Archiv der Pharmazie

Hetero analogues of the antimicrobial alkaloids cleistopholine and sampangine

K Mink, F Bracher

Index: Bracher, Franz Archiv der Pharmazie (Weinheim, Germany), 1989 , vol. 322, p. 293 - 294

Full Text: HTML

Citation Number: 20

Abstract

Abstract Hetero analogues of the alkaloids cleistopholine and sampangine were prepared in order to investigate the significance of the (aza) quinoid partial structures for antimicrobial activity. Several analogues containing amino or sulfone groups showed high antimicrobial

Related Articles:

Regioselectivities in deprotonation of 2-(4-chloro-2-pyridyl) benzoic acid and corresponding ester and amide

[Rebstock, Anne-Sophie; Mongin, Florence; Trecourt, Francois; Queguiner, Guy Tetrahedron, 2004 , vol. 60, # 10 p. 2181 - 2186]

Using the Pummerer cyclization-deprotonation-cycloaddition cascade of imidosulfoxides for alkaloid synthesis

[Padwa, Albert; Heidelbaugh, Todd M.; Kuethe, Jeffrey T. Journal of Organic Chemistry, 2000 , vol. 65, # 8 p. 2368 - 2378]

Using the Pummerer cyclization-deprotonation-cycloaddition cascade of imidosulfoxides for alkaloid synthesis

[Padwa, Albert; Heidelbaugh, Todd M.; Kuethe, Jeffrey T. Journal of Organic Chemistry, 2000 , vol. 65, # 8 p. 2368 - 2378]

Using the Pummerer cyclization-deprotonation-cycloaddition cascade of imidosulfoxides for alkaloid synthesis

[Padwa, Albert; Heidelbaugh, Todd M.; Kuethe, Jeffrey T. Journal of Organic Chemistry, 2000 , vol. 65, # 8 p. 2368 - 2378]

Using the Pummerer cyclization-deprotonation-cycloaddition cascade of imidosulfoxides for alkaloid synthesis

[Padwa, Albert; Heidelbaugh, Todd M.; Kuethe, Jeffrey T. Journal of Organic Chemistry, 2000 , vol. 65, # 8 p. 2368 - 2378]

More Articles...