Younas Aouine, Hassane Faraj, Anouar Alami, Abdelilah El-Hallaoui, Abdelrhani Elachqar, Abdelali Kerbal
Index: Molecules 16 , 3380-3390, (2011)
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A simple synthetic approach to racemic N-tert-butyloxycarbonyl-2-methyl-3-(1H-1,2,4-triazol-1-yl)alanine (5) in four steps and 68% overall yield starting from oxazoline derivative 1 is reported. This synthesis involves the alkylation of 1H-1,2,4-triazole with an O-tosyloxazoline derivative, followed by an oxazoline ring-opening reaction and oxidation of the N-protected β‑aminoalcohol by potassium permanganate.
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
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1H-1,2,4-Triazole-5-propanoicacid, a-amino
CAS:10109-05-4 |
C5H8N4O2 |
|
Incorporation of amino acid analogs during the biosynthesis ...
1980-09-09 [Biochim. Biophys. Acta 615(1) , 59-69, (1980)] |
|
Synthesis of a novel histidine analogue and its efficient in...
2003-09-01 [Protein Eng. 16 , 699-706, (2003)] |
|
Classifying mutagens as to their specificity in causing the ...
1986-01-01 [Environ. Mutagen. 8 , 9, (1986)] |
|
Incorporation of an unnatural amino acid in the active site ...
1996-04-01 [Protein Eng. 9(4) , 345-52, (1996)] |
|
Incorporation of 1,2,4-triazole-3-alanine into a mutant of p...
1998-03-01 [Protein Eng. 11(3) , 213-7, (1998)] |
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