1571933-52-2

Upstream product

• 775-06-4 D/L-3-hydroxy-phenylalanine 
• 1571933-49-7 C₂₄H₄₁NO₅Si 
• 1571933-47-5 C₁₈H₂₇NO₅ 
• 174732-96-8 N^α-Boc-D,L-m-tyrosine 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 1571933-53-3 C₁₈H₂₆INO₅ 
• 1571933-55-5 C₂₇H₃₆INO₈S 
• 1571933-58-8 C₂₉H₄₀INO₉S 
• 1571933-60-2 C₂₀H₂₉ClINO₅ 
• 1571933-62-4 C₂₀H₂₉BrINO₅ 
• 1571933-71-5 C₂₄H₄₀INO₅Si 
• 1571933-73-7 C₂₄H₄₀INO₅Si 
• 1571933-82-8 C₂₄H₄₀BrNO₅Si 
• 1571933-84-0 C₁₈H₂₆BrNO₅ 
• 1571933-87-3 tert-butyl 2-(tert-butoxycarbonylamino)-3-(2-bromo-5-(2-(4-methylphenylsulfonyloxy)ethoxy)phenyl)propanoate 
• 1571933-89-5 C₂₇H₃₆BrNO₈S 
• 1571933-90-8 C₂₇H₃₆BrNO₈S 
• 1571933-94-2 C₁₈H₂₀INO₆S 
• 1571933-96-4 C₂₇H₄₉NO₅SiSn 

Relevant academic research and scientific papers

AROMATIC AMINO ACID DERIVATIVE AND POSITRON EMISSION TOPOGRAPHY (PET) PROBE UTILIZING SAME

A compound having a structure represented by the general formula (I): (wherein n is 0 or 1; R1 represents a hydrogen atom (only if n = 0), a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, an optionally substituted amino group, an o

TYROSINE DERIVATIVE AND METHOD FOR PRODUCING TYROSINE DERIVATIVE

The objective of the present invention is to provide a tyrosine derivative which is useful as a melatonin MT1 receptor antagonist, and a method for producing a specific tyrosine derivative with high yield by efficiently introducing an iodine atom at the para position of the phenolic hydroxy group in the benzene ring of tyrosine with good regioselectivity. The tyrosine derivative of the present invention is characterized in being represented by the following formula (I): wherein R1 is a protective group of the amino group and the like; R2 is a protective group of the carboxy group and the like; R3 is a hydrogen atom and the like; R4 is a halogen atom and the like; A is —(CH2)l—[Z(CH2)m]n—; X is a leaving group.