Literature DB >> 17520110

Enantioselectivity in the boron aldol reactions of methyl ketones.

Jonathan M Goodman1, Robert S Paton.   

Abstract

DFT computed transition states quantitatively explain the surprising stereochemical outcome of unsubstituted enolborinates in diastereoselective and enantioselective boron aldol reactions.

Entities:  

Year:  2007        PMID： 17520110     DOI： 10.1039/b704786j

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


  2 in total

1.  (Diisopinocampheyl)borane-mediated reductive aldol reactions of acrylate esters: enantioselective synthesis of anti-aldols.

Authors:  Christophe Allais; Philippe Nuhant; William R Roush
Journal:  Org Lett       Date:  2013-07-25       Impact factor: 6.005

2.  Wittig Rearrangements of Boron-Based Oxazolidinone Enolates.

Authors:  Zirong Zhang; David B Collum
Journal:  J Org Chem       Date:  2019-08-15       Impact factor: 4.354
  2 in total

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