Literature DB >> 32903009

Enantioselective Syntheses of (Z)-6'-Boryl-anti-1,2-oxaborinan-3-enes via a Dienylboronate Protoboration and Asymmetric Allylation Reaction Sequence.

Jichao Chen1, Ming Chen1.   

Abstract

The enantioselective synthesis of 6'-boryl-anti-1,2-oxaborinan-3-enes is reported. A Cu-catalyzed highly stereoselective 1,4-protoboration of 1,1-bisboryl-1,3-butadiene is developed to generate (E)-α,δ-bisboryl-crotylboronate. The chiral phosphoric-acid-catalyzed asymmetric allylboration of aldehydes with the boron reagent produces 6'-boryl-anti-1,2-oxaborinan-3-enes with excellent Z-selectivities and enantioselectivities. The product contains a vinyl and alkyl boronate unit that can directly participate in a variety of subsequent transformations.

Entities:  

Year:  2020        PMID: 32903009     DOI: 10.1021/acs.orglett.0c02657

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


  1 in total

1.  Diastereo-, Enantio-, and anti-Selective Formation of Secondary Alcohol and Quaternary Carbon Stereocenters by Cu-Catalyzed Additions of B-Substituted Allyl Nucleophiles to Carbonyls.

Authors:  Emilie Wheatley; Joseph M Zanghi; Simon J Meek
Journal:  Org Lett       Date:  2020-11-18       Impact factor: 6.005

  1 in total

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