80514-79-0

Upstream product

• 1499-56-5 (R)-4-hydroxy-L-proline ethyl ester 
• 76-83-5 trityl chloride 
• 75-77-4 chloro-trimethyl-silane 
• 51-35-4 4-hydroxyproline 

Downstream Products

• 124456-35-5 5-triphenylmethyl-2-oxa-5-aza-bicyclo<2.2.1>heptan-3-one 
• 85918-11-2 N-Trt-Hyp 
• 85918-03-2 N-Trt-Hyp 
• 618-27-9 hydroxy L-proline 
• 129430-93-9 (2S,4S)-methyl 4-hydroxy-1-tritylpyrrolidine-2-carboxylate 
• 129431-00-1 cis-4-hydroxy-L-proline methyl ester 4-toluenesulfonate 
• 129431-02-3 cis-4-hydroxy-L-prolinamide 4-toluenesulfonate 
• 129518-77-0 3-oxo-2-oxa-5-azoniabicyclo<2.2.1>heptane 4-toluenesulfonate 
• 129430-95-1 cis-4-hydroxy-O-(4-tolylsulfonyl)-N-triphenylmethyl-L-proline methyl ester 
• 129430-96-2 cis-4-hydroxy-N-triphenylmethyl-L-proline amide 
• 129431-03-4 cis-4-hydroxy-N-triphenylmethyl-L-proline 

Relevant academic research and scientific papers

Synthesis and DNA-binding ability of C2R-fluoro substituted DC-81 and its dimers

C2R-Fluoro substituted DC-81 and its dimers have been synthesized that exhibit significant DNA-binding ability, particularly the five carbon alkane spacer compound (6c) showed the helix melting temperature (ΔTm) of 18.8 °C after incubation of 36 h at 37 °C.

Efficient "One-Pot" Synthesis of N-Trityl Amino Acids

A sequential procedure has been developed whereby neutral amino acids 1 were tritylated via their corresponding trimethylsilyl esters 2 to afford, after mild hydrolysis, N-trityl amino acids 3 in high yields and purity.Hydroxy amino acids 4 were preferent