Literature DB >> 12440925

Stereocartography: a computational mapping technique that can locate regions of maximum stereoinduction around chiral catalysts.

Kenny B Lipkowitz1, Cedric A D'Hue, Taka Sakamoto, Jonathan N Stack.   

Abstract

A hypothesis concerning asymmetric induction by chiral catalysts is posited, tested, and found to be valid. The hypothesis states that chiral catalysts that are efficient at inducing asymmetry will have their region of maximum stereoinduction spatially congruent with the site of chemistry but inefficient catalysts will not. A simple mapping strategy (stereocartography) is used to assess where the region of maximum stereoinduction is located around a given catalyst. The protocol compares interaction energies between mirror image probes at each point in space around the catalyst being considered. The probes are models of the actual transition states of the reaction being catalyzed by a particular catalyst. The hypothesis was tested on three Diels-Alder reactions. Seventeen of the eighteen catalysts conform to the hypothesis. The idea of using this as a catalyst design tool is presented.

Mesh:

Year:  2002        PMID: 12440925     DOI: 10.1021/ja0207192

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  5 in total

1.  Multidimensional steric parameters in the analysis of asymmetric catalytic reactions.

Authors:  Kaid C Harper; Elizabeth N Bess; Matthew S Sigman
Journal:  Nat Chem       Date:  2012-03-18       Impact factor: 24.427

2.  Predicting and optimizing asymmetric catalyst performance using the principles of experimental design and steric parameters.

Authors:  Kaid C Harper; Matthew S Sigman
Journal:  Proc Natl Acad Sci U S A       Date:  2011-01-24       Impact factor: 11.205

3.  A systematic investigation of quaternary ammonium ions as asymmetric phase-transfer catalysts. Synthesis of catalyst libraries and evaluation of catalyst activity.

Authors:  Scott E Denmark; Nathan D Gould; Larry M Wolf
Journal:  J Org Chem       Date:  2011-05-06       Impact factor: 4.354

Review 4.  Quantitative Structure-Selectivity Relationships in Enantioselective Catalysis: Past, Present, and Future.

Authors:  Andrew F Zahrt; Soumitra V Athavale; Scott E Denmark
Journal:  Chem Rev       Date:  2019-12-30       Impact factor: 60.622

5.  Computational design of high-performance ligand for enantioselective Markovnikov hydroboration of aliphatic terminal alkenes.

Authors:  Hiroaki Iwamoto; Tsuneo Imamoto; Hajime Ito
Journal:  Nat Commun       Date:  2018-06-12       Impact factor: 14.919

  5 in total

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