The diastereoselectivity of electrophilic attack on trigonal carbon adjacent to a stereogenic centre: diastereoselective aldol reactions of open-chain enolates having a stereogenic centre carrying a silyl group at the ? position-Reference-Cited by-同舟云学术

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The diastereoselectivity of electrophilic attack on trigonal carbon adjacent to a stereogenic centre: diastereoselective aldol reactions of open-chain enolates having a stereogenic centre carrying a silyl group at the ? position

Published:1992 Issue:24 Volume: Page:3295
ISSN:0300-922X
Container-title:Journal of the Chemical Society, Perkin Transactions 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Fleming Ian,Kilburn Jeremy D.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1992/P1/P19920003295

Cited by 43 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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4. Direct Synthesis of Diverse β-Fluoroethylamines by a Multicomponent Protocol;Chemistry - A European Journal;2013-02-10

5. Enantioselective Synthesis of Deoxymannojirimycin Based on Sharpless Asymmetric Epoxidation of a Highly Functionalized Allylic Alcohol;European Journal of Organic Chemistry;2011-03-23

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