934339-35-2Relevant articles and documents
Improvement of the synthesis of sugar phosphonates using microwave irradiations
Peyrottes, Suzanne,Gallier, Franck,Papillaud, Alain,Bejaud, Jerome,Perigaud, Christian
, p. 1513 - 1515 (2007)
Sugar and nucleoside phosphonates have been prepared using a microwave-assisted reaction. Results concerning optimization of the reaction for various substrates as well as comparison of thermal and microwave experimental conditions of the Michaelis-Arbuzov reaction is reported. Copyright Taylor & Francis Group, LLC.
Ex-chiral-pool synthesis of β-hydroxyphosphonate nucleoside analogues
Gallier, Franck,Peyrottes, Suzanne,Perigaud, Christian
, p. 925 - 933 (2008/02/13)
A new series of mononucleotide analogues bearing a nonhydrolysable P-C bond instead of the P-O phosphate linkage is presented. We intend to set up an approach that allows the synthesis of β-hydroxyphosphonate nucleoside analogues as a single diastereoisomer. In this respect, the key "sugar-phosphonate" intermediate was obtained through an Arbusov reaction from an iodosugar derivative in which the stereochemistry of the β-hydroxy group is determined by the choice of the starting material and remains in the resulting nucleotide analogues. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.