01176nas a2200241   4500008004100000022001400041245009500055210006900150260011100219300001200330490000600342520024800348653001600596653002100612653003500633653004400668653001900712100001400731700002100745700002800766700002300794856011700817       2010                        eng d  a1570-178600aSynthetic studies of superstolide A: a carbohydrate based synthesis of the C21-C26 segment0 aSynthetic studies of superstolide A a carbohydrate based synthes  aEXECUTIVE STE Y26, PO BOX 7917, SAIF ZONE, 1200 BR SHARJAH, U ARAB EMIRATESbBENTHAM SCIENCE PUBL LTDcDEC  a657-6600 v73 a<p>The synthesis of C21-C26 fragment of superstolide A, starting from D-glucose diacetonide, involving regioselective ring opening of epoxide by Grignard reagent and regioselective stereospecefic hydroboration oxidation has been described.</p>10aChiral pool10aPotent cytotoxic10aRegioselective epoxide opening10aStereoselective hydroboration-oxidation10aSuperstolide A1 aPal, Rita1 aRahaman, Hasibur1 aMohapatra, Debendra, K.1 aGurjar, Mukund, K.  uhttps://library.ncl.res.in/content/synthetic-studies-superstolide-carbohydrate-based-synthesis-c21-c26-segment-0