Literature DB >> 12613607

Enantioselective total synthesis of (-)-heliannuol A.

Hidetoshi Kishuku1, Mitsuru Shindo, Kozo Shishido.   

Abstract

An efficient and enantiocontrolled total synthesis of (-)-heliannuol A has been accomplished by employing ring closing metathesis and sequential diastereoselective epoxidation and regioselective reductive cleavage of the epoxide ring.

Entities:  

Year:  2003        PMID: 12613607     DOI: 10.1039/b211227b

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


  2 in total

1.  In Pursuit of an Ideal C-C Bond-Forming Reaction: Development and Applications of the Hydrovinylation of Olefins.

Authors:  T V Rajanbabu
Journal:  Synlett       Date:  2009       Impact factor: 2.454

2.  Biomimetic diversity-oriented synthesis of benzannulated medium rings via ring expansion.

Authors:  Renato A Bauer; Todd A Wenderski; Derek S Tan
Journal:  Nat Chem Biol       Date:  2012-11-18       Impact factor: 15.040

  2 in total

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