228724-88-7

Upstream product

• 2978-10-1 O-benzyl-N,N'-diisopropylisourea 
• 228724-99-0 (2R,3aR,7aR)-Hexahydro-furo[3,2-b]pyran-2-carboxylic acid 
• 125877-98-7 (2'R,3'S)-<3'-(tert-butyldimethylsilyloxy)tetrahydropyran-2'-yl>ethanol 
• 125877-97-6 tert-Butyl-dimethyl-((2R,3S)-2-vinyl-tetrahydro-pyran-3-yloxy)-silane 
• 228724-94-5 (S)-(2R,3aR,7aR)-1-(Hexahydro-furo[3,2-b]pyran-2-yl)-ethane-1,2-diol 
• 228724-92-3 2-[(2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-yl]-ethanol 
• 228724-98-9 (E)-4-[(2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-yl]-but-2-en-1-ol 
• 228724-93-4 (E)-4-[(2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-yl]-but-2-enoic acid methyl ester 
• 228724-90-1 (2R,3S)-2-{2-[(4-Methoxy-phenyl)-diphenyl-methoxy]-ethyl}-tetrahydro-pyran-3-ol 
• 228724-91-2 (2R,3R)-2-{2-[(4-Methoxy-phenyl)-diphenyl-methoxy]-ethyl}-tetrahydro-pyran-3-ol 

Downstream Products

• 228725-02-8 (2S,3aR,7aR)-2-((S)-2-tert-Butoxycarbonylamino-2-methoxycarbonyl-ethyl)-hexahydro-furo[3,2-b]pyran-2-carboxylic acid benzyl ester 
• 228724-97-8 (2R,3aR,7aR)-2-((S)-2-tert-Butoxycarbonylamino-2-methoxycarbonyl-ethyl)-hexahydro-furo[3,2-b]pyran-2-carboxylic acid benzyl ester 
• 228724-96-7 (S)-4-((2R,3aR,7aR)-2-Benzyloxycarbonyl-hexahydro-furo[3,2-b]pyran-2-ylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 228725-01-7 (S)-4-((2S,3aR,7aR)-2-Benzyloxycarbonyl-hexahydro-furo[3,2-b]pyran-2-ylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 228724-95-6 (R)-4-[((2S,3aR,7aR)-2-Benzyloxycarbonyl-hexahydro-furo[3,2-b]pyran-2-yl)-hydroxy-methyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 228725-00-6 (R)-4-[((2R,3aR,7aR)-2-Benzyloxycarbonyl-hexahydro-furo[3,2-b]pyran-2-yl)-hydroxy-methyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Synthesis and biological activity of dysiherbaine model compound

Synthesis of dysiherbaine model compound 2 and its diastereomer 3 is described. The structurally simplified model compound 2, lacking the hydroxyl and N-methyl groups on the tetrahydropyran ring, induced convulsive behavior in mice upon intracerebral injections.