Literature DB >> 29469578

A Stereoselective Reductive Hosomi-Sakurai Reaction.

Adriano Bauer1, Nuno Maulide1.   

Abstract

A novel reductive variant of the classical Hosomi-Sakurai reaction is reported. This transformation hinges on a redox-neutral, stereoselective internal reduction event under mild conditions. This operationally simple reaction relies on readily available starting materials and leads to useful products in diastereoselectivities of up to 7:1. The versatility of this new method is demonstrated through the stereoselective one-step synthesis of an AChE inhibitor.

Entities:  

Year:  2018        PMID: 29469578     DOI: 10.1021/acs.orglett.8b00276

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


  2 in total

1.  Diastereo- and Enantioselective Access to Stereotriads through a Flexible Coupling of Substituted Aldehydes and Alkenes.

Authors:  Jing Li; Alexander Preinfalk; Nuno Maulide
Journal:  Angew Chem Int Ed Engl       Date:  2019-03-27       Impact factor: 15.336

2.  An α-Cyclopropanation of Carbonyl Derivatives by Oxidative Umpolung.

Authors:  Adriano Bauer; Giovanni Di Mauro; Jing Li; Nuno Maulide
Journal:  Angew Chem Int Ed Engl       Date:  2020-08-17       Impact factor: 16.823

  2 in total

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