liu, Shuai; Zhang, Cui-Shan; Ran, Xiao-Qian; Tang, Xiao-Han; Guo, Ya-Rong; Yan, Ying; Yao, Yong-Gang; Hao, Xiao-Jiang; Luo, Rong-Can; Di, Ying-Tong
Perforalactones D and E, two new C-20 quassinoids with potential activity to induce lysosomal biogenesis from the twigs of <i>Harrisonia perforata</i> (Blanco) Merr.
Organic & biomolecular chemistry, 2021, 19, 9637-9640
7158360 CIFC31 H23 Br N2 O5 SP 1 21/c 110.957; 29.1941; 8.9667
90; 101.076; 90
2814.84Zheng, Yi; Zhang, Ting-Ting; Shen, Wen-Bo
Gold-catalyzed oxidative cyclization of amide-alkynes: access to functionalized γ-lactams.
Organic & biomolecular chemistry, 2021, 19, 9688-9691
7158361 CIFC26 H30 O4P -110.5525; 10.5881; 11.4412
102.568; 105.923; 105.637
1123.59Xiao, Jian; Zhao, Jun; Wang, Ya-Wen; Luo, Gan; Peng, Yu
Total syntheses of (+)-adunctins C and D: assignment of their absolute configurations.
Organic & biomolecular chemistry, 2021, 19, 9840-9843
7158362 CIFC26 H28 O4I 1 2/a 120.8005; 5.76195; 37.1847
90; 98.257; 90
4410.4Xiao, Jian; Zhao, Jun; Wang, Ya-Wen; Luo, Gan; Peng, Yu
Total syntheses of (+)-adunctins C and D: assignment of their absolute configurations.
Organic & biomolecular chemistry, 2021, 19, 9840-9843
7158363 CIFC26 H30 O4P 110.6249; 10.6722; 11.3614
105.317; 102.94; 105.98
1131.72Xiao, Jian; Zhao, Jun; Wang, Ya-Wen; Luo, Gan; Peng, Yu
Total syntheses of (+)-adunctins C and D: assignment of their absolute configurations.
Organic & biomolecular chemistry, 2021, 19, 9840-9843
7158364 CIFC26 H38 Cl N3 O5C 1 2/c 117.4753; 11.4632; 26.206
90; 99.65; 90
5175.4Xu, Zan-Xin; Li, Bin; Tian, Ying; Li, Min; Dong, Jun-Xing; Zhang, Guang-Jie
Pentacyclic spermidine alkaloids with radioprotective and anti-inflammatory activities from <i>Orychophragmus violaceus</i>.
Organic & biomolecular chemistry, 2021, 19, 9844-9848
7158365 CIFC46 H26P 1 21/n 19.8457; 19.1932; 17.0462
90; 101.212; 90
3159.7Islam, Khadimul; Narjinari, Himani; Bisarya, Akshara; Kumar, Akshai
Multi-fold Sonogashira coupling: a new and convenient approach to obtain tetraalkynyl anthracenes with tunable photophysical properties.
Organic & biomolecular chemistry, 2021, 19, 9692-9704
7158366 CIFC34 H42 Si4P -16.0741; 11.2759; 14.146
99.128; 96.304; 105.017
912.3Islam, Khadimul; Narjinari, Himani; Bisarya, Akshara; Kumar, Akshai
Multi-fold Sonogashira coupling: a new and convenient approach to obtain tetraalkynyl anthracenes with tunable photophysical properties.
Organic & biomolecular chemistry, 2021, 19, 9692-9704
7158367 CIFC50 H34 O4P -14.6663; 14; 14.5094
75.898; 83.094; 83.357
908.96Islam, Khadimul; Narjinari, Himani; Bisarya, Akshara; Kumar, Akshai
Multi-fold Sonogashira coupling: a new and convenient approach to obtain tetraalkynyl anthracenes with tunable photophysical properties.
Organic & biomolecular chemistry, 2021, 19, 9692-9704
7158368 CIFC54 H46 N4P -19.2771; 9.6139; 14.3349
71.119; 86.812; 61.782
1058.66Islam, Khadimul; Narjinari, Himani; Bisarya, Akshara; Kumar, Akshai
Multi-fold Sonogashira coupling: a new and convenient approach to obtain tetraalkynyl anthracenes with tunable photophysical properties.
Organic & biomolecular chemistry, 2021, 19, 9692-9704
7158369 CIFC32 H18P 1 21/n 111.162; 11.978; 15.916
90; 90; 90
2127.9Islam, Khadimul; Narjinari, Himani; Bisarya, Akshara; Kumar, Akshai
Multi-fold Sonogashira coupling: a new and convenient approach to obtain tetraalkynyl anthracenes with tunable photophysical properties.
Organic & biomolecular chemistry, 2021, 19, 9692-9704
7158370 CIFC50 H34P 1 c 114.929; 11.922; 10.529
90; 92.393; 90
1872.4Islam, Khadimul; Narjinari, Himani; Bisarya, Akshara; Kumar, Akshai
Multi-fold Sonogashira coupling: a new and convenient approach to obtain tetraalkynyl anthracenes with tunable photophysical properties.
Organic & biomolecular chemistry, 2021, 19, 9692-9704
7158371 CIFC22 H13 F3 O2P 1 21/c 114.104; 15.1682; 24.3684
90; 102.661; 90
5086.4Zeng, Piaopiao; Huang, Xiaoxiao; Tang, Wei; Chen, Zhiwei
Copper-catalyzed cascade radical cyclization of alkynoates: construction of aryldifluoromethylated coumarins.
Organic & biomolecular chemistry, 2021, 19, 10223-10227
7158373 CIFC15 H14 Br N O4P 1 21/c 16.70863; 31.0104; 6.93722
90; 110.2; 90
1354.44Milyutin, Constantine V.; Galimova, Renata D.; Komogortsev, Andrey N.; Lichitskii, Boris V.; Melekhina, Valeriya G.; Migulin, Vasily A.; Fakhrutdinov, Artem N.; Minyaev, Mikhail E.
Photoinduced assembly of the 3,4,4a,7a-tetrahydro-1<i>H</i>-cyclopenta[<i>b</i>]pyridine-2,7-dione core on the basis of allomaltol derivatives.
Organic & biomolecular chemistry, 2021, 19, 9975-9985
7158374 CIFC19 H27 N3 O6P 1 21/n 19.2023; 10.58; 20.2538
90; 101.586; 90
1931.74Milyutin, Constantine V.; Galimova, Renata D.; Komogortsev, Andrey N.; Lichitskii, Boris V.; Melekhina, Valeriya G.; Migulin, Vasily A.; Fakhrutdinov, Artem N.; Minyaev, Mikhail E.
Photoinduced assembly of the 3,4,4a,7a-tetrahydro-1<i>H</i>-cyclopenta[<i>b</i>]pyridine-2,7-dione core on the basis of allomaltol derivatives.
Organic & biomolecular chemistry, 2021, 19, 9975-9985
7158375 CIFC34 H32 N2 O4 SP 1 21/c 19.7637; 28.138; 10.943
90; 104.379; 90
2912.2Zhang, Dongxin; Cheng, Qihang; Chen, Lvjia; Deng, Huiqing; Cai, Hu; Zhang, Qian-Feng
Lewis acid-catalyzed [3 + 2] annulations of oxindole based spirocyclic donor-acceptor cyclopropanes with ynamides.
Organic & biomolecular chemistry, 2021, 19, 9645-9648
7158376 CIFC8 H11 N5 O3 SP 1 21/c 18.7388; 8.7377; 15.3935
90; 105.809; 90
1130.94Fuller, Rebecca O.; Taylor, Madeleine R.; Duggin, Margot; Bissember, Alex C.; Canty, Allan J.; Judd, Martyna M.; Cox, Nicholas; Moggach, Stephen A.; Turner, Gemma F.
Enhanced synthesis of oxo-verdazyl radicals bearing sterically-and electronically-diverse C3-substituents.
Organic & biomolecular chemistry, 2021, 19, 10120-10138
7158377 CIFC19 H22 N4 OP -17.5838; 9.8117; 12.8968
102.553; 92.841; 111.32
863.837Fuller, Rebecca O.; Taylor, Madeleine R.; Duggin, Margot; Bissember, Alex C.; Canty, Allan J.; Judd, Martyna M.; Cox, Nicholas; Moggach, Stephen A.; Turner, Gemma F.
Enhanced synthesis of oxo-verdazyl radicals bearing sterically-and electronically-diverse C3-substituents.
Organic & biomolecular chemistry, 2021, 19, 10120-10138
7158378 CIFC19 H22 N4 O3P b c a10.9788; 14.7369; 22.0879
90; 90; 90
3573.68Fuller, Rebecca O.; Taylor, Madeleine R.; Duggin, Margot; Bissember, Alex C.; Canty, Allan J.; Judd, Martyna M.; Cox, Nicholas; Moggach, Stephen A.; Turner, Gemma F.
Enhanced synthesis of oxo-verdazyl radicals bearing sterically-and electronically-diverse C3-substituents.
Organic & biomolecular chemistry, 2021, 19, 10120-10138
7158379 CIFC13 H14 N4 O S2C 1 2/c 17.3232; 19.6029; 10.4905
90; 107.845; 90
1433.52Fuller, Rebecca O.; Taylor, Madeleine R.; Duggin, Margot; Bissember, Alex C.; Canty, Allan J.; Judd, Martyna M.; Cox, Nicholas; Moggach, Stephen A.; Turner, Gemma F.
Enhanced synthesis of oxo-verdazyl radicals bearing sterically-and electronically-diverse C3-substituents.
Organic & biomolecular chemistry, 2021, 19, 10120-10138
7158380 CIFC19 H22 N4 O3P -18.5045; 9.797; 11.9453
108.084; 100.023; 101.754
895.65Fuller, Rebecca O.; Taylor, Madeleine R.; Duggin, Margot; Bissember, Alex C.; Canty, Allan J.; Judd, Martyna M.; Cox, Nicholas; Moggach, Stephen A.; Turner, Gemma F.
Enhanced synthesis of oxo-verdazyl radicals bearing sterically-and electronically-diverse C3-substituents.
Organic & biomolecular chemistry, 2021, 19, 10120-10138
7158381 CIFC9 H13 N5 OC 1 2/c 119.7981; 7.6021; 16.1604
90; 124.601; 90
2002.05Fuller, Rebecca O.; Taylor, Madeleine R.; Duggin, Margot; Bissember, Alex C.; Canty, Allan J.; Judd, Martyna M.; Cox, Nicholas; Moggach, Stephen A.; Turner, Gemma F.
Enhanced synthesis of oxo-verdazyl radicals bearing sterically-and electronically-diverse C3-substituents.
Organic & biomolecular chemistry, 2021, 19, 10120-10138
7158382 CIFC20 H22 N4 O2 SP n m a4.931; 19.1334; 20.4301
90; 90; 90
1927.51Fuller, Rebecca O.; Taylor, Madeleine R.; Duggin, Margot; Bissember, Alex C.; Canty, Allan J.; Judd, Martyna M.; Cox, Nicholas; Moggach, Stephen A.; Turner, Gemma F.
Enhanced synthesis of oxo-verdazyl radicals bearing sterically-and electronically-diverse C3-substituents.
Organic & biomolecular chemistry, 2021, 19, 10120-10138
7158383 CIFC25 H22 N4 O S2C 1 2/c 118.9089; 11.613; 10.5619
90; 90.812; 90
2319.04Fuller, Rebecca O.; Taylor, Madeleine R.; Duggin, Margot; Bissember, Alex C.; Canty, Allan J.; Judd, Martyna M.; Cox, Nicholas; Moggach, Stephen A.; Turner, Gemma F.
Enhanced synthesis of oxo-verdazyl radicals bearing sterically-and electronically-diverse C3-substituents.
Organic & biomolecular chemistry, 2021, 19, 10120-10138
7158384 CIFC15 H16 N6 OP 1 21/c 111.4529; 10.4903; 12.3136
90; 98.94; 90
1461.44Fuller, Rebecca O.; Taylor, Madeleine R.; Duggin, Margot; Bissember, Alex C.; Canty, Allan J.; Judd, Martyna M.; Cox, Nicholas; Moggach, Stephen A.; Turner, Gemma F.
Enhanced synthesis of oxo-verdazyl radicals bearing sterically-and electronically-diverse C3-substituents.
Organic & biomolecular chemistry, 2021, 19, 10120-10138
7158385 CIFC22 H20 Cl N3 O4P 1 21 17.7803; 9.3559; 14.8204
90; 90.009; 90
1078.8Kaur, Banni Preet; Sharma, Vivek; Sahoo, Subash Chandra; Chimni, Swapandeep Singh
Low catalyst loading enabled organocatalytic synthesis of chiral bis-heterocyclic frameworks containing pyrazole and isoxazole.
Organic & biomolecular chemistry, 2021, 19, 9910-9924
7158386 CIFC12 H17 F3 N2 O2P 21 21 215.5102; 9.087; 25.588
90; 90; 90
1281.2Goryaeva, Marina V.; Kushch, Svetlana O.; Burgart, Yanina V.; Ezhikova, Marina A.; Kodess, Mikhail I.; Slepukhin, Pavel A.; Triandafilova, Galina A.; Krasnykh, Olga P.; Yakovleva, Ekaterina I.; Zarubaev, Vladimir V.; Sinegubova, Ekaterina O.; Esaulkova, Iana L.; Shtro, Anna A.; Galochkina, Anastasia V.; Nikolaeva, Yulia V.; Saloutin, Victor I.
New heteroanalogs of tricyclic ascidian alkaloids: synthesis and biological activity.
Organic & biomolecular chemistry, 2021, 19, 9925-9935
7158387 CIFC12 H16 F3 N O3P -15.6852; 9.4367; 12.6134
77.963; 77.679; 76.073
632.8Goryaeva, Marina V.; Kushch, Svetlana O.; Burgart, Yanina V.; Ezhikova, Marina A.; Kodess, Mikhail I.; Slepukhin, Pavel A.; Triandafilova, Galina A.; Krasnykh, Olga P.; Yakovleva, Ekaterina I.; Zarubaev, Vladimir V.; Sinegubova, Ekaterina O.; Esaulkova, Iana L.; Shtro, Anna A.; Galochkina, Anastasia V.; Nikolaeva, Yulia V.; Saloutin, Victor I.
New heteroanalogs of tricyclic ascidian alkaloids: synthesis and biological activity.
Organic & biomolecular chemistry, 2021, 19, 9925-9935
7158388 CIFC13 H19 F3 N2 O2P 1 21/c 16.6874; 17.3402; 11.9242
90; 96.885; 90
1372.8Goryaeva, Marina V.; Kushch, Svetlana O.; Burgart, Yanina V.; Ezhikova, Marina A.; Kodess, Mikhail I.; Slepukhin, Pavel A.; Triandafilova, Galina A.; Krasnykh, Olga P.; Yakovleva, Ekaterina I.; Zarubaev, Vladimir V.; Sinegubova, Ekaterina O.; Esaulkova, Iana L.; Shtro, Anna A.; Galochkina, Anastasia V.; Nikolaeva, Yulia V.; Saloutin, Victor I.
New heteroanalogs of tricyclic ascidian alkaloids: synthesis and biological activity.
Organic & biomolecular chemistry, 2021, 19, 9925-9935
7158389 CIFC13 H20 F3 N O4P 1 21/c 113.671; 5.8015; 18.074
90; 93.43; 90
1430.9Goryaeva, Marina V.; Kushch, Svetlana O.; Burgart, Yanina V.; Ezhikova, Marina A.; Kodess, Mikhail I.; Slepukhin, Pavel A.; Triandafilova, Galina A.; Krasnykh, Olga P.; Yakovleva, Ekaterina I.; Zarubaev, Vladimir V.; Sinegubova, Ekaterina O.; Esaulkova, Iana L.; Shtro, Anna A.; Galochkina, Anastasia V.; Nikolaeva, Yulia V.; Saloutin, Victor I.
New heteroanalogs of tricyclic ascidian alkaloids: synthesis and biological activity.
Organic & biomolecular chemistry, 2021, 19, 9925-9935
7158390 CIFC11 H14 F3 N O3P -15.4368; 8.606; 12.6785
93.198; 100.084; 92.872
582.06Goryaeva, Marina V.; Kushch, Svetlana O.; Burgart, Yanina V.; Ezhikova, Marina A.; Kodess, Mikhail I.; Slepukhin, Pavel A.; Triandafilova, Galina A.; Krasnykh, Olga P.; Yakovleva, Ekaterina I.; Zarubaev, Vladimir V.; Sinegubova, Ekaterina O.; Esaulkova, Iana L.; Shtro, Anna A.; Galochkina, Anastasia V.; Nikolaeva, Yulia V.; Saloutin, Victor I.
New heteroanalogs of tricyclic ascidian alkaloids: synthesis and biological activity.
Organic & biomolecular chemistry, 2021, 19, 9925-9935
7158391 CIFC17 H19 F3 N2 O2P -111.7168; 11.9298; 12.1371
70.519; 89.748; 79.574
1570.1Goryaeva, Marina V.; Kushch, Svetlana O.; Burgart, Yanina V.; Ezhikova, Marina A.; Kodess, Mikhail I.; Slepukhin, Pavel A.; Triandafilova, Galina A.; Krasnykh, Olga P.; Yakovleva, Ekaterina I.; Zarubaev, Vladimir V.; Sinegubova, Ekaterina O.; Esaulkova, Iana L.; Shtro, Anna A.; Galochkina, Anastasia V.; Nikolaeva, Yulia V.; Saloutin, Victor I.
New heteroanalogs of tricyclic ascidian alkaloids: synthesis and biological activity.
Organic & biomolecular chemistry, 2021, 19, 9925-9935
7158392 CIFC12 H16 F3 N O3C 1 2/c 117.7173; 5.9455; 24.594
90; 101.644; 90
2537.4Goryaeva, Marina V.; Kushch, Svetlana O.; Burgart, Yanina V.; Ezhikova, Marina A.; Kodess, Mikhail I.; Slepukhin, Pavel A.; Triandafilova, Galina A.; Krasnykh, Olga P.; Yakovleva, Ekaterina I.; Zarubaev, Vladimir V.; Sinegubova, Ekaterina O.; Esaulkova, Iana L.; Shtro, Anna A.; Galochkina, Anastasia V.; Nikolaeva, Yulia V.; Saloutin, Victor I.
New heteroanalogs of tricyclic ascidian alkaloids: synthesis and biological activity.
Organic & biomolecular chemistry, 2021, 19, 9925-9935
7158393 CIFC12 H17 F3 N2 O2P b c a12.8729; 12.6636; 15.6817
90; 90; 90
2556.4Goryaeva, Marina V.; Kushch, Svetlana O.; Burgart, Yanina V.; Ezhikova, Marina A.; Kodess, Mikhail I.; Slepukhin, Pavel A.; Triandafilova, Galina A.; Krasnykh, Olga P.; Yakovleva, Ekaterina I.; Zarubaev, Vladimir V.; Sinegubova, Ekaterina O.; Esaulkova, Iana L.; Shtro, Anna A.; Galochkina, Anastasia V.; Nikolaeva, Yulia V.; Saloutin, Victor I.
New heteroanalogs of tricyclic ascidian alkaloids: synthesis and biological activity.
Organic & biomolecular chemistry, 2021, 19, 9925-9935
7158394 CIFC19 H22 F3 N3 O2P 1 21/c 110.2653; 9.7195; 19.2671
90; 104.837; 90
1858.3Goryaeva, Marina V.; Kushch, Svetlana O.; Burgart, Yanina V.; Ezhikova, Marina A.; Kodess, Mikhail I.; Slepukhin, Pavel A.; Triandafilova, Galina A.; Krasnykh, Olga P.; Yakovleva, Ekaterina I.; Zarubaev, Vladimir V.; Sinegubova, Ekaterina O.; Esaulkova, Iana L.; Shtro, Anna A.; Galochkina, Anastasia V.; Nikolaeva, Yulia V.; Saloutin, Victor I.
New heteroanalogs of tricyclic ascidian alkaloids: synthesis and biological activity.
Organic & biomolecular chemistry, 2021, 19, 9925-9935

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