864941-84-4

Upstream product

• 864941-67-3 (4R,4aR,7S,8R,8aR)-8-Azido-4-(bis-phenylsulfanyl-methyl)-2,2-dimethyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 
• 74-88-4 methyl iodide 
• 864941-68-4 (3aR,3bR,6R,7R,7aR,8aR)-7-azido-2,2-dimethyl-hexahydro-1,3,4,8-tetraoxa-cyclopenta[a]inden-6-ol 
• 828914-86-9 C₁₀H₁₄O₅ 
• 236425-24-4 (3aR,3bR,7aR,8aR)-2,2-dimethyl-3a,5,7a,8a-tetrahydro-3bH-1,3,4,8-tetraoxa-cyclopenta[a]indene 
• 236425-22-2 (3aR,5R,6R,6aR)-6-(allyloxy)-tetrahydro-2,2-dimethyl-5-vinylfuro[2,3-d][1,3]dioxole 
• 828914-84-7 C₁₄H₂₄O₁₀S₂ 
• 156742-37-9 (R)-1-[(3aR,5R,6R,6aR)-6-(allyloxy)-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxol-5-yl]ethane-1,2-diol 
• 33746-39-3 3-O-allyl-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 828914-90-5 (2R,3R,3bR,6S,7R,7aR)-7-azido-6-methoxy-2,2-dimethyl-hexahydro-[1,3]dioxolo[4,5]furo[3,2-b]pyran 
• 108-98-5 thiophenol 
• 864941-81-1 (3R,4R,5S)-4-Azido-3,5-dihydroxy-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 864941-66-2 (1R,2'R,3'R,4'R,5'S)-1-[4'-azido-3',5'-bis(tert-butyldimethylsilanyloxy)-tetrahydropyran-2'-yl]-2,2-bis-phenylsulfanyl-ethanol 
• 864941-64-0 (2R,3R,4R,5S)-4-azido-3,5-bis(tert-butyldimethylsilanyloxy)-tetrahydropyran-2-carboxylic acid methoxymethylamide 

Downstream Products

• 864941-60-6 (2R,3R,3aR,6S,7R,7aR)-7-azido-2-(6'-benzoylamino-purin-9'-yl)-6-methoxy-3-pivaloyloxy-hexahydrofuro[3,2-b]pyran 
• 828914-61-0 [(2R,3R,3aS,6S,7R,7aR)-3-hydroxy-2-(2',4'-dioxo-3',4'-dihydro-2H-pyrimidin-1'-yl)-6-methoxy-hexahydrofuro[3,2-b]pyran-7-yl]-urea 
• 828914-56-3 (2R,3R,3aR,6S,7R,7aR)-7-azido-hexahydro-6-methoxy-2-(phenylthio)-2H-furo[3,2-b]pyran-3-yl pivalate 
• 828914-55-2 (2R,3R,3aS,6S,7R,7aR)-7-azido-hexahydro-6-methoxy-2-(phenylthio)-2H-furo[3,2-b]pyran-3-ol 
• 828914-54-1 (1'R,2R,3R,4S,5S)-4-azido-2-(1'-hydroxy-2',2'-bis-phenylsulfanylethyl)-5-methoxy-tetrahydropyran-3-ol 

Relevant academic research and scientific papers

A scalable synthesis of 1-cytosinyl-N-malayamycin A: A potent fungicide

A stereocontrolled synthesis of 1-cytosinyl-N-malayamycin A, an N-analogue of the naturally occurring malayamycin A with fungicidal activity, is reported. The approach was designed to rely solely on substrate control for introduction of the required stere

Total synthesis of N-malayamycin A and related bicyclic purine and pyrimidine nucleosides

Methods are described for the total synthesis of bicyclic perhydrofuropyran nucleosides as N-analogues of the naturally occurring malayamycin A. Formation of the N-nucleosides relied on the activation of thioglycosides, proceeding via sulfonium intermedia