Literature DB >> 16758025

Control of ring size selectivity by substrate directable RCM.

Bernd Schmidt1, Stefan Nave.   

Abstract

Hydroxy groups may exert strong catalyst-directing effects in olefin metathesis reactions, which are exploited for a ring size-selective RCM reaction.

Year:  2006        PMID： 16758025     DOI： 10.1039/b604359c

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


  4 in total

1.  The catalytic performance of Ru-NHC alkylidene complexes: PCy₃versus pyridine as the dissociating ligand.

Authors:  Stefan Krehl; Diana Geißler; Sylvia Hauke; Oliver Kunz; Lucia Staude; Bernd Schmidt
Journal:  Beilstein J Org Chem       Date:  2010-12-15       Impact factor: 2.883

2.  Bidirectional cross metathesis and ring-closing metathesis/ring opening of a C 2-symmetric building block: a strategy for the synthesis of decanolide natural products.

Authors:  Bernd Schmidt; Oliver Kunz
Journal:  Beilstein J Org Chem       Date:  2013-11-18       Impact factor: 2.883

Review 3.  Sunscreen-Assisted Selective Photochemical Transformations.

Authors:  Or Eivgi; N Gabriel Lemcoff
Journal:  Molecules       Date:  2020-05-01       Impact factor: 4.411

4.  Light-Activated Olefin Metathesis: Catalyst Development, Synthesis, and Applications.

Authors:  Or Eivgi; Ravindra S Phatake; Noy B Nechmad; N Gabriel Lemcoff
Journal:  Acc Chem Res       Date:  2020-09-29       Impact factor: 22.384
  4 in total

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