Literature DB >> 11772092

Selective ring opening cross metathesis of cyclooctadiene and trisubstituted cycloolefins.

John P Morgan1, Christie Morrill, Robert H Grubbs.   

Abstract

[reaction: see text] The selective ring opening cross metathesis of 1,5-cyclooctadiene and trisubstituted cycloolefins with acroyl species is described. The ring-opened products contain electronically differentiated olefins suitable for additional metathesis reactions. Trisubstituted cycloolefins open regioselectively, placing the acroyl cap on the less-substituted terminus.

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Year:  2002        PMID: 11772092     DOI: 10.1021/ol016918s

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Rate enhanced olefin cross-metathesis reactions: the copper iodide effect.

Authors:  Karl Voigtritter; Subir Ghorai; Bruce H Lipshutz
Journal:  J Org Chem       Date:  2011-04-29       Impact factor: 4.354

2.  Metathesis Cascade Strategies (ROM-RCM-CM): A DOS approach to Skeletally Diverse Sultams.

Authors:  Kyu Ok Jeon; Dinesh Rayabarapu; Alan Rolfe; Kelly Volp; Iman Omar; Paul R Hanson
Journal:  Tetrahedron       Date:  2009-06-27       Impact factor: 2.457

  2 in total

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