185393-97-9

Upstream product

• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 

Downstream Products

• 185394-03-0 (S)-2-Dibenzylamino-N-{(S)-1-[2-(4-fluoro-3-nitro-phenyl)-ethylcarbamoyl]-2-phenyl-ethyl}-3-hydroxy-propionamide 
• 185394-02-9 (S)-2-Diallylamino-N-{(S)-1-[2-(4-fluoro-3-nitro-phenyl)-ethylcarbamoyl]-2-phenyl-ethyl}-3-hydroxy-propionamide 
• 185394-04-1 (4S,7S)-7-Benzyl-4-diallylamino-15-nitro-2-oxa-6,9-diaza-bicyclo[10.2.2]hexadeca-1⁽¹⁵⁾,12⁽¹⁶⁾,13-triene-5,8-dione 
• 185393-98-0 ((S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-{(S)-1-[2-(4-fluoro-3-nitro-phenyl)-ethylcarbamoyl]-2-phenyl-ethylcarbamoyl}-ethyl)-carbamic acid tert-butyl ester 
• 185393-99-1 ((S)-1-{(S)-1-[2-(4-Fluoro-3-nitro-phenyl)-ethylcarbamoyl]-2-phenyl-ethylcarbamoyl}-2-hydroxy-ethyl)-carbamic acid tert-butyl ester 
• 185394-01-8 (S)-2-Amino-N-{(S)-1-[2-(4-fluoro-3-nitro-phenyl)-ethylcarbamoyl]-2-phenyl-ethyl}-3-hydroxy-propionamide 

Relevant academic research and scientific papers

A convergent approach to cyclopeptide alkaloids: Total synthesis of sanjoinine G1

A general strategy for the synthesis of cyclopeptide alkaloids containing an endocyclic aryl-alkyl ether bond has been developed featuring a key intramolecular SNAr reaction. The importance of the N-terminal protective group in the realization

Ein neuer Ansatz zur Totalsynthese von Cyclopeptid-Alkaloiden

Keywords: Alkaloide; Atropisomerie; Cyclisierungen; Makrocyclen; Peptide