Lignans.19. Total synthesis of (−)-O-dimethylsugiresinol, involving asymmetric [4+2] heterocycloaddition of a styrene with a benzylidenepyruvic ester of an α-O-silyl derivative of (D)-erythronolactone-Reference-Cited by-同舟云学术

Lignans.19. Total synthesis of (−)-O-dimethylsugiresinol, involving asymmetric [4+2] heterocycloaddition of a styrene with a benzylidenepyruvic ester of an α-O-silyl derivative of (D)-erythronolactone

Published:1997-07 Issue:28 Volume:53 Page:9679-9694
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Brown Eric,Dujardin Gilles,Maudet Mickaël

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Lignans, neolignans, and related compounds

2. Enantioselective total synthesis of the di-O-methyl ethers of (–)-agatharesinol, (+)-hinokiresinol and (–)-sugiresinol, characteristic norlignans of Coniferae

3. First asymmetric synthesis of (−)-sugiresinol dimethyl ether

4. Synthesis of the (±)-dimethylethers of agatharesinol, sequirin-A, and hinokiresinol, related norlignans of coniferae.

5. Stereoselective total syntheses of the (±)-di-O-methyl ethers of agatharesinol, sesquirin-A, and hinokiresinol, and of (±)-tri-O-methylsequirin-E, characteristic norlignans of coniferae

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