Literature DB >> 23761321

A robust nickel catalyst for cyanomethylation of aldehydes: activation of acetonitrile under base-free conditions.

Sumit Chakraborty1, Yogi J Patel, Jeanette A Krause, Hairong Guan.   

Abstract

Nick of time: The nickel cyanomethyl complex 1 catalyzes the room temperature coupling of aldehydes with acetonitrile under base-free conditions. The catalytic system is long-lived and remarkably efficient with high turnover numbers (TONs) and turnover frequencies (TOFs) achieved. The mild reaction conditions allow a wide variety of aldehydes, including base-sensitive ones, to catalytically react with acetonitrile.
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  CH bond activation; aldol reaction; nickel; phosphane ligands; synthetic methods

Mesh:

Substances:

Year:  2013        PMID: 23761321     DOI: 10.1002/anie.201302613

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Palladium-catalyzed ligand-promoted site-selective cyanomethylation of unactivated C(sp3)-H bonds with acetonitrile.

Authors:  Yongbing Liu; Ke Yang; Haibo Ge
Journal:  Chem Sci       Date:  2016-01-06       Impact factor: 9.825

2.  Cu-catalyzed cyanomethylation of imines and α,β-alkenes with acetonitrile and its derivatives.

Authors:  Muhammad Siddique Ahmad; Atique Ahmad
Journal:  RSC Adv       Date:  2021-01-28       Impact factor: 3.361

  2 in total

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