Transformations of the 2,7-Seco aspidosperma alkaloid leuconolam, structure revision of epi-Leuconolam, and partial syntheses of leuconoxine and leuconodines A and F

Transformations of the 2,7-Seco aspidosperma alkaloid leuconolam, structure revision of epi-Leuconolam, and partial syntheses of leuconoxine and leuconodines A and F

Several transformations of the seco Aspidosperma alkaloid leuconolam were carried out. The based-induced reaction resulted in cyclization to yield two epimers, the major product corresponding to the optical antipode of a (+)-meloscine derivative. The structures and relative configuration of the pro...

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Bibliographic Details
Main Authors: Kam, T.S., Low, Y.Y., Hong, F.J., Lim, K.H., Thomas, N.F.
Format: Article
Published: American Chemical Society 2013
Subjects:
QD Chemistry
Online Access:http://eprints.um.edu.my/10379/
http://eprints.um.edu.my/10379/1/Transformations_of_the_2%2C7%2DSeco_Aspidosperma_Alkaloid_Leuconolam%2CStructure_Revision_of_epi%2DLeuconolam%2C_and_Partial_Syntheses_of_Leuconoxine_and_Leuconodines_A_and_F.pdf

Internet

http://eprints.um.edu.my/10379/
http://eprints.um.edu.my/10379/1/Transformations_of_the_2%2C7%2DSeco_Aspidosperma_Alkaloid_Leuconolam%2CStructure_Revision_of_epi%2DLeuconolam%2C_and_Partial_Syntheses_of_Leuconoxine_and_Leuconodines_A_and_F.pdf

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