A General Strategy for Regiocontrol in Nickel-Catalyzed Reductive Couplings of Aldehydes and Alkynes-Reference-Cited by-同舟云学术

A General Strategy for Regiocontrol in Nickel-Catalyzed Reductive Couplings of Aldehydes and Alkynes

Published:2010-04-15 Issue:18 Volume:132 Page:6304-6305
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Malik Hasnain A.¹,Sormunen Grant J.¹,Montgomery John¹

Affiliation:

1. 930 North University Avenue, Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109-1055

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja102262v

Reference38 articles.

1. Nickel-Catalyzed Reductive Cyclizations and Couplings

2. bMontgomery, J. and Sormunen, G. J.InMetal Catalyzed Reductive C−C Bond Formation: A Departure from Preformed Organometallic Reagents; Krische, M. J., Ed.; Springer: Berlin, 2007; Vol.279, pp1−23.

3. Regioselectivity and enantioselectivity in nickel-catalysed reductive coupling reactions of alkynes

4. Enantiomerically Enriched Allylic Alcohols and Allylic Amines via C–C Bond-Forming Hydrogenation: Asymmetric Carbonyl and Imine Vinylation

5. Catalytic Carbonyl Addition through Transfer Hydrogenation: A Departure from Preformed Organometallic Reagents

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