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An easy access to a 3,6-branched mannopentaoside bearing one terminal [1-13C]-labeled D-mannopyranose residue
Authors:P. I. Abronina  L. V. Backinowsky  A. A. Grachev  S. L. Sedinkin  N. N. Malysheva
Affiliation:(1) N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation
Abstract:Methyl 2,4-di-O-benzoyl-α-D-mannopyranoside was used as a key intermediate in the synthesis of 3,6-branched mannopentaoside bearing one terminal D-[1-13C]mannopyranose residue, viz., methyl 6-O-[3,6-di-O-(α-D-mannopyranosyl)-α-D-mannopyranosyl)-3-O-{α -D-[1-13C]mannopyranosyl}-α-D-mannopyranoside. Dedicated to Academician N. K. Kochetkov on the occasion of his 90th birthday. __________ Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 1250–1255, May, 2005.
Keywords:methyl 2,4-di-O-benzoyl-α  -  font-variant:small-caps"  >D-mannopyranoside  3,6-branched mannooligosaccharides     font-variant:small-caps"  >D-[1-13C]mannopyranose  [1-13C]-labeled mannopentaoside  selective glycosylation  selective deacylation
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