Acta Cryst. (2004). E60, o1191-o1192  [ doi:10.1107/S1600536804013959 ]

A carbocyclic analogue of a protected -D-2-deoxyribosylamine

M. Ober, M. Marsch, K. Harms and T. Carell

Abstract: The title compound, tert-butyl N-[(1R,3S,4R)-3-hydroxy-4-(hydroxymethyl)cyclopentyl]carbamate, C₁₁H₂₁NO₄, is a very important intermediate for the enantioselective synthesis of carbocyclic analogues of 2'-deoxyribonucleotides. Its crystal structure proves that the relative substitution of the cyclopentane ring in this intermediate is the same as that in -2-deoxyribosylamine.

Online 19 June 2004

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