828914-55-2

Upstream product

• 33985-40-9 (3aR,4S,6R,6aR)-tetrahydro-6-methoxy-2,2-dimethylfuro-[3,4-d][1,3]dioxole-4-carbaldehyde 
• 29325-28-8 (3aR,4R,6R,6aR)-4-methoxy-2,2-dimethyl-6-vinyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxole 
• 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 
• 2595-05-3 Diacetone D-glucose 
• 828914-54-1 (1'R,2R,3R,4S,5S)-4-azido-2-(1'-hydroxy-2',2'-bis-phenylsulfanylethyl)-5-methoxy-tetrahydropyran-3-ol 
• 828914-85-8 (3aR,3bS,6S,7R,7aS,8aR)-7-Bromo-2,2-dimethyl-hexahydro-[1,3]dioxolo[4,5]furo[3,2-b]pyran-6-ol 
• 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 
• 828914-88-1 (3aR,3bR,7S,7aR,8aR)-7-Azido-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5]furo[3,2-b]pyran-6-one 

Downstream Products

• 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 
• 828914-61-0 [(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 

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

NOVEL 2,7-DIOXO-BICYCLO[4.3.0]NON-5-YL-UREA DERIVATIVES

The present invention relates to novel fungicidal 2,7-dioxo-bicyclo[4.3.0] non-5-yl-urea derivatives, to processes for their preparation and to certain intermediate chemicals used in those processes. It also relates to the use of the compounds as biocides, to compositions containing biocidally effective amounts of the compounds and to methods of combating pathogens using the compounds. The invention encompasses 2,7-dioxo-bicyclo[4.3.0]non-5-yl-urea derivatives of formula (I) wherein R is H or C1-6alkyl (for example, methyl), the RO group is cis- or trans- to the NH2CONH group, R1 is H, formyl, C1-8alkylcarbonyl, C3-8cycloalkylcarbonyl, or optionally substituted benzoyl, and X is a N-linked heterocyclic group of the formula (II) or of the formula (III), wherein R2 is H, C1-4alkyl (especially methyl) or halo, or of the formula (IV): The compounds of formula I possess useful plant protecting properties and may advantageously be employed in agricultural practice for controlling or preventing the infestation of plants by phytopathogenic microorganisms, especially fungi.