The first synthesis of (±)-cycloolivil: a highly stereoselective synthesis of 3-hydroxy-1-aryltetralin lignans based on the stereoselective hydroxylation of α,β-dibenzyl-γ-butyrolactones-Reference-Cited by-同舟云学术

The first synthesis of (±)-cycloolivil: a highly stereoselective synthesis of 3-hydroxy-1-aryltetralin lignans based on the stereoselective hydroxylation of α,β-dibenzyl-γ-butyrolactones

Published:1995 Issue:6 Volume: Page:671-672
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Moritani Yasunori,Ukita Tatsuzo,Ohmizu Hiroshi,Iwasaki Tameo

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1995/C3/C39950000671

Reference14 articles.

1. Lignans from bark of the Olea plants. I.

2. Isolation and Identification of (-)-Olivil and (+)-Cycloolivil fromStereospermum kunthianum

3. Introduction of an alcoholic hydroxyl group into 2,3-dibenzylbutyrolactone lignans with oxidizing agents and carbon-13 nuclear magnetic resonance spectra of the oxidation products.

4. Transformation of 2,3-dibenzylbutyrolactone lignans containing a secondary hydroxyl group to phenyltetralin lignans and their reduction products with lithium aluminum hydride.

5. A new two-step synthesis of 1-arylnaphthalene lignans from cyanohydrins

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