Transformations of lignans. Part 10: Acid-catalysed rearrangements of arboreol and wodeshiol and conversion of gmelanone oxime into a dihydropyranone derivative-Reference-Cited by-同舟云学术

Transformations of lignans. Part 10: Acid-catalysed rearrangements of arboreol and wodeshiol and conversion of gmelanone oxime into a dihydropyranone derivative

Published:2005-09 Issue:37 Volume:61 Page:8956-8961
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Venkateswarlu Revuru,Kamakshi Chakicherla,Subhash Pithani V.,Moinuddin Syed G.A.,Gowri Mangala P.,Ward Robert S.,Pelter Andrew,Hursthouse Michael B.,Coles Simon J.,Light Mark E.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference12 articles.

1. Acid catalysed rearrangements of arboreol: A biomimetic synthesis of gmelanone

2. Reaction of gmelinol with triethylsilane and BF3-etherate - rearrangement of the 2.6-diaryl-3,7-dioxabicyclo[3.3.0]octane skeleton

3. Oxidative transformations of lignans - reactions of dihydrocubebin and a derivative with DDQ

4. Rearrangements of 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans reactions of paulownin and wodeshiol with triethylsilane and BF3-etherate

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