Literature DB >> 31187999

Diborative Reduction of Alkynes to 1,2-Diboryl-1,2-Dimetalloalkanes: Its Application for the Synthesis of Diverse 1,2-Bis(boronate)s.

Fumiya Takahashi1, Keisuke Nogi1, Takahiro Sasamori2, Hideki Yorimitsu1.   

Abstract

Reduction of alkynes with alkali metals in the presence of B2pin2 results in diboration of alkynes. Distinct from conventional dissolving metal hydrogenations, two carbon-boron bonds and also two carbon-alkali metal bonds can be constructed in one operation to form 1,2-diboryl-1,2-dimetalloalkanes. The 1,2-diboryl-1,2-dimetalloalkanes generated are readily convertible to a wide range of vicinal bis(boronate)s. In particular, oxidation of the 1,2-dianionic species provides ( E)-1,2-diborylalkenes, unique anti-selective diboration of alkynes being thus executed.

Entities:  

Year:  2019        PMID: 31187999     DOI: 10.1021/acs.orglett.9b01622

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


  1 in total

1.  Facile Multiple Alkylations of C60 Fullerene.

Authors:  Kazuhira Miwa; Shinobu Aoyagi; Takahiro Sasamori; Shogo Morisako; Hiroshi Ueno; Yutaka Matsuo; Hideki Yorimitsu
Journal:  Molecules       Date:  2022-01-10       Impact factor: 4.411

  1 in total

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