708253-93-4

Upstream product

• 708253-99-0 [3-tert-butoxycarbonylamino-5-(tert-butyl-dimethyl-silanyloxy)-piperidin-1-yl]-acetic acid ethyl ester 
• 708253-91-2 tert-butyl N-[(3S,5R)-1-benzyl-5-[tert-butyl(dimethyl)silyl]oxy-3-piperidyl]carbamate 
• 708253-89-8 Methanesulfonic acid (3R,5R)-1-benzyl-5-(tert-butyl-dimethyl-silanyloxy)-piperidin-3-yl ester 
• 849161-65-5 tert-butyl N-[(3S,5R)-5-[tert-butyl(dimethyl)silyl]oxy-3-piperidyl]carbamate 
• 708253-90-1 [(3R,5S)-5-azido-1-benzyl-3-piperidyl]oxy-tert-butyl-dimethylsilane 
• 154429-40-0 (2S,4R)-1-benzyl-4-((tert-butyldimethylsilyl)oxy)pyrrolidine-2-carboxylic acid methyl ester 
• 154343-02-9 (2S,4R)-4-{[1-(tert-butyl)-1,1-dimethylsilyl]-oxy}-1-benzyl-2-hydroxy-methyl-pyrrolidin 
• 161564-09-6 (3R,5R)-1-benzyl-5-[(tert-butyldimethylsilyl)oxy]-piperidin-3-ol 
• 4330-20-5 N-3-benzoylthymine 
• 708253-92-3 ((3S,5R)-3-tert-Butoxycarbonylamino-5-hydroxy-piperidin-1-yl)-acetic acid ethyl ester 

Relevant academic research and scientific papers

Design and synthesis of conformationally frozen peptide nucleic acid backbone: Chiral piperidine PNA as a hexitol nucleic acid surrogate

The design and facile synthesis of novel chiral piperidine PNA from naturally occurring 4-hydroxy-L-proline is reported. The stereospecific ring-expansion reaction to get six-membered piperidine derivative from 5-membered pyrrolidine derivative is exploit

Piperidinyl peptide nucleic acids: Synthesis and DNA-complementation studies

Synthesis of a new six membered PNA analogue by introducing a methylene bridge between β carbon atom of ethylene diamine and β′ carbon atom of linker to nucleobase.