中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Reversal of predominant enantioselectivity in the asymmetric alkynylation reaction using sulfamide-amine alcohols

文献类型:期刊论文

作者Mao, Jincheng; Zhang, Zhanjin; Wan, Boshun; Wu, Fan; Lu, Shiwei
刊名catalysis communications
出版日期2006-08-01
卷号7期号:8页码:550-553
关键词reversal of stereochemistry enantioselective alkynylzinc addition L-proline propargylic alcohols aldehydes
产权排序1;1
通讯作者万伯顺
英文摘要the change of substituent in the backbone of l-proline-derived sulfamide-amine alcohol ligand 3 provides chiral propargylic alcohols with the opposite configurations in significant enantioselectivities in the asymmetric addition of phenylacetylene to aldehydes. meanwhile, the ligand 3 in combination with ti((opr)-pr-i)(4) could also afford the products with opposite absolute configuration in high yields. (c) 2006 elsevier b.v. all rights reserved.
WOS标题词science & technology ; physical sciences
类目[WOS]chemistry, physical
研究领域[WOS]chemistry
关键词[WOS]aromatic-aldehydes ; phenylacetylene addition ; diethylzinc ; ligands ; alkynylzinc ; catalysts ; ketones ; binol
收录类别SCI ; IC ; CCR
原文出处true
语种英语
WOS记录号WOS:000238799500008
公开日期2010-11-30
源URL[http://159.226.238.44/handle/321008/97239]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
作者单位Chinese Acad Sci, Dalian Inst Chem Phys, Grp 202, Dalian 116023, Peoples R China
推荐引用方式
GB/T 7714
Mao, Jincheng,Zhang, Zhanjin,Wan, Boshun,et al. Reversal of predominant enantioselectivity in the asymmetric alkynylation reaction using sulfamide-amine alcohols[J]. catalysis communications,2006,7(8):550-553.
APA Mao, Jincheng,Zhang, Zhanjin,Wan, Boshun,Wu, Fan,&Lu, Shiwei.(2006).Reversal of predominant enantioselectivity in the asymmetric alkynylation reaction using sulfamide-amine alcohols.catalysis communications,7(8),550-553.
MLA Mao, Jincheng,et al."Reversal of predominant enantioselectivity in the asymmetric alkynylation reaction using sulfamide-amine alcohols".catalysis communications 7.8(2006):550-553.

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来源:大连化学物理研究所

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