%0 Journal Article
%T An Efficient and Short Route for the Synthesis of Reverse Pyrrole Ribonucleosides
%A Pereira
%A Let¨ªcia O. R.
%A Cunha
%A Anna C.
%A Souza
%A Maria Cec¨ªlia B. V. de
%A Ferreira
%A Vitor F.
%J Journal of the Brazilian Chemical Society
%D 2002
%I Sociedade Brasileira de Qu¨ªmica, SBQ
%R 10.1590/S0103-50532002000300012
%X the synthesis of reverse pyrrole ribonucleosides methyl 5-c-(4-acetyl-5-methyl-pyrrol-1-yl)-2,3-o-isopropylidene-5-deoxy- b-d-ribofuranoside (10), methyl 5-c-(4-ethoxycarbonyl-5-methyl-pyrrol-1-yl)-2,3-o-isopropylidene-5-deoxy- b-d-ribofuranoside (11), methyl 5-c-(4-acetyl-5-methyl-pyrrol-1-yl)-5-deoxy-b-d-ribofuranoside (12), methyl 5-c-(4-ethoxycarbonyl-5-methyl-pyrrol-1-yl)-5-deoxy- b-d-ribofuranoside (13), methyl 5-deoxy-5-c-(3'-formyl-4'-hydroxypropyl-pyrrol-1'-yl)-2,3-o-isopropylidene- b-d-ribofuranoside (16) and methyl 5-deoxy-5-c-(3'-formyl-pyrrol-1'-yl)-2,3-o-isopropylidene- b-d-ribofuranoside (18) are described starting from readily available methyl 5-amino-5-deoxy-2,3-o-isopropylidene-b-d-ribofuranoside (9). the synthetic strategy for the construction of the heterocyclic ring was based on the nucleophilic attack of (9) to 4-acetyl-2-n-butoxy-5-methyl-4,5-dihydrofuran (4), 4-carbetoxy-2-n-butoxy-5-methyl-4,5-dihydrofuran (5), 4-formyl-2-n-butoxy-4,5-dihydrofuran (6) and 4-formyl-1-methyl dioxabyciclo[3.3.0]oct-3-en (8, in situ). the later compounds were obtained from reaction between 3-diazo-2,4-pentadione (1), ethyl 2-diazoacetoacetate (2) or diazomalonaldehyde (3) and enol ethers using dirhodium tetraacetate as a catalyst.
%K pyrrole nucleosides
%K reverse nucleosides
%K diazo
%K pyrrole.
%U http://www.scielo.br/scielo.php?script=sci_abstract&pid=S0103-50532002000300012&lng=en&nrm=iso&tlng=en