61177-53-5

Upstream product

• 32159-21-0 Cbz-L-pGlu-OH 
• 38596-35-9 dicyclohexylamine salt of N-benzyloxycarbonyl-(L)-pyroglutamic acid 
• 32159-21-0 1-benzyl hydrogen (S)-5-oxopyrrolidine-1,2-dicarboxylate 

Downstream Products

• 129416-04-2 (S)-2-{Allyl-[2-(tert-butyl-dimethyl-silanyloxy)-2-(3-methoxy-phenyl)-ethyl]-carbamoyl}-5-oxo-pyrrolidine-1-carboxylic acid benzyl ester 
• 176237-43-7 N-benzyloxycarbonyl-L-pyroglutamic acid isopropyl ester 
• 81910-23-8 (S)-N-Benzyloxycarbonyl-5-diazoacetylpyrrolidin-2-one 
• 65632-62-4 (3S)-hexahydro-1,3-pridazinedicarboxylic acid 1-(phenylmethyl) ester 
• 176237-44-8 isopropyl (S)-2-(benzyloxycarbonylamino)-5-hydroxypentanoate 
• 176237-45-9 isopropyl (S)-2-(benzyloxycarbonylamino)-5-(methanesulfonyloxy)pentanoate 
• 176237-47-1 isopropyl (S)-1-acetyl-2-benzyloxycarbonylhexahydropyridazine-3-carboxylate 
• 176237-46-0 isopropyl (S)-2-(2-acetyl-1-benzyloxycarbonylhydrazino)-5-(methanesulfonyloxy)pentanoate 
• 77400-63-6 (S)-2-[(Z)-1-((S)-2-Carbamoyl-pyrrolidine-1-carbonyl)-2-phenyl-vinylcarbamoyl]-5-oxo-pyrrolidine-1-carboxylic acid benzyl ester 
• 77400-61-4 2-((Z)-1-tert-Butoxycarbonyl-2-phenyl-vinylcarbamoyl)-5-oxo-pyrrolidine-1-carboxylic acid benzyl ester 
• 77400-59-0 C₁₉H₂₂N₄O₄ 
• 77400-62-5 2-((Z)-1-Carboxy-2-phenyl-vinylcarbamoyl)-5-oxo-pyrrolidine-1-carboxylic acid benzyl ester 
• 77400-60-3 (S)-2-((S)-1-tert-Butoxycarbonyl-2-phenyl-ethylcarbamoyl)-5-oxo-pyrrolidine-1-carboxylic acid benzyl ester 
• 319915-99-6 (S)-5-Acetoxyacetyl-N-benzoyloxycarbonylpyrrolidin-2-one 

Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS FOR USE IN THE TREATMENT OF CANCER

The application relates to heterocyclic amide derivatives and their use in the treatment and prophylaxis of cancer, and to compositions containing said derivatives and processes for their preparation. (Formula (I))

Synthesis of the necine base (-)-supinidine from (S)-glutamic acid

A report on the synthesis of the necine base (-)-supinidine from (S)-glutamic acid was presented. An approach using a Witting reaction to effect ring closure on to the carbonyl group of a succinimide derivative was reported. Melting points were obtained o

Adamantanamine derivatives, processes for their preparation and drugs in which they are present

The present invention relates to new adamantanamine derivatives. These derivatives correspond to the general formula I: STR1 in which: R represents hydrogen or a substituted or unsubstituted, linear or branched alkyl radical containing from 1 to 7 carbon

Synthesis of Dehydrothyroliberin, ΔZ-Phe2 -TRF

The first use of the N-chlorination-dehydrochlorination method in the synthesis of a dehydrodipeptide is reported in the preparation of the title compound.