scholarly journals Unconjugated chiral azomethines; structure of N-isobutylidene derivatives of (S)-.ALPHA.-amino acid esters.

1978 ◽  
Vol 26 (2) ◽  
pp. 466-471 ◽  
Author(s):  
HIROSHI TAKAHASHI ◽  
HIROTAKA OTOMASU
Keyword(s):  
Amino Acid ◽  
Amino Acid Esters ◽  
Derivatives Of ◽  
Alpha Amino Acid ◽  
Acid Esters

Highly water-soluble derivatives of the anesthetic agent propofol: in vitro and in vivo evaluation of cyclic amino acid esters

2003 ◽  
Vol 20 (1) ◽  
pp. 17-26 ◽  
Author(s):  
Cosimo Altomare ◽  
Giuseppe Trapani ◽  
Andrea Latrofa ◽  
Mariangela Serra ◽  
Enrico Sanna ◽  
...  
Keyword(s):  
Amino Acid ◽  
Water Soluble ◽  
Anesthetic Agent ◽  
Amino Acid Esters ◽  
In Vivo Evaluation ◽  
Derivatives Of ◽  
Acid Esters

scholarly journals Aluminum-mediated one-pot conversion of .ALPHA.-amino acid esters to threo 2-amino alcohols with high diastereoselectivity.

1989 ◽  
Vol 37 (10) ◽  
pp. 2867-2869 ◽  
Author(s):  
Shinzo KANO ◽  
Yoko YUASA ◽  
Tsutomu YOKOMATSU ◽  
Shiroshi SHIBUYA
Keyword(s):  
Amino Acid ◽  
Amino Alcohols ◽  
Amino Acid Esters ◽  
One Pot ◽  
Alpha Amino Acid ◽  
Acid Esters

Synthesis of Amino Acid Esters: Derivatives of 1,2,3,4-Tetrahydroisoquinoline.

ChemInform ◽  
2005 ◽  
Vol 36 (23) ◽  
Author(s):  
N. N. Polygalova ◽  
A. G. Mikhailovskii
Keyword(s):  
Amino Acid ◽  
Amino Acid Esters ◽  
Derivatives Of ◽  
Acid Esters

Dimedone (5,5-Dimethylcyclohexane-1,3-dione) as a protecting agent for amino groups in peptide synthesis

1964 ◽  
Vol 17 (11) ◽  
pp. 1282 ◽  
Author(s):  
B Halpern ◽  
LB James
Keyword(s):  
Amino Acid ◽  
Peptide Synthesis ◽  
Amino Acid Esters ◽  
Protecting Group ◽  
Amino Groups ◽  
Active Esters ◽  
Optically Pure ◽  
Derivatives Of ◽  
Protected Peptides ◽  
Acid Esters

The reaction of dimedone (5,5-dimethylcyclohexane-1,3-dione) with amino-acid "active" esters leads to optically pure enamine derivatives. The dimedone derivatives of amino acid esters could also be converted by way of their hydrazides to the corresponding azides. The thiophenyl ester and azide derivatives have been used directly for peptide synthesis. The protecting group can easily be removed from the N-protected peptides by means of aqueous bromine, with the formation of 2,2-dibromodimedone and the hydrobromide of the corresponding peptide ester.

Derivatives of N-Carboxy-α-amino Acid Esters

1943 ◽  
Vol 65 (9) ◽  
pp. 1670-1674 ◽  
Author(s):  
Max Frankel ◽  
Ephraim Katchalski
Keyword(s):  
Amino Acid ◽  
Amino Acid Esters ◽  
Derivatives Of ◽  
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
Sign in / Sign up

Export Citation Format

Share Document