20890-93-1

Usage

InChI:InChI=1/C12H15NO6/c1-18-9-4-2-8(3-5-9)7-19-12(17)13-10(6-14)11(15)16/h2-5,10,14H,6-7H2,1H3,(H,13,17)(H,15,16)

Upstream product

• 56-45-1 L-serin 
• 59577-32-1 2-(4-methoxybenzyloxycarbonyloxyimino)-2-phenylacetonitrile 
• 18912-37-3 4-methoxybenzyl hydrazinecarboxylate 
• 31558-46-0 4-methoxybenzyl phenyl carbonate 
• 25474-85-5 4-methoxybenzyloxycarbonyl azide 
• 5680-80-8 methyl (2S)-2-amino-3-hydroxypropanoate hydrochloride 
• 20854-48-2 4-Methoxy-benzyloxycarbonylfluorid 

Downstream Products

• 4218-63-7 N-(4-Methoxybenzyloxycarbonyl)-O-benzyl-L-serine 
• 17896-38-7 N--O-<α,α,α-trifluor-1-benzyloxycarbonylamino-aethyl>-Ser-Phe 
• 17896-36-5 N--O-<α,α,α-trifluor-1-benzyloxycarbonylamino-aethyl>-Ser-Phe-methylester 
• 65003-69-2 [(S)-1-((S)-2-Benzyloxy-1-carbamoyl-ethylcarbamoyl)-ethyl]-carbamic acid 4-methoxy-benzyl ester 
• 67320-79-0 Z(OMe)-Ser(Bzl)-NH₂ 
• 83283-40-3 Z(OMe)-Ser-Tyr-NHNH₂ 
• 145458-74-8 Z(OMe)-Ser(Msib)-Ala-NH₂ 
• 145458-75-9 Z(OMe)-Ser(Mtb)-Ala-NH₂ 
• 173928-86-4 Z(OMe)-Ser-Arg(NO₂)-OBzl 
• 67321-04-4 N^α-p-Methoxybenzyloxycarbonyl-O-benzyl-L-serin 
• 83550-67-8 Z(OMe)-Ser-Ser-Glu(OBzl)-Ile-NHNH-Troc 
• 83550-66-7 Z(OMe)-Ser-Glu(OBzl)-Ile-NHNH-Troc 
• 83563-15-9 Z(OMe)-Ser-Asp(OBzl)-Ala-Ala-Val-NHNH-Troc 
• 145458-70-4 Z(OMe)-Ser(Msib)-OH 

Relevant academic research and scientific papers

Synthesis of oligopeptides as polynucleotide analogs

Several dipeptides which have a uracil moiety in their side chains were designed as nucleotide analogs. Oligopeptides obtained from the dipeptides as monomer units were water-soluble, but exhibited no hypochromic effect with poly A or poly dA.

A New Synthesis of O-Benzyl-L-serine

An efficient three-step procedure to prepare O-benzyl-L-serine from serine in 85percent overall yield using the 4-methoxybenzyloxycarbonyl group for N-protection.