The Action of Alkaline Reagents upon Carbonyl Bridge Compounds. I

CFH Allen, JE Jones, JA VanAllan

Index: Allen; Jones; VanAllan Journal of the American Chemical Society, 1946 , vol. 68, p. 708

Full Text: HTML

Citation Number: 3

Abstract

Summary The sodium amalgam reduction of polyhydroxyand polymethoxyflavones leads to the same colored reduction products as the reduction of the corresponding flavanones. There is some evidence that some of the flavylium salt is formed in the former case, but this is not the predominant product.

Related Articles:

CuCl-mediated tandem CO insertion and annulation of 1, 4-dilithio-1, 3-dienes: formation of multiply substituted cyclopentadienones and/or their head-to-head dimers

[Luo, Qian; Wang, Chao; Zhang, Wen-Xiong; Xi, Zhenfeng Chemical Communications, 2008 , # 13 p. 1593 - 1595]

1, 1-cycloaddition of oxalyl dichloride with dialkenylmetal compounds: formation of cyclopentadienone derivatives by the reaction of 1, 4,-dilithio-1, 3-dienes or …

[Chen, Chao; Xi, Chanjuan; Jiang, Yanfeng; Hong, Xiaoyin Journal of the American Chemical Society, 2005 , vol. 127, # 22 p. 8024 - 8025]

Steric Effects and Spectra in the Tetracyclones

[Shapiro; Becker Journal of the American Chemical Society, 1953 , vol. 75, p. 4769,4771]

Steric Effects and Spectra in the Tetracyclones

[Shapiro; Becker Journal of the American Chemical Society, 1953 , vol. 75, p. 4769,4771]

Reactions of diphenylcyclopropenone and tetracyclones with potassium superoxide

[Neckers, Douglas C.; Hauck, Gerhard Journal of Organic Chemistry, 1983 , vol. 48, # 24 p. 4691 - 4695]

More Articles...