Tetrahedron Letters p. 2217 - 2220 (1985)
Update date:2022-08-04
Topics:
Shibasaki, Masakatsu
Ishida, Yasuko
Okabe, Nobuko
A stereoselective synthesis of the known synthetic intermediate (13) for (-)-carpetimycin A (1) has been achieved starting from the monocyclic β-lactam (8b) by the novel use of the direct aldol condensation of 8b with acetone via the titanium enolate.
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Doi:10.1016/S0040-4020(01)96541-X
(1985)Doi:10.1016/j.tetlet.2004.08.035
(2004)Doi:10.1039/P19870000747
(1987)Doi:10.1021/jo00224a047
(1985)Doi:10.1021/jm00152a019
(1986)Doi:10.1016/S0040-4020(01)96551-2
(1985)
