Literature DB >> 31799857

Coupling of Trifluoroacetaldehyde N-Triftosylhydrazone with Organoboronic Acids for the Synthesis of gem-Difluoroalkenes.

Yu Ma1,2, Bhoomireddy Rajendra Prasad Reddy1, Xihe Bi1,2.   

Abstract

The synthesis of alkyl gem-difluoroalkenes remains a difficult task in organic synthesis. Here, we report a general and efficient approach for tackling this problem by gem-difluoroolefination of trifluoroacetaldehyde N-triftosylhydrazone with organoboronic acids. This protocol is operationally simple, free of transition metals, and suitable for a broad range of organoboronic acids. Moreover, the utility of the products was demonstrated by further conversion of the gem-difluorovinyl group.

Entities:  

Year:  2019        PMID: 31799857     DOI: 10.1021/acs.orglett.9b03740

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Carbodefluorination of fluoroalkyl ketones via a carbene-initiated rearrangement strategy.

Authors:  Linxuan Li; Xinyu Zhang; Yongquan Ning; Xiaolong Zhang; Binbin Liu; Zhansong Zhang; Paramasivam Sivaguru; Giuseppe Zanoni; Shuang Li; Edward A Anderson; Xihe Bi
Journal:  Nat Commun       Date:  2022-07-25       Impact factor: 17.694

2.  Palladium-catalysed difluoroolefination of benzyl tosylates toward the synthesis of gem-difluoro-2-trifluromethyl styrene derivatives.

Authors:  Jie Xu; Jiangjun Liu; Gang Chen; Baojian Xiong; Xuemei Zhang; Zhong Lian
Journal:  RSC Adv       Date:  2022-04-28       Impact factor: 4.036

  2 in total

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