2791-03-9

Upstream product

• 50903-78-1 N^α-tert-butoxycarbonylseryltyrosine 
• 61039-38-1 serylmethionine methyl ester hydrochloride 
• 3262-72-4 (S)-N-(tert-butoxycarbonyl)serine 
• 3262-71-3 tert-butoxycarbonylserylmethionine methyl ester 
• 10285-64-0 N^α-tert-butoxycarbonylseryltyrosine methyl ester 
• 2491-18-1 (S)-methyl 2-amino-4-(methylthio)butanoate hydrochloride 
• 3417-91-2 L-tyrosine methyl ester HCl 
• 3850-40-6 N-Boc-DL-serine 
• 16118-36-8 methionine methyl ester hydrochloride 
• 3417-91-2 tyrosine methyl ester hydrochloride 
• 1172-65-2 2-(2-tert-Butoxycarbonylamino-3-hydroxy-propionylamino)-3-(4-hydroxy-phenyl)-propionic acid methyl ester 
• 3262-71-3 2-(2-tert-Butoxycarbonylamino-3-hydroxy-propionylamino)-4-methylsulfanyl-butyric acid methyl ester 
• 39747-65-4 2-tert-Butoxycarbonylamino-3-hydroxy-propionic acid 2,5-dioxo-pyrrolidin-1-yl ester 
• 556-02-5 ?Tyr 

Downstream Products

• 96627-23-5 N-(tert-butoxycarbonyl)-L-seryl-L-tyrosyl-L-seryl-L-methionine 
• 96627-24-6 N-<2-(methylsulfonyl)ethoxycarbonyl>-L-seryl-L-tyrosyl-L-seryl-l-methionine 
• 2791-02-8 Boc-Ser-Tyr-Ser-Met-N₂H₃ 
• 2791-02-8 {1-[1-[1-(1-Hydrazinocarbonyl-3-methylsulfanyl-propylcarbamoyl)-2-hydroxy-ethylcarbamoyl]-2-(4-hydroxy-phenyl)-ethylcarbamoyl]-2-hydroxy-ethyl}-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

USE OF THE SILYLATION REACTION IN SYNTHESIS OF FRAGMENT 1-4 OF THE ACTH SEQUENCE

A new effective method of synthesizing fragment 1-4 of the ACTH sequence ensuring a high overall yield of the desired product is proposed.This result is achieved thanks to the wide use of the silylation reaction in the synthesis, which has permitted a con

USE OF 2-ALKOXY-1-ALKOXYCARBONYL-1,2-DIHYDROQUINOLINES AS CONDENSING AGENTS IN THE SYNTHESIS OF INTERMEDIATE FRAGMENTS OF THE 1 - 4 SEQUENCE OF ACTH

The use of 2-alkoxy-1-alkoxycarbonyl-1,2-dihydroquinolines as a condensing agent in a number of stages in the synthesis of fragments of the 1 - 4 sequence of ACTH is considered.In a number of cases, these compounds have successfully replaced dicyclohexylc