73763-61-8

Upstream product

• 23234-86-8 N-(4-methoxybenzyloxycarbonyl)-L-phenylalanine 
• 3373-59-9 (2S,3S)-methyl 2-amino-3-hydroxybutanoate 
• 144664-88-0 (2S,3S)-2-((S)-2-Benzyloxycarbonylamino-3-phenyl-propionylamino)-3-hydroxy-butyric acid methyl ester 
• 73763-45-8 N-Boc-L-Phe-L-Thr-O-Me 
• 18942-49-9 Boc-D-Phe-OH 
• 3373-59-9 L-threonine methyl ester 
• 56936-27-7 Z(OMe)-Phe-Thr-OMe 

Downstream Products

• 144572-64-5 (2S,3S)-2-((S)-2-{(S)-2-[(S)-3-((2R,3R,4R,5R,6S)-3-Acetoxy-5-hydroxy-4-methoxy-6-methyl-tetrahydro-pyran-2-yloxy)-2-acetylamino-propionylamino]-3-hydroxy-propionylamino}-3-phenyl-propionylamino)-3-hydroxy-butyric acid methyl ester 
• 101854-20-0 Z(OMe)-Lys(Z)-Val-Pro-Ile-Phe-Thr-NHNH₂ 
• 101854-19-7 Z(OMe)-Lys(Z)-Val-Pro-Ile-Phe-Thr-OMe 
• 101854-11-9 Z(OMe)-Ser(Bzl)-Val-Pro-Ile-Phe-Thr-NHNH₂ 
• 101854-24-4 Z(OMe)-Ser(Bzl)-Val-Pro-Ile-Phe-Thr-OMe 
• 101854-29-9 Boc-Phe-Val-Pro-Ile-Phe-Thr-NHNH₂ 
• 101854-28-8 Boc-Phe-Val-Pro-Ile-Phe-Thr-OMe 
• 760132-68-1 Ile-Phe-Thr-OMe 

Relevant academic research and scientific papers

Total Synthesis of the Proposed Microcyclamides MZ602 and MZ568

The first convergent total synthesis for the proposed structures of microcyclamides MZ602 (1) and MZ568 (2) has been accomplished in 11 linear steps with 12.5 and 16.8% overall yield, respectively. Key features of the syntheses include a one-pot cascade r

Synthesis of a new serine containing glycotetrapeptide from Mycobacterium xenopi glycopeptidolipid : An unusual structural variant in mycobacterium genus

Synthesis of the unique glycotetrapeptide segment of Mycobacterium xenopi glycopeptidolipid is described.

Dehydrooligopeptides. IV. Synthesis of Various Types of Dehydrodi- and tripeptides by Fragment Condensation and Base-Catalyzed β-Elimination

The synthesis of dehydrotripeptides, composed of an α-amino acid and two α-dehydroamino acid (DHA) residues, by the direct coupling of N-protected δ1-dehydrotripeptide with DHA ester and by the β-elimination od δ1-dehydrodipeptide co