Literature DB >> 26816103

Palladium-Catalyzed Synthesis of α-Iminonitriles from Aryl Halides via Isocyanide Double Insertion Reaction.

Zhen-Bang Chen1, Ying Zhang1, Qing Yuan1, Fang-Ling Zhang1, Yong-Ming Zhu1, Jing-Kang Shen2.   

Abstract

An efficient one-pot synthesis of α-iminonitriles from readily available aryl halides via palladium-catalyzed double isocyanide insertion and elimination has been developed, without using various hypertoxic cyanides and excess oxidants. Furthermore, the utility of this reaction was demonstrated by the rapid total synthesis of quinoxaline and the reaction of functional groups exchanged with aryl halides.

Entities:  

Year:  2016        PMID: 26816103     DOI: 10.1021/acs.joc.5b02777

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  From Isocyanides to Iminonitriles via Silver-mediated Sequential Insertion of C(sp3)-H Bond.

Authors:  Huiwen Chi; Hao Li; Bingxin Liu; Rongxuan Ye; Haoyang Wang; Yin-Long Guo; Qitao Tan; Bin Xu
Journal:  iScience       Date:  2019-11-01

Review 2.  Recent Advances in Palladium-Catalyzed Isocyanide Insertions.

Authors:  Jurriën W Collet; Thomas R Roose; Bram Weijers; Bert U W Maes; Eelco Ruijter; Romano V A Orru
Journal:  Molecules       Date:  2020-10-23       Impact factor: 4.411

  2 in total

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