Literature DB >> 12916968

Enantioselective total synthesis of (+)-rogioloxepane A.

Michael T Crimmins1, Amy C DeBaillie.   

Abstract

[reactiojn: see text] The enantioselective synthesis of (+)-rogioloxepane A has been achieved in 21 steps from 1,5-hexadien-3-ol. The key steps in the synthesis are an asymmetric glycolate alkylation leading to the diene 2 and a subsequent ring-closing metathesis to construct the oxepene core.

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Year:  2003        PMID: 12916968     DOI: 10.1021/ol034923l

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


  3 in total

1.  Establishing the absolute configuration of the asbestinins: enantioselective total synthesis of 11-acetoxy-4-deoxyasbestinin D.

Authors:  Michael T Crimmins; J Michael Ellis
Journal:  J Am Chem Soc       Date:  2005-12-14       Impact factor: 15.419

2.  Total syntheses of (+)-vigulariol and (-)-sclerophytin A.

Authors:  Michael T Crimmins; Christina S Stauffer; Mark C Mans
Journal:  Org Lett       Date:  2011-08-19       Impact factor: 6.005

3.  Total synthesis of the proposed structure of briarellin J.

Authors:  Michael T Crimmins; Mark C Mans; Abimael D Rodríguez
Journal:  Org Lett       Date:  2010-11-05       Impact factor: 6.005

  3 in total

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