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...
Main Authors: | Booth, K, Jenkinson, S, Best, D, Fernandez Nieto, F, Estevez, R, Wormald, M, Weymouth-Wilson, A, Fleet, G |
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Format: | Journal article |
Sprog: | English |
Udgivet: |
2009
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Lignende værker
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2,4-di-C-methyl-alpha-L-arabinose monohydrate
af: Booth, K, et al.
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2-Deoxy-2,3-O-isopropylidene-2,4-di-C-methyl-β-l-arabinose
Udgivet: (2009-03-01) -
2-De-oxy-2,3-O-isopropyl-idene-2,4-di-C-methyl-β-l-arabinose.
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Udgivet: (2009) -
Anomeric stereospecific synthesis of 2 '-C-methyl beta-nucleosides; the Holy reaction of cyanamide with 2-C-methyl-D-arabinose
af: Jenkinson, S, et al.
Udgivet: (2007) -
Synthesis of C-glycosyl phosphonate derivatives of 4-amino-4-deoxy-α-ʟ-arabinose
af: Lukáš Kerner, et al.
Udgivet: (2020-01-01)