Structure of Monocrotaline. VII. 1 Structure of Retronecine and Related Bases

R Adams, M Carmack, JE Mahan

Index: Adams et al. Journal of the American Chemical Society, 1942 , vol. 64, p. 2593

Full Text: HTML

Citation Number: 17

Abstract

The most objectionable feature to structure I for retronecine, as pointed out in a previous paper, lies in the results obtained upon esterification. One hydroxyl in retronecine esterifies very readily, more readily than would be anticipated from the usual secondary alcohol, and the other esterifies

Related Articles:

Organolanthanide-catalyzed hydroamination. A kinetic, mechanistic, and diastereoselectivity study of the cyclization of N-unprotected amino olefins

[Gagne, Michel R.; Stern, Charlotte L.; Marks, Tobin J. Journal of the American Chemical Society, 1992 , vol. 114, # 1 p. 275 - 294]

Hydroamination/cyclization of aminoalkenes using cationic zirconocene and titanocene catalysts

[Gribkov, Denis V.; Hultzsch, Kai C. Angewandte Chemie - International Edition, 2004 , vol. 43, # 41 p. 5542 - 5546]

Cyclization of aminyl radicals generated by anodic oxidation of lithium alkenylamides. Stereo-and regioselective synthesis of cis-l-alkyl-2, 5-disubstituted pyrrolidines

[Tokuda, Masao; Yamada, Yasufumi; Takagi, Toshiya; Suginome, Hiroshi; Furusaki, Akio Tetrahedron, 1987 , vol. 43, # 2 p. 281 - 296]

Rearrangement of α-Aminoketones during Clemmensen Reduction. V. Influence of Alkyl Substitution on the α-Carbon1, 2, 3

[Leonard; Barthel Journal of the American Chemical Society, 1950 , vol. 72, p. 3632,3635]

1, 7-Cyclobutanonorbornane system

[Lan, Alexander J. Y.; Quillen, Suzanne L.; Heuckeroth, Robert O.; Mariano, Patrick S. Journal of the American Chemical Society, 1984 , vol. 106, # 21 p. 6439 - 6440]

More Articles...