δ-Lactone formation from δ-hydroxy-trans-α,β-unsaturated carboxylic acids accompanied by trans–cis isomerization: synthesis of (−)-tetra-O-acetylosmundalin-Reference-Cited by-同舟云学术

δ-Lactone formation from δ-hydroxy-trans-α,β-unsaturated carboxylic acids accompanied by trans–cis isomerization: synthesis of (−)-tetra-O-acetylosmundalin

Published:2007-10 Issue:41 Volume:63 Page:10140-10148
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Ono Machiko,Zhao Xi Ying,Shida Yuki,Akita Hiroyuki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Chemoenzymatic syntheses of each stereoisomer of (4,5)-epoxy-(2E)-hexenoates

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3. The structure of U-13,933, a new antibiotic

4. New compounds from . X-ray crystal and molecular structures of anamarine

5. (+)-Osmundalactone, γ-lactones and spiromentins from the fungus Paxillus atrotomentosus

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