Intramolecular CuCl-Mediated Oxidative Coupling of Alkenyltrimethylstannane Functions: An Effective Method for the Construction of Carbocyclic 1,3-Diene Systems-Reference-Cited by-同舟云学术

Intramolecular CuCl-Mediated Oxidative Coupling of Alkenyltrimethylstannane Functions: An Effective Method for the Construction of Carbocyclic 1,3-Diene Systems

Published:1996-01-01 Issue:5 Volume:118 Page:1215-1216
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Piers Edward¹,Romero Miguel A.¹

Affiliation:

1. Department of Chemistry, University of British Columbia, 2036 Main Mall, University Campus Vancouver, British Columbia, Canada V6T 1Z1

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja953648y

Reference11 articles.

1. The Palladium-Catalyzed Cross-Coupling Reactions of Organotin Reagents with Organic Electrophiles[New Synthetic Methods(58)]

2. Palladium-Catalysed Reactions of Organotin Compounds

3. PALLADIUM-CATALYZED COUPLING OF VINYL TRIFLATES WITH ORGANOSTANNANES: 4-tert-BUTYL-1-VINYLCYCLOHEXENE AND 1-(4-tert-BUTYLCYCLOHEXEN-1-YL)-2-PROPEN-1-ONE

4. Intramolecular palladium(0)-catalyzed coupling of enol triflate and vinylstannane functions. New annulation sequences leading to bicyclic diene systems

5. Annulations leading to diene systems. Total syntheses of the dolastane-type diterpenoids (±)-(5S,12R,14S)-dolasta-1(15),7,9-trien-14-ol and (±)-amijitrienol

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