Diastereoselective intramolecular [4+3] cycloaddition: Synthesis of a versatile precursor for preparation of 5,7-fused ring compounds
文献类型:期刊论文
作者 | Ou, LG; Hu, YH![]() ![]() |
刊名 | TETRAHEDRON
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出版日期 | 1999-12-03 |
卷号 | 55期号:49页码:13999-14004 |
ISSN号 | 0040-4020 |
DOI | 10.1016/S0040-4020(99)00882-0 |
文献子类 | Article |
英文摘要 | Compound 8 which could be used as a versatile precursor for the synthesis of 5,7-membered fused ring containing natural products was synthesized via tandem Pummerer rearrangement and intramolecular [4+3] cycloaddition in moderate yield and with high diastereoselectivity. (C) 1999 Elsevier Science Ltd. All rights: reserved. |
WOS关键词 | ORGANOLITHIUM REAGENTS ; OXABICYCLIC ALKENES ; CATIONS |
WOS研究方向 | Chemistry |
语种 | 英语 |
WOS记录号 | WOS:000083695600012 |
出版者 | PERGAMON-ELSEVIER SCIENCE LTD |
源URL | [http://119.78.100.183/handle/2S10ELR8/274670] ![]() |
专题 | 院士及顾问专家 药物化学研究室 |
通讯作者 | Bai, DL |
作者单位 | Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 200031, Peoples R China |
推荐引用方式 GB/T 7714 | Ou, LG,Hu, YH,Song, GQ,et al. Diastereoselective intramolecular [4+3] cycloaddition: Synthesis of a versatile precursor for preparation of 5,7-fused ring compounds[J]. TETRAHEDRON,1999,55(49):13999-14004. |
APA | Ou, LG,Hu, YH,Song, GQ,&Bai, DL.(1999).Diastereoselective intramolecular [4+3] cycloaddition: Synthesis of a versatile precursor for preparation of 5,7-fused ring compounds.TETRAHEDRON,55(49),13999-14004. |
MLA | Ou, LG,et al."Diastereoselective intramolecular [4+3] cycloaddition: Synthesis of a versatile precursor for preparation of 5,7-fused ring compounds".TETRAHEDRON 55.49(1999):13999-14004. |
入库方式: OAI收割
来源:上海药物研究所
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