Literature DB >> 19360169

Diastereoselective Ritter reactions of chiral secondary benzylic alcohols.

Philipp Rubenbauer1, Thorsten Bach.   

Abstract

An acid-catalysed Ritter reaction of chiral secondary benzylic alcohols enables diastereoselective access to chiral amides, which represent inter alia valuable intermediates for the synthesis of chiral 1,2-diamines and beta-amino acids.

Entities:  

Year:  2009        PMID： 19360169     DOI： 10.1039/b901937e

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


  4 in total

1.  Stereoinversion of tertiary alcohols to tertiary-alkyl isonitriles and amines.

Authors:  Sergey V Pronin; Christopher A Reiher; Ryan A Shenvi
Journal:  Nature       Date:  2013-09-12       Impact factor: 49.962

2.  A review of new developments in the Friedel-Crafts alkylation - From green chemistry to asymmetric catalysis.

Authors:  Magnus Rueping; Boris J Nachtsheim
Journal:  Beilstein J Org Chem       Date:  2010-01-20       Impact factor: 2.883

3.  Stereoretentive Copper (II) Catalyzed Ritter Reactions of Secondary Cycloalkanols.

Authors:  Mohammed H Al-Huniti; Salvatore D Lepore
Journal:  Adv Synth Catal       Date:  2013-10-11       Impact factor: 5.837

4.  A Direct and Stereoretentive Synthesis of Amides from Cyclic Alcohols.

Authors:  Deboprosad Mondal; Luca Bellucci; Salvatore D Lepore
Journal:  European J Org Chem       Date:  2011-12
  4 in total

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