Highly Regio- and Stereoselective Synthesis of Tetrasubstituted Olefins by the Three-Component Tandem Reaction of Allylzinc Bromide, Acetylenic Sulfone, and Halohydrocarbon-Reference-Cited by-同舟云学术

Highly Regio- and Stereoselective Synthesis of Tetrasubstituted Olefins by the Three-Component Tandem Reaction of Allylzinc Bromide, Acetylenic Sulfone, and Halohydrocarbon

Published:2006-01-13 Issue:3 Volume:8 Page:431-434
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Xie Meihua¹,Wang Jialiang¹,Gu Xiaoxia¹,Sun Ying¹,Wang Shaowu¹

Affiliation:

1. Anhui Key Laboratory of Functional Molecular Solids, Institute of Organic Chemistry, School of Chemistry and Materials Science, Anhui Normal University, Wuhu, Anhui 241000, China, and State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol052640i

Reference17 articles.

1. Stereoselective Synthesis of Highly Functionalized Trisubstituted Olefins via the Aldol Reaction of Allenoxyborinates with Carbonyl Compounds

2. New Nickel-Catalyzed Carbozincation of Alkynes: A Short Synthesis of(Z)-Tamoxifen

3. Desulfonylation reactions: Recent developments

4. The chemistry of acetylenic and allenic sulfones

5. Multiply convergent syntheses via conjugate-addition reactions to cycloalkenyl sulfones

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