258531-66-7

Upstream product

• 14086-08-9 (R)-2-(2-furyl)-1,2-ethanediol 
• 258531-65-6 (2S,6R)-2-(tert-Butyldiphenylsilyloxymethyl)-6-ethoxy-1-tosyl-1,6-dihydropyridin-3(2H)-one 
• 249928-45-8 (2S,6S)-2-(tert-Butyldiphenylsilyloxymethyl)-6-hydroxy-1-tosyl-1,6-dihydropyridin-3(2H)-one 
• 249928-44-7 (S)-1-(furan-2-yl)-2-tert-butyldiphenylsilyloxy-N-(toluene-4-sulfonyl)ethylamine 
• 258531-64-5 (S)-2-(tert-Butyldiphenylsilyloxy)-1-(2-furyl)ethyl azide 
• 124067-17-0 (2R) 1-<(t-butyldiphenylsilyl)oxy>-2-furanylethanol 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 405506-65-2 (2S,3S,6R)-3-benzyloxy-2-(tert-butyldiphenylsilyloxymethyl)-6-ethoxy-1-tosylpiperidine 
• 405506-74-3 (2S,3S,6S,4''R)-3-benzyloxy-2-(tert-butyldiphenylsilyloxymethyl)-6-[10'-(2'',2''-dimethyl-[1'',3'']dioxolan-4''-yl)dec-2'-enyl]-1-tosylpiperidine 
• 405506-75-4 (2S,3S,6S,4''R)-{3-benzyloxy-6-[10'-(2'',2''-dimethyl-[1'',3'']dioxolan-4''-yl)dec-2'-enyl]-1-tosylpiperidin-2-yl}methanol 
• 405506-67-4 (2S,3S,6R)-6-allyl-3-benzyloxy-2-(tert-butyldiphenylsilyloxymethyl)-1-tosylpiperidine 
• 405506-69-6 (2S,3S,6R)-[5-benzyloxy-6-(tert-butyldiphenylsilyloxymethyl)-1-tosylpiperidin-2-yl]acetaldehyde 
• 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 
• 405506-78-7 (2R,2'R,5'S,6'S)-12-(5'-hydroxy-6'-hydroxymethyl-1'-tosylpiperidin-2'-yl)dodecane-1,2-diol 

Relevant academic research and scientific papers

Transformation of D-glucal to (2S)-hydroxymethyl-dihydropyridones as intermediates to piperidine alkaloids

The efficient transformation of D-glucal to (2S)-hydroxymethyl- dihydropyridone 1 in five steps and 61% overall yield is reported. The latter is used as chiral building block for the synthesis of piperidine alkaloids. The preparation of piperidinol 8, whi