Resumen

MANCILLA PERCINO, Teresa  y  NIETO-ALVAREZ, David Aarón. Preparation and Characterization of Rosmarinecine Derivatives. J. Mex. Chem. Soc [online]. 2006, vol.50, n.4, pp.160-163. ISSN 1870-249X.

This work describes the synthesis of 8-tert-butyl-dimethylsilyloxy- (3), 2,8-bis(tert-butyldimethylsilyloxy)- (4) 2-mesyloxy-8-tert-butyldimethylsilyloxy- (5), and 2-tosyloxyros-marinecine (6) from selective protection of the different hydroxyl groups of rosmarinecine 2, which was obtained by hydrolysis of rosmarinine 1. The rosmarinine 1 naturally occuring was isolated in good yields (0.66%) from Senecio callosus. The chemoselectivity of the silylation of the hydroxyl groups at position C-2 and C-8 of 2 was controlled by the time of the reaction, which exhibited a higher reactivity for primary hydroxyl than secondary hydroxyl group, as well as the stereochemistry of the group at 1 position, which is trans and cis to the hydroxyl groups at 2 and 7 positions, respectively, where the steric efffect of hydroxyl group at 7 position is evidenced and possible effect of the solvent. The compounds were characterized by ¹H, ¹³C NMR, ¹H-¹H COSY, HETCOR spectra, infrared and mass spectrometry.

Palabras llave : Rosmarinecine derivatives; Hydroxypyrrolizidine; Pyrrolizidine; Alkaloids; Spectroscopy.

        · resumen en Español     · texto en Inglés     · Inglés ( pdf )