Mechanism and Origins of Regio- and Enantioselectivities in RhI-Catalyzed Hydrogenative Couplings of 1,3-Diynes and Activated Carbonyl Partners: Intervention of a Cumulene Intermediate-Reference-Cited by-同舟云学术

Mechanism and Origins of Regio- and Enantioselectivities in RhI-Catalyzed Hydrogenative Couplings of 1,3-Diynes and Activated Carbonyl Partners: Intervention of a Cumulene Intermediate

Published:2011-03-01 Issue:14 Volume:17 Page:4021-4029
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Liu Peng,Krische Michael J.,Houk Kendall N.

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201002741/fullpdf

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1. Transition Metal-Catalyzed Carbocyclizations in Organic Synthesis

2. Nickel-Catalyzed Cyclizations, Couplings, and Cycloadditions Involving Three Reactive Components

3. Nickel-katalysierte Kupplung von Carbonylverbindungen mit Alkinen oder 1,3-Dienen zu Allyl-, Homoallyl- und Bishomoallylalkoholen

4. Nickel-Catalyzed Coupling of Carbonyl Compounds and Alkynes or 1,3-Dienes: An Efficient Method for the Preparation of Allylic, Homoallylic, and Bishomoallylic Alcohols

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