Samarium (II) Iodide-Mediated Intermolecular Coupling Reactions of N, N-Dibenzylenamides with Carbonyl Compounds and Transformation of the Product, N, N- …

Y AOYAGI, M MAEDA, A MORO, K KUBOTA…

Index: Aoyagi, Yutaka; Maeda, Mikiko; Moro, Akira; Kubota, Ken; Fujii, Yohko; Fukaya, Haruhiko; Ohta, Akihiro Chemical and Pharmaceutical Bulletin, 1996 , vol. 44, # 10 p. 1812 - 1818

Full Text: HTML

Citation Number: 5

Abstract

Samarium (II) iodide-mediated intermolecular coupling reactions of N, N-dibenzylenamides (1a-d) with carbonyl compounds (2a-i) produced the corresponding N, N-dibenzyl-γ- hydroxyamides (3a-i) in moderate to good yields. Attempts to remove the two benzyl groups of 3a using hydrogenolysis and Birch reduction were unsuccessful. On the other hand, the lithium aluminum hydride reduction of 3a produced 10 in 61% yield, and dedibenzylation ...

Related Articles:

A new synthesis of lactones from tertiary alkenylcarbinols by cobaltcatalyzed photocarbonylation under ambient conditions

[Chow, Yuan L.; Huang, Yu-Jin; Dragojlovic, Veljko Canadian Journal of Chemistry, 1995 , vol. 73, # 5 p. 740 - 742]

Metalated allylic ethers as homoenolate anion equivalents

[Evans,D.A. et al. Journal of the American Chemical Society, 1974 , vol. 96, # 17 p. 5560 - 5561]

Synthese de composes dihydro-2, 3 furanniques par hydroboration d'alcools β-acetyleniques

[Dana, Gilbert; Figadere, Bruno; Touboul, Estera Tetrahedron Letters, 1985 , vol. 26, # 46 p. 5683 - 5684]

More Articles...