Artículos de revistas
Structure And Absolute Stereochemistry Of Pseudorepanduline. 13c-nmr Studies On Repanduline-type Alkaloids
Registro en:
Journal Of Natural Products. , v. 55, n. 4, p. 455 - 460, 1992.
1633864
2-s2.0-0026631375
Autor
Koike L.
Reis F.D.A.M.
Bick I.R.C.
Institución
Resumen
The 13C-nmr spectrum of repanduline was assigned from the known structure 2 by means of 13C-1H (HETCOR) 2D correlation experiments. Using data from repanduline in conjunction with 1H-1H (COSY) and HETCOR 2D studies on pseudorepanduline [1], the absolute stereochemistry of 1 has been determined. Some observations are made on the conformation of repanduline-type alkaloids and on their possible mode of biosynthesis. 55 4 455 460