Reductive cleavage of aryl oxazolines to benzaldehydes and substituted toluenes

AI Meyers, RJ Himmelsbach…

Index: Meyers, A. I.; Himmelsbach, Richard J.; Reuman, Michael Journal of Organic Chemistry, 1983 , vol. 48, # 22 p. 4053 - 4058

Full Text: HTML

Citation Number: 40

Abstract

Aryl oxazolines as a vehicle for the elaboration of suitably functionalized aromatic rings has been demonstrated by this group and others during the past 12 years. l As a functional protecting group for carboxylic acids, the oxazoline plays an important role in carbon-carbon bond forming reactions. The oxazoline can serve in an electrophilic sense to activate the aromatic ring toward nucleophilic aromatic substitution or in a nucleophilic sense via ...

Related Articles:

Iridium??catalyzed direct dehydroxylation of alcohols

[Huang, Jian-Lin; Dai, Xi-Jie; Li, Chao-Jun European Journal of Organic Chemistry, 2013 , # 29 p. 6496 - 6500]

Nickel boride–mediated cleavage of 1, 3-dithiolanes: a convenient approach to reductive desulfurization

[Khurana, Jitender M.; Magoo, Devanshi Synthetic Communications, 2010 , vol. 40, # 19 p. 2908 - 2913]

Rhodium-Catalyzed Reductive Decyanation of Nitriles Using Hydrosilane as a Reducing Agent: Scope, Mechanism and Synthetic Application

[Tobisu, Mamoru; Nakamura, Ryo; Kita, Yusuke; Chatani, Naoto Bulletin of the Korean Chemical Society, 2010 , vol. 31, # 3 p. 582 - 587]

Reductive cleavage of aryl oxazolines to benzaldehydes and substituted toluenes

[Journal of Organic Chemistry, , vol. 48, # 22 p. 4053 - 4058]

The Huang-Minlon modification of Wolff-Kishner reduction in rapid and simple way using microwave technology

[Journal of the Indian Chemical Society, , vol. 79, # 11 p. 906 - 907]

More Articles...