TY - JOUR
T1 - Synthesis of 3-deoxy-D-manno-octulosonic acid (KDO)
AU - Collins, Peter M.
AU - Overend, W. George
AU - Shing, Tony
PY - 1981
Y1 - 1981
N2 - 2,3:5,6-Di-O-isopropylidene-D-mannose has been converted by five sequential reactions (Wittig reaction, deacetonation, hydrogenation, lactonisation, and isopropylidenation) into 2,3-dideoxy-5,6:7,8-di-O-isopropylidene-D-octonolactone which in a Wasserman reaction gave an α-ketolactone from which KDO could readily be obtained by hydrolysis.
AB - 2,3:5,6-Di-O-isopropylidene-D-mannose has been converted by five sequential reactions (Wittig reaction, deacetonation, hydrogenation, lactonisation, and isopropylidenation) into 2,3-dideoxy-5,6:7,8-di-O-isopropylidene-D-octonolactone which in a Wasserman reaction gave an α-ketolactone from which KDO could readily be obtained by hydrolysis.
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U2 - 10.1039/C39810001139
DO - 10.1039/C39810001139
M3 - Article
AN - SCOPUS:37049098866
SN - 0022-4936
SP - 1139
EP - 1140
JO - Journal of the Chemical Society, Chemical Communications
JF - Journal of the Chemical Society, Chemical Communications
IS - 21
ER -