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

Tetrahedron Letters

Volumn 50, Issue 36, 2009, Pages 5088-5093

  Victoria Booth, K ^a   Jenkinson, Sarah F ^a   Best, Daniel ^a   Nieto, Fernando Fernández ^b   Estévez, Ramón J ^b   Wormald, Mark R ^c   Weymouth Wilson, Alexander C ^d   Fleet, George W J ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF SANTIAGO DE COMPOSTELA   (Spain)

^c UNIVERSITY OF OXFORD   (United Kingdom)

^d Dextra Laboratories Ltd   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

2 DEOXY 2,4 DI C METHYL ARABINOSE; 2,4 DI C METHYL ARABINOSE; 3 C METHYL ERYTHRONOLACTONE; ACETONE; ACETONIDE; ARABINOSE; CARBON; LACTONE DERIVATIVE; METHYL GROUP; PENTOSE; UNCLASSIFIED DRUG;

AQUEOUS SOLUTION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; ENANTIOMER; PROTON NUCLEAR MAGNETIC RESONANCE; QUANTUM YIELD; REACTION ANALYSIS; SYNTHESIS;

EID: 67650470447     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.06.098     Document Type: Article

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