Literature DB >> 15368920

A promising enantioselective Diels-Alder dienophile by computer-assisted rational design: 2,5-diphenyl-1-vinyl-borolane.

Silvina C Pellegrinet1, María A Silva, Jonathan M Goodman.   

Abstract

Several chiral vinylboranes have been theoretically evaluated as enantioselective Diels-Alder dienophiles. Theoretical results suggest that optically pure 2,5-diphenyl-1-vinyl-borolane should be the reagent of choice for performing such transformations efficiently.

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Year:  2004        PMID: 15368920     DOI: 10.1023/b:jcam.0000035200.30340.41

Source DB:  PubMed          Journal:  J Comput Aided Mol Des        ISSN: 0920-654X            Impact factor:   3.686


  1 in total

1.  Alkylhalovinylboranes: a new class of Diels-Alder dienophiles.

Authors:  Pablo L Pisano; Silvina C Pellegrinet
Journal:  RSC Adv       Date:  2018-10-02       Impact factor: 3.361

  1 in total

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