Unique Regio- and Stereoselectivity in Pd-Catalyzed Chlorocarbonylation Reaction of 2-Phenylethynyl Selenides and 2-Alkylethynyl Selenides. Highly Stereoselective Synthesis of 2-Seleno-3-chloroacrylates-Reference-Cited by-同舟云学术

Unique Regio- and Stereoselectivity in Pd-Catalyzed Chlorocarbonylation Reaction of 2-Phenylethynyl Selenides and 2-Alkylethynyl Selenides. Highly Stereoselective Synthesis of 2-Seleno-3-chloroacrylates

Published:2000-09-01 Issue:20 Volume:65 Page:6561-6565
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Huang Xian¹,Sun Aiming¹

Affiliation:

1. Department of Chemistry, Zhejiang University, Xixi Campus, Hangzhou 310028, Peoples Republic of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0006977

Reference39 articles.

1. Carbonyl olefination reaction using silyl-substituted organometallic compounds

2. New ene and reverse ene reactions. Formation of methyl sulfinates in the reaction of fluoromethane-antimony pentafluoride in sulfur dioxide and loss of sulfur dioxide from the corresponding sulfinic acids

3. Stereoselective synthesis of tetrasubstituted .alpha.,.beta.-unsaturated esters

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