中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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; Song, GQ; Bai, DL
刊名TETRAHEDRON
出版日期1999-12-03
卷号55期号:49页码:13999-14004
ISSN号0040-4020
DOI10.1016/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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