70963-39-2

Upstream product

• 67-56-1 methanol 
• 82038-34-4 (S)-2-((tert-butoxycarbonyl)(methyl)amino)-3-(4-hydroxyphenyl)propanoic acid 
• 112196-59-5 methyl N-(tert-butoxycarbonyl)-N-methyl-L-tyrosinate 
• 112196-57-3 methyl (S)-2-((tert-butoxycarbonyl)amino)-3-(4-((tert-butyldimethylsilyl)-oxy)phenyl)propanoate 
• 3417-91-2 L-tyrosine methyl ester HCl 
• 64263-81-6 N-(tert-butyloxycarbonyl)-N-methyl-O-(phenylmethyl)-L-tyrosine 
• 2130-96-3 O-benzyl-N-tert-butoxycarbonyl-L-tyrosine 
• 69955-04-0 methyl N-benzylidene-tyrosinate 
• 1080-06-4 L-Tyr-OMe 
• 866392-22-5 N-benzyl-N-methyl-L-tyrosine methyl ester 
• 111934-14-6 (S)-2-(2-Aza-bicyclo[2.2.1]hept-5-en-2-yl)-3-(4-hydroxy-phenyl)-propionic acid methyl ester 
• 537-49-5 N-methyl-L-tyrosine 
• 112196-58-4 (S)-methyl-2-((tert-butoxycarbonyl)(methyl)amino)-3-(4-((tert-butyldimethyl-silyl)oxy)phenyl)propanoate 
• 60-18-4 L-tyrosine 

Downstream Products

• 84254-47-7 methyl N-boc-N-methyl-L-tyr-N-methyl-L-tyrosinate 
• 113982-07-3 methyl 3-bromo-5-chloro-N-methyl-L-tyrosinate 
• 172036-67-8 methyl N-Boc-3-bromo-N-methyl-L-tyrosinate 
• 113982-06-2 methyl N-Boc-3-bromo-5-chloro-N-methyl-L-tyrosinate 
• 114014-11-8 methyl N-Cbz-3,5-dichloro-N-methyl-L-tyrosyl-3-bromo-5-chloro-N-methyl-L-tyrosinate 
• 112196-64-2 2-{[(S)-2-({(S)-2-[(S)-2-{[(S)-2-((R)-2-Amino-propionylamino)-propionyl]-methyl-amino}-3-(4-methoxy-phenyl)-propionylamino]-propionyl}-methyl-amino)-3-(4-hydroxy-phenyl)-propionyl]-methyl-amino}-3-(4-hydroxy-phenyl)-propionic acid; compound with trifluoro-acetic acid 
• 112196-65-3 C₅₁H₅₉F₅N₆O₁₂ 
• 112196-61-9 Boc-D-Ala-Ala-N-Me-Tyr(OMe)-Ala-N-Me-Tyr-N-Me-Tyr-OMe 
• 112196-62-0 Boc-D-Ala-Ala-N-Me-Tyr(OMe)-Ala-N-Me-Tyr-N-Me-Tyr-OH 
• 112196-60-8 H-N-Me-Tyr-N-Me-Tyr-OMe 
• 112196-67-5 C₄₆H₅₁F₅N₆O₁₀*C₂HF₃O₂ 
• 91475-02-4 methyl N-boc-N-methyl-L-tyr-N-methyl-L-tyr-D-ala-L-ala-O,N-dimethyl-L-tyr-L-alaninate 
• 91502-35-1 methyl N-methyl-L-tyr-N-methyl-L-tyr-D-ala-L-ala-O,N-dimethyl-L-tyr-L-alaninate 

Relevant academic research and scientific papers

Facile synthesis of highly functionalized N-methyl amino acid esters without side-chain protection

(Chemical Equation Presented) The facile, two-pot synthesis of N-methyl amino acid esters by way of reductive amination is presented. Side chain protection schemes are not required, the starting materials are all commercially available, and the synthetic

Immonium Ion Based Synthetic Methodology: A Novel Method for the N-Methylation of Dipeptides and Amino Acid Derivatives via Retro Aza Diels-Alder Reactions

A novel method for the N-methylation of amino acid derivatives and dipeptides is detailed that features facile room-temperature retro Diels-Alder reactions of N-substituted 2-azanorbornenes with trapping of the incipient immonium ion with triethylsilane/trifluoroacetic acid.

SYNTHESIS OF CYCLO-N-METHYL-L-TYR-N-METHYL-L-TYR-D-ALA-L-ALA-O,N-DIMETHYL-L-TYR-L-ALA, A CYCLIC HEXAPEPTIDE RELATED TO THE ANTITUMOR AGENT DEOXYBOUVARDIN

A synthesis of the title cyclic hexapeptide is described.Its lack of antitumor activity shows that the 14-membered ring of deoxybouvardin is needed for activity.Efforts to oxidatively its phenolic groups failed to give deoxybouvardin.

Tumor-resolving and histolytic medicaments and their use

Dehydrooligopeptides, some of which are known, demonstrate histolytic and tumor-resolving activity and may be used in medicaments causing the lysis of animal tissues and/or tumors in warm-blooded animals.