The Absence of Hydrogen Bonding in Two Benzoic Acid Esters as Indicated by their Infrared Transmission

1948 ◽  
Vol 70 (11) ◽  
pp. 3937-3937 ◽  
Author(s):  
Charles P. Adams ◽  
R. T. Lagemann
Keyword(s):  
Hydrogen Bonding ◽  
Benzoic Acid ◽  
Infrared Transmission ◽  
Acid Esters

Hydrogen bonding of benzoic acid esters to unesterified hydroxyl groups in nitrocellulose

1975 ◽  
Vol 19 (10) ◽  
pp. 2913-2915
Author(s):  
B. W. Brodman ◽  
M. P. Devine ◽  
M. T. Gurbarg
Keyword(s):  
Hydrogen Bonding ◽  
Benzoic Acid ◽  
Hydroxyl Groups ◽  
Acid Esters

Enantioselective Nucleophilic Aromatic Substitution Reaction of Azlactones to Synthesize Quaternary α-Amino Acid Derivatives

Synlett ◽  
2020 ◽  
Author(s):  
Xiaohua Liu ◽  
Yi Li ◽  
Hao Pan ◽  
Wang-Yuren Li ◽  
Xiaoming Feng
Keyword(s):  
Hydrogen Bonding ◽  
Charge Transfer ◽  
Amino Acid ◽  
Substitution Reaction ◽  
Nucleophilic Aromatic Substitution ◽  
Amino Acid Derivatives ◽  
Amino Acid Esters ◽  
Aromatic Substitution ◽  
Charge Transfer Interaction ◽  
Acid Esters

AbstractAn asymmetric organocatalytic nucleophilic aromatic substitution reaction of azlactones with electron-deficient aryls was established. A variety of α-aryl α-alkyl α-amino acid esters and peptides were obtained in decent yields and stereoselectivities. A new bifunctional catalytic mode involving charge-transfer interaction and hydrogen bonding is proposed to explain the enantioselectivity.

Reactivity of α-amino acids in the N-acylation with benzoic acid esters in aqueous dioxane

2010 ◽  
Vol 80 (5) ◽  
pp. 964-967 ◽  
Author(s):  
N. R. Ishkulova ◽  
L. E. Oparina ◽  
L. B. Kochetova ◽  
T. P. Kustova ◽  
N. V. Kalinina ◽  
...  
Keyword(s):  
Amino Acids ◽  
Benzoic Acid ◽  
Aqueous Dioxane ◽  
Acid Esters

Serinol-Based Benzoic Acid Esters as New Scaffolds for the Development of Adenovirus Infection Inhibitors: Design, Synthesis, and In Vitro Biological Evaluation

2020 ◽  
Author(s):  
Sarah Mazzotta ◽  
Judith Berastegui-Cabrera ◽  
Gabriele Carullo ◽  
Margarita Vega-Holm ◽  
Marta Carretero-Ledesma ◽  
...  
Keyword(s):  
Benzoic Acid ◽  
Biological Evaluation ◽  
Adenovirus Infection ◽  
Design Synthesis ◽  
Acid Esters

Photochemischer Abbau N-substituierter O-Alkylurethane / The Photolysis of N-Substituted O-Alkylurethanes

1973 ◽  
Vol 28 (5-6) ◽  
pp. 339-352 ◽  
Author(s):  
Hartmut Schultze
Keyword(s):  
Benzoic Acid ◽  
Alkyl Group ◽  
Aromatic Amines ◽  
Acid Ethyl Ester ◽  
Primary Amines ◽  
Carbamic Acid ◽  
Alkyl Esters ◽  
Primary Products ◽  
Acid Esters ◽  
Amino Benzoic Acid

The photolysis of N-aryl-carbamic acid alkyl esters in methanol was investigated. The primary products, amino-benzoic acid esters and aromatic amines, result from photo-Fries rearrangements and splitting processes.2,4,6-Trimethylphenyl-carbamic acid ethyl ester and N-alkyl-carbamic acid alkyl esters form photolysis products only through homolytic splitting reactions.The photooxidation of N-substituted urethanes has been investigated in tert.-butanol. The main products are primary amines and CO2.These initially formed compounds are then further oxidized. In the aliphatic substituted derivatives, oxidation of the N-alkyl group results followed homolytic bond splitting.

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