Chemoselective reactions of vinylogous amides, and the synthesis of two peripentadenia alkaloids
JP Michael, AS Parsons
Index: Michael, Joseph P.; Parsons, Andrew S. Tetrahedron, 1996 , vol. 52, # 6 p. 2199 - 2216
Full Text: HTML
Citation Number: 17
Abstract
Some chemoselective transformations of the vinylogous amide (E)-2-benzoylmethylene-1-(2- cyano-ethyl) pyrrolidine (3a) and compounds derived from it have been investigated. Methodology developed during the course of these model studies has been applied to the synthesis of the alkaloids peripentadenme (1) and dinorperipentaclenine (2).
Related Articles:
The Fries Reaction of 2, 4-Dichloro-5-methylphenyl Acetate1
[Cremer,S.E.; Tarbell,D.S. Journal of Organic Chemistry, 1961 , vol. 26, p. 3653 - 3657]
Chromenones as potent bradykinin B1 antagonists
[Bryan, Marian C.; Biswas, Kaustav; Peterkin, Tanya A.N.; Rzasa, Robert M.; Arik, Leyla; Lehto, Sonya G.; Sun, Hong; Hsieh, Feng-Yin; Xu, Cen; Fremeau, Robert T.; Allen, Jennifer R. Bioorganic and Medicinal Chemistry Letters, 2012 , vol. 22, # 1 p. 619 - 622]