92118-50-8Relevant academic research and scientific papers
A TOTAL SYNTHESIS OF (+/-)-DIHYDROPALUSTRINE
Wasserman, Harry H.,Leadbetter, Michael R.,Kopka, Ihor E.
, p. 2391 - 2394 (1984)
Dihydropalustrine has been synthesized by a β-lactam-imino ether coupling route.A dehydro precursor previously considered to represent palustrine has now been shown to be nonidentical with the natural product.
A TOTAL SYNTHESIS OF (+/-)-ANHYDROCANNABISATIVINE.
Wassermann, Harry H.,Pearce, Bradley C.
, p. 2237 - 2240 (1985)
Racemic anhydrocannabisativine has been efficiently synthesized by employing a β-lactam-imino ether coupling reaction.The key to the formation of the tetrahydropyridine moiety of the natural alkaloid is a stereoselective intramolecular conjugate addition of a secondary amino group to a Z,E dienone.
A TOTAL SYNTHESIS OF (+/-)-ANHYDROCANNABISATIVINE.
Wasserman, Harry H.,Pearce, Bradley C.
, p. 3365 - 3372 (2007/10/02)
Racemic anhydrocannabisativine has been efficlently synthesized starting with a β-lactam-imino ether coupling reaction.A key step in the formation of the tetrahydopyridine moiety of anhydrocannabisativine is a stereoselective intramolecular conjugate addition of the N-11 amino group to a Z,E-dienone.
