Literature DB >> 21699171

Total synthesis of isofregenedadiol.

Suresh E Kurhade1, Abbas I Sanchawala, Velayutham Ravikumar, Debnath Bhuniya, D Srinivasa Reddy.   

Abstract

The first total synthesis of isofregenedadiol, a bicyclic diterpene isolated from H. Viscosum, is reported starting from a D-(-)-pantolactone chiral pool. A one-pot quadruple reaction sequence comprising an enyne ring-closing metathesis/cross-metathesis/Diels-Alder/aromatization for the construction of a target skeleton is the highlight of the present synthesis.
© 2011 American Chemical Society

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Year:  2011        PMID: 21699171     DOI: 10.1021/ol201336x

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


  1 in total

Review 1.  Diversity-Oriented Approaches to Polycycles and Heterocycles via Enyne Metathesis and Diels-Alder Reaction as Key Steps.

Authors:  Sambasivarao Kotha; Arjun S Chavan; Deepti Goyal
Journal:  ACS Omega       Date:  2019-12-16
  1 in total

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