Literature DB >> 20583043

Catalyst versus substrate induced selectivity: kinetic resolution by palladacycle catalyzed allylic imidate rearrangements.

René Peters1, Zhuo-qun Xin, Frank Maier.   

Abstract

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Year:  2010        PMID： 20583043     DOI： 10.1002/asia.201000386

Source DB:  PubMed          Journal:  Chem Asian J        ISSN： 1861-471X


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  4 in total

1.  Highly efficient gold(I)-catalyzed Overman rearrangement in water.

Authors:  Dong Xing; Dan Yang
Journal:  Beilstein J Org Chem       Date:  2011-06-08       Impact factor: 2.883

2.  Direct Enantioselective Addition of Alkynes to Imines by a Highly Efficient Palladacycle Catalyst.

Authors:  Camilla Pfeffer; Patrick Probst; Nick Wannenmacher; Wolfgang Frey; René Peters
Journal:  Angew Chem Int Ed Engl       Date:  2022-07-19       Impact factor: 16.823

3.  Enantioselective synthesis and application to the allylic imidate rearrangement of amine-coordinated palladacycle catalysts of cobalt sandwich complexes.

Authors:  Doyle J Cassar; Gennadiy Ilyashenko; Muhammad Ismail; James Woods; David L Hughes; Christopher J Richards
Journal:  Chemistry       Date:  2013-11-21       Impact factor: 5.236

4.  Stereospecific Asymmetric Synthesis of Tertiary Allylic Alcohol Derivatives by Catalytic [2,3]-Meisenheimer Rearrangements.

Authors:  Xin Yu; Nick Wannenmacher; René Peters
Journal:  Angew Chem Int Ed Engl       Date:  2020-04-30       Impact factor: 15.336
  4 in total

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