01275nas a2200241   4500008004100000022001400041245008900055210006900144260007500213300001400288520041400302653001500716653002100731653001600752653001400768653001900782653002300801100001900824700002300843700002400866700002100890856012200911       2008                        eng d  a0039-788100aStereoselective synthesis of beta-C-Allyl- and beta-C-propargyl-D-arabinofuranosides0 aStereoselective synthesis of betaCAllyl and betaCpropargylDarabi  aRUDIGERSTR 14, D-70469 STUTTGART, GERMANYbGEORG THIEME VERLAG KGcJUN  a1783-17873 a<p>The stereoselective synthesis of beta-configured C-allyl- and C-propargyl-D-arabinofuranosides (4,7-anhydro-1,2,3-deoxy-D-gluco-oct-1-enitols and -oct-1-ynitols) was addressed by employing allylation/propargylation of a dialdofuranose under aqueous Barbier reaction conditions and acid-catalyzed furan ring transposition of 5-O-mesyl-manno-oct-7-eno- or 5-O-mesyl-manno-oct-7-ynofuranoside derivatives.</p>10aAllylation10aBarbier reaction10aC-glycoside10aD-mannose10apropargylation10aRing transposition1 aRamana, C., V.1 aNarute, Sachin, B.1 aGonnade, Rajesh, G.1 aPatil, Rahul, S.  uhttps://library.ncl.res.in/content/stereoselective-synthesis-beta-c-allyl-and-beta-c-propargyl-d-arabinofuranosides-0