Literature DB >> 23059706

Flow synthesis of arylboronic esters bearing electrophilic functional groups and space integration with Suzuki-Miyaura coupling without intentionally added base.

Aiichiro Nagaki1, Yuya Moriwaki, Jun-ichi Yoshida.   

Abstract

We found that an integrated flow microreactor system enables the preparation of boronic esters bearing electrophilic functional groups using organolithium chemistry and that it allows for their use in Suzuki-Miyaura cross-coupling without intentionally added base. Based on this method, cross-coupling of two aryl halides bearing electrophilic functional groups was accomplished to obtain the corresponding biaryl compounds in one flow.

Entities:  

Year:  2012        PMID: 23059706     DOI: 10.1039/c2cc36197c

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Alkoxyboration: ring-closing addition of B-O σ bonds across alkynes.

Authors:  Joshua J Hirner; Darius J Faizi; Suzanne A Blum
Journal:  J Am Chem Soc       Date:  2014-03-14       Impact factor: 15.419

2.  Catalyst-Free Synthesis of Borylated Lactones from Esters via Electrophilic Oxyboration.

Authors:  Darius J Faizi; Adena Issaian; Ashlee J Davis; Suzanne A Blum
Journal:  J Am Chem Soc       Date:  2016-02-16       Impact factor: 15.419

  2 in total

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