Cuprous Chloride Accelerated Stille Reactions. A General and Effective Coupling System for Sterically Congested Substrates and for Enantioselective Synthesis-Reference-Cited by-同舟云学术

Cuprous Chloride Accelerated Stille Reactions. A General and Effective Coupling System for Sterically Congested Substrates and for Enantioselective Synthesis

Published:1999-08-01 Issue:33 Volume:121 Page:7600-7605
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Han Xiaojun¹,Stoltz Brian M.¹,Corey E. J.¹

Affiliation:

1. Contribution from the Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts, 02138

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja991500z

Reference31 articles.

1. Chelate control in the rhodium-catalysed homogeneous hydrogenation of chiral allylic and homoallylic alcohols

2. Directed Homogeneous Hydrogenation[New Synthetic Methods(65)]

3. Stereoselective Hydrogenation of Simple Ketones Catalyzed by Ruthenium(II) Complexes

4. Cram selectivity in the reaction of 2-phenylpropanal with alkyllithium reagents: Myth and reality

5. Stille coupling versus cine substitution. Electronic effects also influence coupling sterically hindered stannanes

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