Doubly carbon-branched pentoses: synthesis of both enantiomers of 2.4-di-C-methyl arabinose and 2-deoxy-2,4-di-C-methyl arabinose using only acetonide protection

An acetonide is the only protecting group used in the synthesis of both the enantiomers of 2,4-di-C-methyl arabinose and 2-deoxy-2,4-di-C-methyl arabinose via the enantiomeric 3-C-methyl-l-erythronolactone [from 2-C-methyl-d-ribono-lactone or d-ribose] and 3-C-methyl-d-erythronolactone [from d-tagat...

Täydet tiedot

Bibliografiset tiedot
Päätekijät: Booth, K, Jenkinson, S, Best, D, Fernandez Nieto, F, Estevez, R, Wormald, M, Weymouth-Wilson, A, Fleet, G
Aineistotyyppi: Journal article
Kieli:English
Julkaistu: 2009