Literature DB >> 29192787

Highly Diastereoselective Cationic Cyclization Reactions Convert a Common Monocyclic Enone to Bicyclic Precursors for the Synthesis of Retigeranic Acids A and B.

Simon Breitler1, Yixin Han1, E J Corey1.   

Abstract

A novel method is demonstrated for the diastereoselective conversion of a monocyclic enone to a pair of bicyclic intermediates which enable the stereocontrolled enantioselective syntheses of retigeranic acids A and B.

Entities:  

Year:  2017        PMID： 29192787     DOI： 10.1021/acs.orglett.7b03412

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


  1 in total

1.  Domino ring-opening-ring-closing enyne metathesis vs enyne metathesis of norbornene derivatives with alkynyl side chains. Construction of condensed polycarbocycles.

Authors:  Ritabrata Datta; Subrata Ghosh
Journal:  Beilstein J Org Chem       Date:  2018-10-25       Impact factor: 2.883
  1 in total

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