Organocatalytic approach to 3,5,6-trisubstituted and 4,6-disubstituted tetrahydropyran-2-ones
Xu DH(徐旦华) ; Zhang YH(张奕华) ; Ma DW(马大为)
刊名Tetrahedron Lett.
2010
卷号51期号:29页码:3827-3829
ISSN号0040-4039
其他题名有机催化合成3,5,6-三取代及4,6-二取代四氢吡喃-2-酮
通讯作者张奕华 ; 马大为
英文摘要The diarylprolinol ether-catalyzed Michael addition and subsequent cyclization of ethyl 3-methyl-2-oxobut-3-enoate with aldehydes, and gamma-substituted beta,gamma-unsaturated-alpha-ketoesters with acetaldehyde, afforded the corresponding lactals, which were subjected to oxidation and stereocontrolled hydrogenation to provide 3,5,6-trisubstituted and 4,6-disubstituted tetrahydropyran-2-ones with excellent enantioselectivities. (C) 2010 Elsevier Ltd. All rights reserved.
学科主题有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1016/j.tetlet.2010.05.077
语种英语
WOS记录号WOS:000279864100033
公开日期2013-02-19
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/15639]  
专题上海有机化学研究所_生命有机化学国家重点实验室
推荐引用方式
GB/T 7714
Xu DH,Zhang YH,Ma DW. Organocatalytic approach to 3,5,6-trisubstituted and 4,6-disubstituted tetrahydropyran-2-ones[J]. Tetrahedron Lett.,2010,51(29):3827-3829.
APA 徐旦华,张奕华,&马大为.(2010).Organocatalytic approach to 3,5,6-trisubstituted and 4,6-disubstituted tetrahydropyran-2-ones.Tetrahedron Lett.,51(29),3827-3829.
MLA 徐旦华,et al."Organocatalytic approach to 3,5,6-trisubstituted and 4,6-disubstituted tetrahydropyran-2-ones".Tetrahedron Lett. 51.29(2010):3827-3829.
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