139004-99-2

Upstream product

• 141774-61-0 piperidine-2-yl-methylcarbamic acid tert-butyl ester 
• 134807-28-6 2-[N-(tert-butoxycarbonyl)aminomethyl]pyridine 
• 141774-78-9 {(S)-5-tert-Butoxycarbonylamino-5-[((S)-1-tridecanoyl-piperidin-2-ylmethyl)-carbamoyl]-pentyl}-carbamic acid tert-butyl ester 
• 638-53-9 tridecanoic acid 
• 139004-97-0 {(S)-5-tert-Butoxycarbonylamino-5-[((S)-1-piperidin-2-ylmethyl)-carbamoyl]-pentyl}-carbamic acid tert-butyl ester 
• 3731-51-9 2-(Aminomethyl)pyridine 
• 135741-41-2 {(S)-5-Amino-1-[(1-tridecanoyl-piperidin-2-ylmethyl)-carbamoyl]-pentyl}-carbamic acid tert-butyl ester 
• 135741-41-2 {(R)-5-Amino-1-[(1-tridecanoyl-piperidin-2-ylmethyl)-carbamoyl]-pentyl}-carbamic acid tert-butyl ester 
• 141774-62-1 N-(tert-butoxycarbonyl)-N-([1-(1-oxotridecyl)-2-piperidinyl]methyl)amine 
• 141789-87-9 N([1-(1-oxotridecyl)-2-piperidinyl]methyl)amine 
• 106719-44-2 Boc-D-Lys-OH 
• 13734-28-6 Boc-Lys-OH 

Relevant academic research and scientific papers

Synthesis of (D)- And (L)-forms of differentially protected 2-piperidinemethanamine

(D)- and (L)-isomers of pipecolic acid were converted into (D)- and (L)-2-piperidinemethanamine using an efficient sequence. The amino groups were selectively protected for further functionalization.