78700-18-2

Upstream product

• 60008-24-4 Boc-L-Ala-L-Hmb-OH 
• 78700-14-8 (S)-3-(4-Benzyloxy-phenyl)-2-[(S)-2-((S)-2-tert-butoxycarbonylamino-propionyloxy)-3-methyl-butyrylamino]-propionic acid 
• 65096-39-1 Boc-L-Ala-L-Hmb-ONSu 
• 4026-18-0 2-hydroxy-3-methylbutanoic acid 
• 66493-64-9 Boc-D-Dap(Z)-ONSu 
• 78700-16-0 (S)-2-[(S)-2-((S)-2-Amino-propionyloxy)-3-methyl-butyrylamino]-3-(4-benzyloxy-phenyl)-propionic acid; hydrochloride 

Downstream Products

• 78700-20-6 (S)-2-{(S)-2-[(S)-2-((R)-3-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-propionylamino)-propionyloxy]-3-methyl-butyrylamino}-3-(4-benzyloxy-phenyl)-propionic acid 2,5-dioxo-pyrrolidin-1-yl ester 
• 78700-23-9 (S)-2-{(S)-2-[(S)-2-((R)-2-Amino-3-benzyloxycarbonylamino-propionylamino)-propionyloxy]-3-methyl-butyrylamino}-3-(4-benzyloxy-phenyl)-propionic acid 2,5-dioxo-pyrrolidin-1-yl ester; compound with trifluoro-acetic acid 
• 78700-26-2 [9-(4-Benzyloxy-benzyl)-12-isopropyl-3-methyl-2,5,8,11-tetraoxo-1-oxa-4,7,10-triaza-cyclododec-6-ylmethyl]-carbamic acid benzyl ester 
• 78700-32-0 1>-AM-toxin 

Relevant academic research and scientific papers

SYNTHESES OF AM-TOXIN III AND ITS ANALOGS USING THE HOFMANN DEGRADATION

Syntheses of cyclotetradepsipeptides, AM-toxin III and two analogs, were achieved, in which the Hofmann degradation method was used in order to derive a dehydroalanine residue from a 2,3-diamiopropionic acid residue in cyclodepsipeptide presursors.