A study of the Birch reduction of 4-methoxybenzoic acid

1968 ◽  
Author(s):  
William Court
Keyword(s):  
Birch Reduction ◽  
Methoxybenzoic Acid

Relations between Structure and Antituberculotic Activity of 4-Alkoxybenzoic Acids

1993 ◽  
Vol 58 (1) ◽  
pp. 191-196 ◽  
Author(s):  
Karel Waisser ◽  
Jiří Kuneš ◽  
Jiří Klimeš ◽  
Miroslav Polášek ◽  
Želmíra Odlerová
Keyword(s):  
Active Compound ◽  
Antimycobacterial Activity ◽  
Methoxybenzoic Acid

Antimycobacterial activity of a series of alkoxybenzoic acids including 4-methoxybenzoic acid (II), 4-ethoxybenzoic acid (III), 4-propoxybenzoic acid (IV), 4-butoxybenzoic acid (V), 4-pentoxybenzoic acid (VI), 4-allyloxybenzoic acid (IX), 4-isopropoxybenzoic acid (VII), 4-isobutoxybenzoic acid (VIII) and 4-benzyloxybenzoic acid (X) has been determined and found to increase with the lipophilicity of the compounds expressed by the corresponding HPLC capacity factors. Also determined were the pKa values of the compounds mentioned. The most active compound, 4-pentoxybenzoic acid (VI), is comparable with commercial antituberculotics when tested in vitro.

Silyl substituted furans in the stereoselective Birch reduction

2001 ◽  
Vol 42 (34) ◽  
pp. 5841-5844 ◽  
Author(s):  
Timothy J Donohoe ◽  
Jean-Baptiste Guillermin ◽  
Andrew A Calabrese ◽  
Daryl S Walter
Keyword(s):  
Birch Reduction ◽  
Substituted Furans

scholarly journals 2-Hydroxy-3-methoxybenzoic acid attenuates mast cell-mediated allergic reaction in mice via modulation of the FcεRI signaling pathway

2016 ◽  
Vol 38 (1) ◽  
pp. 90-99 ◽  
Author(s):  
Yeon-Yong Kim ◽  
In-Gyu Je ◽  
Min Jong Kim ◽  
Byeong-Cheol Kang ◽  
Young-Ae Choi ◽  
...  
Keyword(s):  
Mast Cell ◽  
Allergic Reaction ◽  
Signaling Pathway ◽  
Methoxybenzoic Acid

Asymmetric oxidations of enolates derived from Birch reduction of methyl 2-methoxybenzoate and (S)-2-methoxy-1-[[2'-(methoxymethyl)pyrrolidinyl]carbonyl]benzene

1992 ◽  
Vol 57 (10) ◽  
pp. 2973-2976 ◽  
Author(s):  
Arthur G. Schultz ◽  
Roger E. Harrington ◽  
Mark A. Holoboski
Keyword(s):  
Birch Reduction

Non-Mesogenic Behaviour of Para-n-Methoxybenzoic Acid: A Theoretical Study

1986 ◽  
Vol 55 (4) ◽  
pp. 1171-1176 ◽  
Author(s):  
Nitish K. Sanyal ◽  
Sugriva Nath Tiwari ◽  
Mihir Roychoudhury
Keyword(s):  
Theoretical Study ◽  
Methoxybenzoic Acid

scholarly journals Synthesis of ω-Hydroxy Ketones from ω-Benzyloxy Weinreb Amides by Using a Chemoselective Nucleophilic Addition/Birch Reduction Process.

ChemInform ◽  
2004 ◽  
Vol 35 (42) ◽  
Author(s):  
Catherine Taillier ◽  
Veronique Bellosta ◽  
Christophe Meyer ◽  
Janine Cossy
Keyword(s):  
Nucleophilic Addition ◽  
Reduction Process ◽  
Birch Reduction ◽  
Weinreb Amides ◽  
Hydroxy Ketones

The origin of the Birch reduction

1975 ◽  
Vol 52 (7) ◽  
pp. 458 ◽  
Author(s):  
A. J. Birch
Keyword(s):  
Birch Reduction
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