141270-44-2

Upstream product

• 126380-43-6 [5-(1,3-dioxolan-2-yl)furan-2-yl]methanol 
• 188981-35-3 1,1-O,O-ethylidene-3,4-dideoxy-D,L-hex-3-enoz-2-ulopyranos-5-ulose 
• 141270-39-5 methyl 3,4-dideoxy-D,L-hex-3-enos-2-ulopyranosid-5-ulose ethylene acetal 
• 126380-42-5 5-acetoxymethylfurfural ethylene acetal 
• 10551-58-3 5-acetoxymethyl-2-furaldehyde 
• 51694-22-5 ortho-nitrophenyl selenocyanate 
• 126380-46-9 methyl 3,4-dideoxy-α-D,L-glycerohex-3-enos-2-ulopyranoside ethylene acetal 
• 126380-48-1 methyl 5-O-acetyl-3,4-dideoxy-β-D,L-glycerohex-3-enos-2-ulopyranoside ethylene acetal 
• 126380-48-1 methyl 5-O-acetyl-3,4-dideoxy-α-D,L-glycerohex-3-enos-2-ulopyranoside ethylene acetal 
• 126380-46-9 6-[1,3]Dioxolan-2-yl-6-methoxy-3,6-dihydro-2H-pyran-3-ol 
• 126380-46-9 (3R,6S)-6-[1,3]Dioxolan-2-yl-6-methoxy-3,6-dihydro-2H-pyran-3-ol 
• 126380-46-9 (3S,6S)-6-[1,3]Dioxolan-2-yl-6-methoxy-3,6-dihydro-2H-pyran-3-ol 

Relevant academic research and scientific papers

TOTAL SYNTHESIS OF PROTECTED FORM OF FUNGI METABOLITE CORTALCERONE

Synthesis of methyl 4,5-dideoxy-D,L-hex 4-enos-2-ulopyranosid-3-ulose ethylene acetal, derivative of first natural sugar with dihydropyranone moiety, from 5-acetoxymethylfurfural is described.

TOTAL SYNTHESIS OF PROTECTED FORM OF FUNGI METABOLITE CORTALCERONE

Synthesis of methyl 4,5-dideoxy-D,L-hex-4-enos-2-ulopyranosid-3-ulose ethylene acetal, derivative of the first natural sugar with dihydropyranone moiety, from 5-acetoxymethylfurfural is described.It was shown that 1,3-transposition of the allylic alcohol