01272nas a2200229   4500008004100000022001400041245012800055210006900183260010600252300001400358490000700372520037200379653001400751653001700765653002300782653002500805653002300830100002100853700002100874700001900895856012800914       2012                        eng d  a0040-403900aStereospecific synthesis of C-arabinofuranosides and carba-disaccharide analogues of Motif C of cell wall AG complex of Mtb0 aStereospecific synthesis of Carabinofuranosides and carbadisacch  aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLANDbPERGAMON-ELSEVIER SCIENCE LTDcNOV  a6347-63500 v533 a<p>A simple strategy for the synthesis of alpha- and beta-C-arabinofuranosides featuring a furan ring transposition reaction has been developed. A novel double furan ring transposition reaction has proposed and executed for the synthesis of the carba-disaccharide analogue of Motif C of the cell wall AG complex of Mtb. (C) 2012 Elsevier Ltd. All rights reserved.</p>10aArabinose10aC-Glycosides10aCarba-disaccharide10aCell wall AG complex10aRing transposition1 aPatil, Rahul, S.1 aAhire, Ketan, M.1 aRamana, C., V.  uhttps://library.ncl.res.in/content/stereospecific-synthesis-c-arabinofuranosides-and-carba-disaccharide-analogues-motif-c-0