Literature DB >> 28402116

Nickel-Catalyzed Direct Synthesis of Aryl Olefins from Ketones and Organoboron Reagents under Neutral Conditions.

Chuanhu Lei1, Yong Jie Yip1, Jianrong Steve Zhou1.   

Abstract

Nickel-catalyzed addition of arylboron reagents to ketones results in aryl olefins directly. The neutral condition allows acidic protons of alcohols, phenols, and malonates to be present, and fragile structures are also tolerated.

Entities:  

Year:  2017        PMID： 28402116     DOI： 10.1021/jacs.7b02742

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN： 0002-7863            Impact factor:   15.419


  2 in total

1.  Experimental and Computational Study of the ( Z)-Selective Formation of Trisubstituted Olefins and Benzo-Fused Oxacycles from the Ruthenium-Catalyzed Dehydrative C-H Coupling of Phenols with Ketones.

Authors:  Hanbin Lee; Manoj V Mane; Ho Ryu; Debashis Sahu; Mu-Hyun Baik; Chae S Yi
Journal:  J Am Chem Soc       Date:  2018-08-03       Impact factor: 15.419

2.  Nickel(0)-Catalyzed Decarbonylative Cross-Coupling of Aromatic Esters with Arylboronic Acids via Chelation Assistance.

Authors:  Zhenzhu Hu; Yuhang Wang; Peng Ma; Xiaqian Wu; Jianhui Wang
Journal:  ACS Omega       Date:  2022-06-13
  2 in total

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