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1.	Foldesi, A, et al. (author) Selective cleavage of the O-6-diphenylcarbamoyl group from sugar-modified guanosines for incorporation into oligo-RNA 1999 In: TETRAHEDRON LETTERS. - : PERGAMON-ELSEVIER SCIENCE LTD. - 0040-4039. ; 40:40, s. 7283-7284 Journal article (other academic/artistic)abstract A facile conversion of 2',3',5'-O-tri-(Bz, Tol or Ac)-N-2-(Ac or iBu)-O-6-DPC-guanosine to N-2-(Ac or iBu)guanosine has been achieved in 89-98% yield by short treatment with 90% aqueous TFA for smooth cleavage of the DPC group followed by treatment with s
2.	Foldesi, A, et al. (author) Synthesis of partially-deuterated 2 '-deoxyribonucleoside blocks and their incorporation into an oligo-DNA for simplification of overcrowding and selective enhancement of resolution and sensitivity in the H-1-NMR spectra 1998 In: TETRAHEDRON. - : PERGAMON-ELSEVIER SCIENCE LTD. - 0040-4020. ; 54:48, s. 14487-14514 Journal article (other academic/artistic)abstract The chemical synthesis of appropriately protected partially-deuterated 2'((R) under bar/(S) under bar), 3',5'((R) under bar/(S) under bar)-H-2(3)-2'-deoxyribonucleoside blocks [similar to 43 atom % H-2 at C5'((R) under bar), similar to 57 atom % H-2 at C5
3.	Trifonova, A, et al. (author) Diastereospecific chemical synthesis of ribonucleosides-3 ',4 ',5 ',5 ''-d(4) 1999 In: TETRAHEDRON. - : PERGAMON-ELSEVIER SCIENCE LTD. - 0040-4020. ; 55:15, s. 4747-4762 Journal article (other academic/artistic)abstract The diastereospecific chemical syntheses of uridine-3',4',5',5"-d(4), cylidine-3',4',5',5''-d(4), adenosine-3',4',5',5"-d4 and guanosine-3',4',5',5"-d(4) (>97 atom % H-2 at C3', C4' and C5') have been achieved by condensation of appropriately protected ag

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Type of publication: journal article (3)

Type of content: other academic/artistic (3)Undo refine

Author/Editor: Chattopadhyaya, ... (3)Undo refine; Foldesi, A (3); Dinya, Z (3)Undo refine; Trifonova, A (2); Maltseva, TV (1)

University: Uppsala University (3)Undo refine

Language: English (3)

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