Aza-nickelacycle key intermediate in nickel(0)-catalyzed transformation reactions-Reference-Cited by-同舟云学术

Aza-nickelacycle key intermediate in nickel(0)-catalyzed transformation reactions

Published:2015 Issue:27 Volume:44 Page:12060-12073
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Ohashi Masato¹²³⁴⁵,Hoshimoto Yoichi¹²³⁴⁵,Ogoshi Sensuke¹²³⁴⁵

Affiliation:

1. Department of Applied Chemistry

2. Faculty of Engineering

3. Osaka University

4. Suita

5. Japan

Abstract

Oxidative cyclization of alkynes and imines with nickel(0) is a key step in multicomponent coupling and cycloaddition reactions to give nitrogen-containing organic compounds.

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/DT/C5DT00640F

Reference92 articles.

1. Recent Advances in the Transition-Metal-Catalyzed Regioselective Approaches to Polysubstituted Benzene Derivatives

2. Construction of Pyridine Rings by Metal-Mediated [2 + 2 + 2] Cycloaddition

3. Transition Metal Catalyzed [2+2+2] Cycloaddition and Application in Organic Synthesis

4. [2+2+2] Cycloaddition Reactions Catalyzed by Transition Metal Complexes

5. Cationic Rhodium(I)/BINAP-Type Bisphosphine Complexes: Versatile New Catalysts for Highly Chemo-, Regio-, and Enantioselective [2+2+2] Cycloadditions

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