Enantioselective Conversion of Primary Alcohols to α-exo-Methylene γ-Butyrolactones via Iridium-Catalyzed C–C Bond-Forming Transfer Hydrogenation: 2-(Alkoxycarbonyl)allylation-Reference-Cited by-同舟云学术

Enantioselective Conversion of Primary Alcohols to α-exo-Methylene γ-Butyrolactones via Iridium-Catalyzed C–C Bond-Forming Transfer Hydrogenation: 2-(Alkoxycarbonyl)allylation

Published:2012-06-26 Issue:27 Volume:134 Page:11100-11103
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Montgomery T. Patrick¹,Hassan Abbas¹,Park Boyoung Y.¹,Krische Michael J.¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of Texas at Austin, Austin, Texas 78712, United States

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja303839h

Reference64 articles.

1. Synthesis and Biological Activity of ?-Methylene-?-butyrolactones

2. Synthesis of Odd-membered Rings by the Reaction of β-Carbonylallylsilane or its Derivative as a Carbon 1,3-Dipole

3. Lactones: Generic Inhibitors of Enzymes?

4. The Renaissance of α-Methylene-γ-butyrolactones: New Synthetic Approaches

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