Abstract

AbstractControl of the regioselective cyclisation of a stereodefined 5′‐C‐tosyloxy phosphorothioate dinucleotide unit to provide conformationally restricted dinucleotides of either thio‐dioxa‐ or oxo‐oxathiaphosphorinane types is described. NMR structural analysis of the newly synthesized building units showed the α and β torsional angles to be constrained to noncanonical values {gauche(+), trans} or {anticlinal(–), trans}.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)

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