Enantio- and diastereocontrolled synthesis of (-)-19(S)-acetoxy-N1- acetyl-20-epitubifolidine

DOI: 10.1016/S0040-4039(98)00597-8

Source and publish data:

Tetrahedron Letters p. 3765 - 3768 (1998)

Update date:2022-08-03

Topics: Asymmetric synthesis Cyclization Retrosynthetic analysis Final steps Purification and Analysis Functional Group Transformations Protection and Deprotection Chiral Starting Materials Stereocontrolled Reactions Repetition and Optimization

Authors:

Shin, Kogyoku

Moriya, Minoru

Ogasawara, Kunio

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Article abstract of DOI:10.1016/S0040-4039(98)00597-8

An enantiocontrolled route to the 19-oxygenated pentacyclic Strychnos alkaloids has been demonstrated by the stereoselective synthesis of (-)- 19(S)-acetoxy-N₁-acetyl-20-epitubifolidine.

Full text of DOI:10.1016/S0040-4039(98)00597-8

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