Synthesis of 4-substituted 1H-benzimidazole 2'-deoxyribonucleosides and utility of the 4-nitro compound as universal base

DOI: 10.1002/hlca.19960790216

Source and publish data:

Helvetica Chimica Acta p. 488 - 498 (1996)

Update date:2022-08-05

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Authors:

Seela Seela

Bourgeois

Rosemeyer

Wenzel Wenzel

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Article abstract of DOI:10.1002/hlca.19960790216

The stereoselective synthesis of 4-substituted 1H-benzimidazole 2'-deoxyribonucleosides is described. Regioisomeric (N¹ and N³) β-D-deoxyribonucleosides 2a-c and 3a-c were formed. ¹³C-NMR Chemical shifts of the 1H-benzimid

Full text of DOI:10.1002/hlca.19960790216

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