Spiro[pyrrolidine-2,3 '-oxindole] derivatives synthesized by novel regionselective 1,3-dipolar cycloadditions | |
Chen, Gang1,4; Yang, Jing2![]() ![]() ![]() | |
通讯作者 | Chen, G (reprint author), Chinese Acad Sci, State Key Lab Phytochem & Plant Resources W China, Kunming Inst Bot, Kunming 650204, Peoples R China. ; gangchen@xsyu.edu.cn |
2012-02-01 | |
发表期刊 | MOLECULAR DIVERSITY
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ISSN | 1381-1991 |
卷号 | 16期号:1页码:151-156 |
摘要 | A series of spiro-oxindole derivatives was synthesized by novel regioselective 1,3-dipolar cycloadditions of isatin, alpha-amino acids, and (E)-beta-aryl-nitro-olefins. Regioisomers were produced in each reaction and the major products showed different regioselectivity compared to previously reported spiro-oxindole derivatives. |
关键词 | Huisgen Reaction 1 Regioisomers 3-dipolar Cycloaddition Spiro Compounds Nitro Group |
学科领域 | Biochemistry & Molecular Biology ; Chemistry, Applied ; Chemistry, Medicinal ; Chemistry, Multidisciplinary |
DOI | 10.1007/s11030-011-9342-1 |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000305220000014 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://ir.kib.ac.cn/handle/151853/15101 |
专题 | 植物化学与西部植物资源持续利用国家重点实验室 |
作者单位 | 1.Chinese Acad Sci, State Key Lab Phytochem & Plant Resources W China, Kunming Inst Bot, Kunming 650204, Peoples R China 2.Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China 3.Chinese Acad Med Sci, Inst Mat Med, Beijing 100050, Peoples R China 4.Xian Shiyou Univ, Coll Chem & Chem Engn, Xian 710065, Shaanxi, Peoples R China |
推荐引用方式 GB/T 7714 | Chen, Gang,Yang, Jing,Gao, Suo,et al. Spiro[pyrrolidine-2,3 '-oxindole] derivatives synthesized by novel regionselective 1,3-dipolar cycloadditions[J]. MOLECULAR DIVERSITY,2012,16(1):151-156. |
APA | Chen, Gang.,Yang, Jing.,Gao, Suo.,He, Hongping.,Li, Shunlin.,...&Hao, Xiaojiang.(2012).Spiro[pyrrolidine-2,3 '-oxindole] derivatives synthesized by novel regionselective 1,3-dipolar cycloadditions.MOLECULAR DIVERSITY,16(1),151-156. |
MLA | Chen, Gang,et al."Spiro[pyrrolidine-2,3 '-oxindole] derivatives synthesized by novel regionselective 1,3-dipolar cycloadditions".MOLECULAR DIVERSITY 16.1(2012):151-156. |
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