Combined Directed ortho and Remote Metalation−Suzuki Cross-Coupling Strategies. Efficient Synthesis of Heteroaryl-Fused Benzopyranones from Biaryl O-Carbamates-Reference-Cited by-同舟云学术

Combined Directed ortho and Remote Metalation−Suzuki Cross-Coupling Strategies. Efficient Synthesis of Heteroaryl-Fused Benzopyranones from Biaryl O-Carbamates

Published:2009-05-14 Issue:11 Volume:74 Page:4094-4103
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

James Clint A.¹,Coelho Antonio Luiz¹,Gevaert Matt¹,Forgione Pat¹,Snieckus Victor¹

Affiliation:

1. Department of Chemistry, University of Waterloo, Waterloo, ON, Canada N2L 3G1

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo900146d

Reference132 articles.

1. Combined Directed Remote Metalation−Transition Metal Catalyzed Cross Coupling Strategies: The Total Synthesis of the Aglycones of the Gilvocarcins V, M, and E and Arnottin I

2. bAnctil, E. J.G.; Snieckus, V.InMetal-Catalyzed Cross-Coupling Reactions,2nded.de Meijere, A.; Diederich, F., Eds.Wiley-VCH:Weinheim, Germany, 2004; Vol. 1, pp761−813.

3. Palladium-Catalyzed Cross-Coupling Reactions in Total Synthesis

4. The directed ortho lithiation of O-aryl carbamates. An anionic equivalent of the Fries rearrangement

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