TY - JOUR
T1 - Synthetic studies of erythromycins. II. Enantiospecific synthesis of A C-10-C-13 segment of erythronolide a from D-ribose
AU - Kinoshita, Mitsuhiro
AU - Arai, Masayuki
AU - Tomooka, Katsuhiko
AU - Nakata, Masaya
N1 - Funding Information:
Acknowledgment: We are grateful to Prof. S. Umezawa, Institute of Bioorganic Chemistry, and Prof. H. Umezawa, Institute of Microbial Chemistry for their generous supports of our program. Financial support by the Ministry of Education, Science, and Culture (Grant-in-Aid for Special Research) is deeply acknowledged. We also are indebted to Mr. S. Nakada, Keio University for elemental analyses.
PY - 1986
Y1 - 1986
N2 - (3R,4R,5R)-5-0-Benzyl-2-iodo-3,4-0-isopropylidene-4-methyl-1-heptene-3,4,5-triol 3, a C-10-C-13 synthetic segment of erythronolide A (1) was enantiospecifically synthesized in sixteen steps and 8.3% overall yield from D-ribose.
AB - (3R,4R,5R)-5-0-Benzyl-2-iodo-3,4-0-isopropylidene-4-methyl-1-heptene-3,4,5-triol 3, a C-10-C-13 synthetic segment of erythronolide A (1) was enantiospecifically synthesized in sixteen steps and 8.3% overall yield from D-ribose.
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U2 - 10.1016/S0040-4039(00)84382-8
DO - 10.1016/S0040-4039(00)84382-8
M3 - Article
AN - SCOPUS:0022643036
SN - 0040-4039
VL - 27
SP - 1811
EP - 1814
JO - Tetrahedron Letters
JF - Tetrahedron Letters
IS - 16
ER -