Highly Regioselective Synthesis of Trisubstituted Allenes via Lithiation of 1-Aryl-3-alkylpropadiene, Subsequent Transmetalation, and Pd-Catalyzed Negishi Coupling Reaction-Reference-Cited by-同舟云学术

Highly Regioselective Synthesis of Trisubstituted Allenes via Lithiation of 1-Aryl-3-alkylpropadiene, Subsequent Transmetalation, and Pd-Catalyzed Negishi Coupling Reaction

Published:2008-03-26 Issue:8 Volume:10 Page:1521-1523
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhao Jinbo¹,Liu Yu¹,Ma Shengming¹

Affiliation:

1. Shanghai Institutre of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, People's Republic of China, and Shanghai Key Laboratory of Green Chemistry and Chemical Process, Department of Chemistry, East China Normal University, 3663 North Zhongshan Road, Shanghai 200062, People's Republic of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol8001909

Reference23 articles.

1. Regio et stereochimie de la reduction de derives d'alcools propargyliques catalysee par un complexe de palladium (O)

2. Palladium-catalysed preparation of 1,2-dienes by selective hydrogenolysis of alk-2-ynyl carbonates with ammonium formate

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