A SYNTHESIS OF NATURALLY-OCCURRING ,2S,3R)-4-HYDROXYMETHYLCYCLOPENT-4-ENE-1,2,3-TRIOL UTILIZING THE CYCLIZATION OF A DIOXOLANYL RADICAL

Authors
ZIEGLER FE HARRAN PG
Citation
Fe. Ziegler et Pg. Harran, A SYNTHESIS OF NATURALLY-OCCURRING ,2S,3R)-4-HYDROXYMETHYLCYCLOPENT-4-ENE-1,2,3-TRIOL UTILIZING THE CYCLIZATION OF A DIOXOLANYL RADICAL, Synlett, (5), 1995, pp. 493-494
Citations number
23
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
5
Year of publication
1995
Pages
493 - 494
Database
ISI
SICI code
0936-5214(1995):5<493:ASON,>2.0.ZU;2-U
Abstract
A radical cyclization is employed in the synthesis of a biosynthetic p recursor of aristeromycin and neplanocin A. A derivative of L-tartaric acid is used as both the source of chirality and the carbon radical.