Si-C-X and Si-C-EWG as Carbanion Equivalents under Lewis Base Activation (n?→?σ*)-Reference-Cited by-同舟云学术

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Si-C-X and Si-C-EWG as Carbanion Equivalents under Lewis Base Activation (n?→?σ*)

Published:2016-08-17 Issue: Volume: Page:903-966
ISSN:
Container-title:Lewis Base Catalysis in Organic Synthesis
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Author:

Fang Ping¹,Ding Chang-Hua²,Hou Xue-Long¹²

Affiliation:

1. Chinese Academy of Sciences; Shanghai Institute of Organic Chemistry, State Key Laboratory of Organometallic Chemistry; 345 Lingling Road Shanghai 200032 China

2. Chinese Academy of Sciences; Shanghai Institute of Organic Chemistry, Shanghai-Hong Kong Joint Laboratory in Chemical Synthesis; 345 Lingling Road Shanghai 200032 China

Publisher

Wiley-VCH Verlag GmbH & Co. KGaA

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/9783527675142.ch18/fullpdf

Reference284 articles.

1. Tetrahedron report number 234 Synthetic aspects of the use of organosilicon compounds under nucleophilic catalysis conditions

2. Perfluoroalkylation with Organosilicon Reagents

3. Recent Progress in Lewis Base Activation and Control of Stereoselectivity in the Additions of Trimethylsilyl Nucleophiles

4. Organotin Chemistry

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1. Novel synthesis of 2,3-dihydrobenzofuran-3-amines from salicylic aldehydes: Trimethylsilyl as traceless activating group;Tetrahedron Letters;2024-04

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