143140-36-7

Upstream product

• 143140-35-6 (S)-N-(tert-butoxycarbonyl)-α-allyl-phenylalanine methyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 221617-21-6 (S)-α-allyl-phenylalanine methyl ester 
• 501380-80-9 (S)-N-allyloxycarbonyl-α-allyl-phenylalanine methyl ester 
• 100-39-0 benzyl bromide 
• 112741-50-1 (2S,3R)-tert-butyl 6-oxo-2,3-diphenylmorpholine-4-carboxylate 
• 143140-34-5 (S)-2-Benzyl-2-tert-butoxycarbonylamino-pent-4-enoic acid 
• 143140-30-1 (3R,5R,6S)-3-Benzyl-2-oxo-5,6-diphenyl-morpholine-4-carboxylic acid tert-butyl ester 
• 143140-31-2 (3S,5R,6S)-3-Allyl-3-benzyl-2-oxo-5,6-diphenyl-morpholine-4-carboxylic acid tert-butyl ester 

Downstream Products

• 1026522-06-4 2-benzyl-2-tert-butoxycarbonylamino-4-(methoxycarbonylmethyl-amino)-butyric acid methyl ester 
• 143140-38-9 ((3R,6R,7aS)-6-Benzyl-3-isobutylcarbamoyl-5-oxo-hexahydro-pyrrolo[2,1-b]thiazol-6-yl)-carbamic acid tert-butyl ester 
• 143140-37-8 (3R,6R,7aS)-6-Benzyl-6-tert-butoxycarbonylamino-5-oxo-hexahydro-pyrrolo[2,1-b]thiazole-3-carboxylic acid 

Relevant academic research and scientific papers

Synthesis and dopamine receptor modulating activity of 3-substituted γ-lactam peptidomimetics of L-prolyl-L-leucyl-glycinamide

γ-Lactam peptidomimetic 2 of Pro-Leu-Gly-NH2 (PLG) was substituted at the 3-position with isobutyl, butyl, and benzyl moieties to give the PLG peptidomimetics 3-5, respectively. These compounds were synthesized to test the hypothesis that attac

SYNTHESIS OF A BICYCLIC γ-LACTAM DIPEPTIDE ANALOGUE

The asymmetric synthesis of a bicyclic γ-lactam analogue of a dipeptide, in which the key step was the bis-alkylation of an optically active diphenyloxazinone chiral glycine anion equivalent is described.