Literature DB >> 11856063

Efficient and convenient nonaqueous workup procedure for the preparation of arylboronic esters.

Ken-Tsung Wong1, Yuh-Yih Chien, Yuan-Li Liao, Chang-Chih Lin, Meng-Yen Chou, Man-kit Leung.   

Abstract

An efficient one-pot synthetic protocol for the synthesis of arylboronic esters has been established. The concentrated addition mixture of trimethylborate with aryl Grignard reagents was treated with low molecular weight diols (ethylene glycol, 1,3-propandiol) and toluene, the corresponding arylboronic esters were isolated in a convenient way with high yields. The diols not only serve as water replacement for the workup step, but also as well as the reagent for the preparation of arylboronic esters.

Entities:  

Year:  2002        PMID: 11856063     DOI: 10.1021/jo011073j

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


  3 in total

1.  Switching the selectivity of a polyglycerol dendrimer monomolecularly imprinted with D-(-)-fructose.

Authors:  Akihito Hashidzume; Steven C Zimmerman
Journal:  Tetrahedron Lett       Date:  2009-05-13       Impact factor: 2.415

2.  3-Cyanoallyl boronates are versatile building blocks in the synthesis of polysubstituted thiophenes.

Authors:  Wenjie Shao; Sherif J Kaldas; Andrei K Yudin
Journal:  Chem Sci       Date:  2017-04-18       Impact factor: 9.825

3.  Aminoboration: Addition of B-N σ Bonds across C-C π Bonds.

Authors:  Eugene Chong; Suzanne A Blum
Journal:  J Am Chem Soc       Date:  2015-08-10       Impact factor: 15.419

  3 in total

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