405506-75-4

Upstream product

• 405506-67-4 (2S,3S,6R)-6-allyl-3-benzyloxy-2-(tert-butyldiphenylsilyloxymethyl)-1-tosylpiperidine 
• 405506-65-2 (2S,3S,6R)-3-benzyloxy-2-(tert-butyldiphenylsilyloxymethyl)-6-ethoxy-1-tosylpiperidine 
• 405506-69-6 (2S,3S,6R)-[5-benzyloxy-6-(tert-butyldiphenylsilyloxymethyl)-1-tosylpiperidin-2-yl]acetaldehyde 
• 405506-73-2 (4R)-4-(8-bromooctyl)-2,2-dimethyl-[1,3]dioxolane 
• 405506-71-0 (2R)-10-bromodecane-1,2-diol 
• 258531-66-7 (2S,3S,6R)-2-(tert-Butyldiphenylsilyloxymethyl)-6-ethoxy-1-tosylpiperidin-3-ol 
• 124388-97-2 9-bromononanal 
• 62871-09-4 10-bromodec-1-ene 
• 100-39-0 benzyl bromide 
• 3937-56-2 1,9-Nonanediol 
• 55362-80-6 9-bromononan-1-ol 

Downstream Products

• 405506-78-7 (2R,2'R,5'S,6'S)-12-(5'-hydroxy-6'-hydroxymethyl-1'-tosylpiperidin-2'-yl)dodecane-1,2-diol 
• 405506-76-5 (2S,3S,6R,4''R)-{6-[10'-(2'',2''-dimethyl-[1'',3'']dioxolan-4''-yl)decyl]-2-hydroxymethyl}-1-tosylpiperidin-3-ol 

Relevant academic research and scientific papers

A convenient route to alkaloid lipids: Application for the synthesis of a leptophylline A analogue

A synthetic route for efficient access to alkaloid lipids, using the chiral 2,3,6-trisubstituted piperidine acetaldehyde 9 as an intermediate, is reported. The utility of the synthetic route was demonstrated in the asymmetric synthesis of an unnatural analogue of Cassia leptophylla alkaloid lipid, leptophyllin A, in 16 steps and 15% overall yield starting from D-glucal.