88815-92-3

Upstream product

• 88815-84-3 (S)-tert-Butyl 1-Oxo-3-phenyl-1-(pyrrolidin-1-yl)propan-2-ylcarbamate 

Downstream Products

• 118544-47-1 ((Z)-(S)-1-Benzyl-3-cyano-2-pyrrolidin-1-yl-allyl)-carbamic acid tert-butyl ester 
• 118544-40-4 ((Z)-(S)-1-Benzyl-4-oxo-2-pyrrolidin-1-yl-pent-2-enyl)-carbamic acid tert-butyl ester 
• 88815-84-3 (S)-tert-Butyl 1-Oxo-3-phenyl-1-(pyrrolidin-1-yl)propan-2-ylcarbamate 
• 125139-06-2 Ethyl (4S)-2-Cyano-4-(t-Boc-amino)-5-phenyl-3-(1-pyrrolidinyl)-2-pentenoate 
• 118544-42-6 ((Z)-(S)-1-Benzyl-4-naphthalen-2-yl-4-oxo-2-pyrrolidin-1-yl-but-2-enyl)-carbamic acid tert-butyl ester 
• 118579-66-1 ((Z)-(S)-3-Benzenesulfonyl-1-benzyl-2-pyrrolidin-1-yl-allyl)-carbamic acid tert-butyl ester 
• 118544-69-7 [(S)-1-((S)-1-Benzyl-3-cyano-2-oxo-propylcarbamoyl)-3-methyl-butyl]-carbamic acid tert-butyl ester 
• 118579-68-3 ((Z)-(S)-1-Benzyl-2-hydroxy-4-naphthalen-2-yl-4-oxo-but-2-enyl)-carbamic acid tert-butyl ester 
• 151214-76-5 [(Z)-(S)-1-Benzyl-2-hydroxy-3-(4-nitro-phenyl)-allyl]-carbamic acid tert-butyl ester 
• 118579-69-4 ((Z)-(S)-3-Benzenesulfonyl-1-benzyl-2-hydroxy-allyl)-carbamic acid tert-butyl ester 
• 118544-48-2 ((Z)-(S)-1-Benzyl-3-nitro-2-pyrrolidin-1-yl-allyl)-carbamic acid tert-butyl ester 
• 118544-44-8 ((Z)-(S)-1-Benzyl-4-oxo-2-pyrrolidin-1-yl-hexa-2,5-dienyl)-carbamic acid tert-butyl ester 
• 118544-60-8 (2E,4Z)-(S)-6-tert-Butoxycarbonylamino-5-hydroxy-7-phenyl-hepta-2,4-dienoic acid methyl ester 
• 118544-56-2 ((Z)-(S)-1-Benzyl-2-hydroxy-4-oxo-pent-2-enyl)-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

In Situ Reagent for Thionation of Amides, Peptides and Lactams

An in situ reagent 1A for thionation of amides, peptides and lactams is prepared from phosphorus decasulfide/sodium carbonate (1:1 ratio) in THF at 25 deg C.

FACILE REGIOSELECTIVE FORMATION OF THIOPEPTIDE LINKAGES FROM OLIGOPEPTIDES WITH NEW THIONATION REAGENTS

The thionation reagent 1 and the new more soluble and readily purified analogue 2 permit, in appropriate solvents, the low temperature backbone thionation of oligopeptides in a regioselective manner and in high yields.