A convergent synthesis of the [4.4]-spiroacetal-γ-lactones cephalosporolides E and F-Reference-Cited by-同舟云学术

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A convergent synthesis of the [4.4]-spiroacetal-γ-lactones cephalosporolides E and F

Published:2011-02 Issue:5 Volume:67 Page:995-1001
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Brimble Margaret A.,Finch Orla C.,Heapy Amanda M.,Fraser John D.,Furkert Daniel P.,O’Connor Patrick D.

Funder

Maurice Wilkins Centre for Molecular Biodiscovery

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. Structures of the cephalosporolides B–F, a group of C10lactones from Cephalosporium aphidicola

2. Pd(II)-Mediated Alkynediol Spiroketalization: First Total Synthesis of (−)-Cephalosporolide E and (+)-Cephalosporolide F

3. Total Synthesis of (+)-Cephalosporolide E and (-)-Cephalosporolide F en route to Bassianolone

4. 10-Membered Macrolides from the Insect Pathogenic Fungus Cordyceps militaris BCC 2816

5. Bassianolone: an antimicrobial precursor of cephalosporolides E and F from the entomoparasitic fungus Beauveria bassiana

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