Palladium-Catalyzed Diastereo- and Enantioselective Wagner−Meerwein Shift: Control of Absolute Stereochemistry in the C−C Bond Migration Event-Reference-Cited by-同舟云学术

Palladium-Catalyzed Diastereo- and Enantioselective Wagner−Meerwein Shift: Control of Absolute Stereochemistry in the C−C Bond Migration Event

Published:2008-04-23 Issue:19 Volume:130 Page:6231-6242
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Trost Barry M.¹,Xie Jia¹

Affiliation:

1. Department of Chemistry, Stanford University, Stanford, California 94305

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja7111299

Reference66 articles.

1. For an overview of Wagner–Meerwein shift and related reactions, see:Comprehensive Organic Synthesis, Vol. 3;Trost, B. M. and Fleming, I. Eds.; Pergamon Press: Oxford, 1991; Hanson, J. R., Chapter 3.1, pp 705–720; Rickborn, B., Chapter 3.2, pp 721–732 and Chapter 3.3, pp 733–776; Coveney, D. J., Chapter 3.4, pp 777–802.

2. A Catalytic Asymmetric Wagner−Meerwein Shift

3. Asymmetric Transition Metal-Catalyzed Allylic Alkylations

4. Pd Asymmetric Allylic Alkylation (AAA). A Powerful Synthetic Tool.

5. Molybdenum-Catalyzed Asymmetric Allylic Alkylations

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