Syntheses via dihydro-1, 3-oxazines. VI. A carboxyl protecting group stable to the Grignard reagent. A new synthesis of carboxylic acids

AI Meyers, IR Politzer, BK Bandlish…

Index: Journal of the American Chemical Society, , vol. 91, p. 5886 - 5887

Full Text: HTML

Citation Number: 8

Abstract

... Journal of the American Chemical Society 9I:2I 1 ... Financial assistance from the Petroleum Research Fund, administered by the Ameri- can Chemical Society, Ciba Pharmaceutical Co., Hoff- man-LaRoche, and Warner-Lambert Research Institute is gratefully acknowledged. ...

Related Articles:

Oxidative Cleavage of Alkenes Using an In Situ Generated Iodonium Ion with Oxone as a Terminal Oxidant

[Thottumkara, Prem P.; Vinod, Thottumkara K. Organic Letters, 2010 , vol. 12, # 24 p. 5640 - 5643]

(2-Amino-phenyl)-amides of ω-substituted alkanoic acids as new histone deacetylase inhibitors

[Bioorganic and Medicinal Chemistry Letters, , vol. 14, # 1 p. 283 - 287]

Structurally simple trichostatin A-like straight chain hydroxamates as potent histone deacetylase inhibitors

[Journal of Medicinal Chemistry, , vol. 45, # 13 p. 2877 - 2885]

Liquid crystalline properties of cholesteryl. omega.-arylalkanoates

[Journal of Physical Chemistry, , vol. 88, # 11 p. 2387 - 2390]

(2-Amino-phenyl)-amides of ω-substituted alkanoic acids as new histone deacetylase inhibitors

[Bioorganic and Medicinal Chemistry Letters, , vol. 14, # 1 p. 283 - 287]

More Articles...