Nickel(0)-Catalyzed Formation of Oxaaluminacyclopentenes via an Oxanickelacyclopentene Key Intermediate: Me2AlOTf-Assisted Oxidative Cyclization of an Aldehyde and an Alkyne with Nickel(0)-Reference-Cited by-同舟云学术

Nickel(0)-Catalyzed Formation of Oxaaluminacyclopentenes via an Oxanickelacyclopentene Key Intermediate: Me2AlOTf-Assisted Oxidative Cyclization of an Aldehyde and an Alkyne with Nickel(0)

Published:2010-10-29 Issue:23 Volume:29 Page:6534-6540
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Ohashi Masato¹²,Saijo Hiroki¹,Arai Tomoya¹,Ogoshi Sensuke¹

Affiliation:

1. Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan

2. Center for Atomic and Molecular Technologies, Osaka University, Suita, Osaka 565-0871, Japan

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om100857a

Reference70 articles.

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

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

3. Nickel-Catalyzed Reductive Cyclizations and Couplings

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

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

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