
Asian Journal of Chemistry p. 913 - 920 (2013)
Update date:2022-08-25
Topics:
Shankar
Mohan, H. Rama
Prasad, U. Viplava
Krishna, M. Hari
Rao, P. Mareswar
Lakshmikumar
Subbaraju, Gottumukkala V.
A general synthetic approach was developed for (±)-dinoprost (1), (±)-carboprost (2) and their analogs (3-5) through a key intermediate (6). Compound 6 can be converted into the target compounds in two or three steps. Diastereomeric separation was accomplished easily for obtaining (±) dinoprost. Separation of diastereomers was difficult for (±) carboprost and their analogs. Key intermediate 6 was obtained, in turn, from (±)-corey lactone.
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