Tetrahedron Letters p. 2741 - 2744 (1987)
Update date:2022-07-30
Topics:
Tadano, Kin-ichi
Hoshino, Masahide
Ogawa, Seiichiro
Suami, Tetsuo
The title compound, an enantiomerically pure carbocyclic portion of the antibiotic (-)-aristeromycin, has been synthesized from D-erythrose.The synthesis involves a transformation of the known carbocyclic analogue of β-L-arabinofuranose to the α-D-ribo fo
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Doi:10.1007/BF00758763
(1988)Doi:10.1016/S0040-4039(00)95739-3
(1987)Doi:10.1021/ja00194a027
(1989)Doi:10.1007/BF00956671
(1987)Doi:10.1021/jo00242a021
(1988)Doi:10.1016/j.bmc.2015.05.052
(2015)
