78700-27-3

Upstream product

• 4026-18-0 2-hydroxy-3-methylbutanoic acid 
• 60008-24-4 Boc-L-Ala-L-Hmb-OH 
• 78700-21-7 Boc-D-Dap(Z)-L-Ala-L-Hmb-L-Tyr(Me)-ONSu 
• 78700-19-3 Boc-D-Dap(Z)-L-Ala-L-Hmb-L-Tyr(Me)-OH 
• 78700-17-1 H-L-Ala-L-Hmb-L-Tyr(Me)-OH*HCl 
• 78700-15-9 (S)-2-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionyloxy)-3-methyl-butyrylamino]-3-(4-methoxy-phenyl)-propionic acid 
• 65096-39-1 Boc-L-Ala-L-Hmb-ONSu 
• 78700-25-1 (S)-2-{(S)-2-[(S)-2-((R)-2-Amino-3-benzyloxycarbonylamino-propionylamino)-propionyloxy]-3-methyl-butyrylamino}-3-(4-methoxy-phenyl)-propionic acid 2,5-dioxo-pyrrolidin-1-yl ester; compound with trifluoro-acetic acid 

Downstream Products

• 78700-29-5 cyclo (-D-Dap-L-Ala-L-Hmb-L-Tyr(Me)-)*HCl 
• 60008-08-4 1>-AM-toxin 
• 78700-31-9 [12-Isopropyl-9-(4-methoxy-benzyl)-3-methyl-2,5,8,11-tetraoxo-1-oxa-4,7,10-triaza-cyclododec-6-ylmethyl]-trimethyl-ammonium; iodide 

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.