Literature DB >> 23721303

An efficient protocol for the cross-metathesis of sterically demanding olefins.

Zhen J Wang1, W Roy Jackson, Andrea J Robinson.   

Abstract

Cross-metathesis of a wide range of previously unreactive, sterically demanding alkenes can be achieved in fair to excellent yield using a commercially available catalyst by a facile strategy involving reversal of steric preference.

Entities:  

Year:  2013        PMID： 23721303     DOI： 10.1021/ol401194h

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


  5 in total

1.  Rhodium-catalyzed endo-selective epoxide-opening cascades: formal synthesis of (-)-brevisin.

Authors:  Kurt W Armbrust; Matthew G Beaver; Timothy F Jamison
Journal:  J Am Chem Soc       Date:  2015-05-18       Impact factor: 15.419

2.  Synthesis of E- and Z-trisubstituted alkenes by catalytic cross-metathesis.

Authors:  Thach T Nguyen; Ming Joo Koh; Tyler J Mann; Richard R Schrock; Amir H Hoveyda
Journal:  Nature       Date:  2017-12-20       Impact factor: 49.962

3.  Bimolecular Cross-Metathesis of a Tetrasubstituted Alkene with Allylic Sulfones.

Authors:  Rishi R Sapkota; Jacqueline M Jarvis; Tanner M Schaub; Marat R Talipov; Jeffrey B Arterburn
Journal:  ChemistryOpen       Date:  2019-02-14       Impact factor: 2.911

4.  Synthesis of 2-aminosuberic acid derivatives as components of some histone deacetylase inhibiting cyclic tetrapeptides.

Authors:  Shital Kumar Chattopadhyay; Suman Sil; Jyoti Prasad Mukherjee
Journal:  Beilstein J Org Chem       Date:  2017-10-17       Impact factor: 2.883

5.  A Relay Strategy Actuates Pre-Existing Trisubstituted Olefins in Monoterpenoids for Cross-Metathesis with Trisubstituted Alkenes.

Authors:  Karim A Bahou; D Christopher Braddock; Adam G Meyer; G Paul Savage; Zhensheng Shi; Tianyou He
Journal:  J Org Chem       Date:  2020-03-19       Impact factor: 4.354
  5 in total

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