SmI2-mediated reactions of diethyl iodomethylphosphonate with esters and lactones: a highly stereoselective synthesis of a precursor of the C-glycosyl analogue of thymidine 5′-(β-l-rhamnosyl)diphosphate-Reference-Cited by-同舟云学术

SmI2-mediated reactions of diethyl iodomethylphosphonate with esters and lactones: a highly stereoselective synthesis of a precursor of the C-glycosyl analogue of thymidine 5′-(β-l-rhamnosyl)diphosphate

Published:2002-09 Issue:40 Volume:43 Page:7259-7261
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Orsini Fulvia,Caselli Alessandro

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

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3. The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects

4. Total synthesis of gibberellic acid. A new and effective route to a key tricyclic intermediate

5. Asymmetric hydrogenation of β-ketophosphonates and β-ketothiophosphonates with chiral ru (II) catalysts

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