Literature DB >> 27862463

Alkynylthioimidazolium Salts: Efficient Reagents for the Synthesis of Alkynyl Sulfides by Electrophilic Thioalkynylation.

Javier Peña1, Garazi Talavera1, Bernd Waldecker1, Manuel Alcarazo1.   

Abstract

The efficient synthesis of a series of alkynylthioimidazolium salts through reaction of organozinc compounds with dibromo(imidazolium)sulfuranes is reported. Addition of Grignard reagents to these new species provided a highly modular, clean, and scalable access to a broad variety of alkynyl sulfides in good-to-excellent yields. The utility of this protocol was showcased by the preparation of alkynyl sulfides, which are particularly difficult to obtain or simply unavailable through the existing methodologies. In addition, the synthetic method was extended to the preparation of alkynyl selenides.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  alkynylselenoethers; alkynylthioethers; alkynylthioimidazolium salts; electrophilic thioalkynylation; grignard reagents

Year:  2016        PMID: 27862463     DOI: 10.1002/chem.201604760

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  1 in total

1.  Donor Acceptor Complexes between the Chalcogen Fluorides SF2 , SeF2 , SeF4 and TeF4 and an N-Heterocyclic Carbene.

Authors:  Pascal Komorr; Marian Olaru; Emanuel Hupf; Stefan Mebs; Jens Beckmann
Journal:  Chemistry       Date:  2022-06-20       Impact factor: 5.020

  1 in total

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