Literature DB >> 30964216

Stereoselective Desymmetrization of gem-Diborylalkanes by "Trifluorination".

Nivesh Kumar1, Reddy Rajasekhar Reddy1, Ahmad Masarwa1.   

Abstract

An efficient and general method for the chemoselective synthesis of unsymmetrical gem-diborylalkanes is reported. This method is based on a late-stage desymmetrization through nucleophilic "trifluorination", providing chiral gem-diborylalkanes bearing a trifluoroborate group. The reaction offers a highly modular and diastereoselective approach towards the synthesis of gem-diborylcyclopropanes. The utility of the gem-diborylalkane building blocks was demonstrated by selective post-functionalization of the trifluoroborate group. These functionalizations include inter- and intra- Pd-catalyzed Suzuki-Miyaura coupling reactions.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Suzuki-Miyaura cross-coupling; cyclopropanes; desymmetrization; gem-diborylalkanes; organotrifluoroborate salts

Year:  2019        PMID: 30964216     DOI: 10.1002/chem.201901267

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


  2 in total

1.  α-Boryl Organometallic Reagents in Catalytic Asymmetric Synthesis.

Authors:  Chenlong Zhang; Weipeng Hu; James P Morken
Journal:  ACS Catal       Date:  2021-08-12       Impact factor: 13.700

2.  Stereoselective Cyclopropanation of 1,1-Diborylalkenes via Palladium-Catalyzed (Trimethylsilyl)diazomethane Insertion.

Authors:  Oriol Salvado; Paula Dominguez-Molano; Elena Fernández
Journal:  Org Lett       Date:  2022-07-07       Impact factor: 6.072

  2 in total

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