An intramolecular azomethine ylide–alkene cycloaddition approach to pyrrolo[3,2-c]quinolines-synthesis of a C2-truncated martinelline model
摘要:
The hexahydropyrrolo[3,2-c]quinoline core found in the Martinella alkaloids was constructed through an intramolecular [3+2] azomethine ylide-alkene cycloaddition. Some chemical manipulations of the tricycle are reported. (C) 2001 Elsevier Science Ltd. AU rights reserved.
A Convenient Synthesis of ω-[(Arylphosphonomethyl)Amino] Alkylphosphonic and Carboxylic Acids via in Situ–Generated Arylideneaminoalkyl- Phosphonic or Carboxylic Acids
作者:Dariusz Cal
DOI:10.1080/10426500902994338
日期:2010.3.24
-[(Arylphosphonomethyl)amino]alkylphosphonic and carboxylic acids are prepared in an easy work-up procedure, by addition of diethyl phosphite to in situ-generated arylideneaminoalkylphosphonic or carboxylic acids followed by hydrolysis with hydrochloric acid.
Weygand,F. et al., Chemische Berichte, 1968, vol. 101, # 10, p. 3623 - 3641
作者:Weygand,F. et al.
DOI:——
日期:——
Singh, Netra Pal; Annand, Krishna Lal; Singh, Jagvir, Asian Journal of Chemistry, 2011, vol. 23, # 9, p. 4090 - 4092