ChemInform Abstract: INHIBITORS OF NEURONAL MONOAMINE UPTAKE. PART 2. SELECTIVE INHIBITION OF 5-HYDROXYTRYPTAMINE UPTAKE BY α-AMINO ACID ESTERS OF PHENETHYL ALCOHOLS

1978 ◽  
Vol 9 (46) ◽  
Author(s):  
U. H. LINDBERG ◽  
S. O. THORBERG ◽  
S. BENGTSSON ◽  
A. L. RENYI ◽  
S. B. ROSS ◽  
...  
Keyword(s):  
Amino Acid ◽  
Selective Inhibition ◽  
Amino Acid Esters ◽  
Monoamine Uptake ◽  
Acid Esters

Inhibitors of neuronal monoamine uptake. 2. Selective inhibition of 5-hydroxytryptamine uptake by .alpha.-amino acid esters of phenethyl alcohols

1978 ◽  
Vol 21 (5) ◽  
pp. 448-456 ◽  
Author(s):  
Ulf Henrik Lindberg ◽  
Seth Olof Thorberg ◽  
Stefan Bengtsson ◽  
Anna L. Renyi ◽  
Svante B. Ross ◽  
...  
Keyword(s):  
Amino Acid ◽  
Selective Inhibition ◽  
Amino Acid Esters ◽  
Monoamine Uptake ◽  
Alpha Amino Acid ◽  
Acid Esters

Asymmetric Preparation of anti-β-Hydroxyα-amino Acid Esters

Synfacts ◽  
2006 ◽  
Vol 2006 (12) ◽  
pp. 1253-1253
Author(s):  
Y. Hamada ◽  
K. Makino ◽  
M. Iwasaki
Keyword(s):  
Amino Acid ◽  
Amino Acid Esters ◽  
Acid Esters

Antiviral activity of glycyrrhizic acid conjugates with amino acid esters against Zika virus

2021 ◽  
Vol 294 ◽  
pp. 198290
Author(s):  
Lidia A. Baltina ◽  
Mann-Jen Hour ◽  
Ya-Chi Liu ◽  
Young-Sheng Chang ◽  
Su-Hua Huang ◽  
...  
Keyword(s):  
Amino Acid ◽  
Antiviral Activity ◽  
Zika Virus ◽  
Glycyrrhizic Acid ◽  
Amino Acid Esters ◽  
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.

ChemInform Abstract: CONVENIENT METHOD FOR THE PREPARATION OF N-CARBONYL-α-AMINO ACID ESTERS

1977 ◽  
Vol 8 (50) ◽  
pp. no-no
Author(s):  
YU. A. DAVIDOVICH ◽  
V. I. BUTAEVA ◽  
O. M. GALKIN ◽  
T. N. SENTSOVA ◽  
S. V. ROGOZHIN
Keyword(s):  
Amino Acid ◽  
Convenient Method ◽  
Amino Acid Esters ◽  
Acid Esters
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