172405-47-9

Upstream product

• 172405-46-8 methyl 2-(2-amino-6-chloro-9H-purin-9-yl)acetate 
• 14470-28-1 mono-4-methoxytrityl chloride 
• 10310-21-1 2-Amino-6-chloropurin 

Downstream Products

• 682752-95-0 {{2-[1-(4,4-Dimethyl-2,6-dioxo-cyclohexylidene)-ethylamino]-ethyl}-[2-(2-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-amino}-acetic acid 
• 864776-36-3 {{2-[1-(4,4-Dimethyl-2,6-dioxo-cyclohexylidene)-ethylamino]-ethyl}-[2-(2-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-amino}-acetic acid methyl ester 
• 176750-53-1 {[2-(9H-Fluoren-9-ylmethoxycarbonylamino)-ethyl]-[2-(2-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-amino}-acetic acid methyl ester 
• 172405-55-9 {[2-(9H-Fluoren-9-ylmethoxycarbonylamino)-ethyl]-[2-(2-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-amino}-acetic acid 
• 172405-48-0 [N²-(4-methoxytrityl)-guanin-9-yl]-acetic acid 

Relevant academic research and scientific papers

Dde-protected PNA monomers, orthogonal to Fmoc, for the synthesis of PNA-peptide conjugates

Peptide nucleic acids have become, arguably, one of the most interesting of DNA mimics. Herein the efficient solution phase synthesis of four novel 1-(4,4-dimethyl-2,6-dioxacyclohexylidene)ethyl/4-methoxytrityl (Dde/Mmt) protected PNA monomers is reported

Synthesis of polyamide nucleic acids (PNAs) using a novel Fmoc/Mmt protecting-group combination

The preparation of 9-Fluorenylmethoxycarbonyl(Fmoc) protected building blocks for the synthesis of polyamide nucleic acids (PNAs) is described. Use of 4-Methoxyphenyldiphenylmethyl (Mmt)-protecting groups for the exocyclic amino function of the nucleobase