75548-48-0Relevant academic research and scientific papers
One-pot synthesis of aminoenone via direct reaction of the chloroalkyl enone with NaN3: Rapid access to polycyclic alkaloids
Zhao, Yu-Ming,Gu, Peiming,Tu, Yong-Qiang,Zhang, Hai-Jun,Zhang, Qing-Wei,Fan, Chun-An
supporting information; experimental part, p. 5289 - 5295 (2010/10/19)
(Figure presented) A new one-pot procedure for the preparation of aminoenone from chloroalkyl enone and sodium azide was demonstrated. The structure of the presumed triazoline intermediate in this process was confirmed by X-ray analysis for the first time. As the application of this methodology, the synthesis of polycyclic alkaloid hexahydroapoerysopine (1a) was achieved through an efficient synthetic route.
Six-membered-ring annulation via a conjugate addition/alkylation sequence using functionalized aryllithium reagents and vinyl sulfones
Ponton, John,Helquist, Paul,Conrad, Preston C.,Fuchs, Philip L.
, p. 118 - 122 (2007/10/02)
A new method, which is a one-flask procedure involving addition of substituted aryllithium reagents 6 to vinyl sulfones 8 and 9 followed by spontaneous intramolecular alkylation of the resulting α-lithio sulfones, has been developed for the annulation of tetrahydronaphtalene moieties onto preexisting carbon frameworks.The aryllithium reagents employed in this study are the previously investigated intermediates obtained by the chemoselective lithium-halogen exchange reactions of simple as well as oxygenated o-halo-β-phenethyl halides 5.The annulation products 11 and 12 may be subjected to various further transformations which should makethe overall sequences of considerable utility in the synthesis of steroids and other polycyclic systems.
