33331-97-4

Upstream product

• 16302-35-5 4-methyl-3,6-dihydro-2H-pyran 

Downstream Products

• 133478-25-8 4-hydroxy-4-methyl-3-cyclohexylthiotetrahydropyran 
• 133478-23-6 (3R,4R)-4-Methyl-3-p-tolyloxy-tetrahydro-pyran-4-ol 
• 129673-36-5 ((3R,4R)-4-Hydroxy-4-methyl-tetrahydro-pyran-3-ylamino)-acetic acid 
• 133478-32-7 4-hydroxy-4-methyltetrahydropyran-3-yl benzoate 
• 134259-24-8 3-((3R,4R)-4-Hydroxy-4-methyl-tetrahydro-pyran-3-ylamino)-propionic acid 
• 134259-25-9 4-((3R,4R)-4-Hydroxy-4-methyl-tetrahydro-pyran-3-ylamino)-butyric acid 
• 133478-29-2 4-hydroxy-4-methyl-3-tetrahydropyranyl-cyclohexylsulfoxide 
• 133478-30-5 4-hydroxy-4-methyl-3-tetrahydropyranylcyclohexylsulfone 
• 84186-22-1 4-methyl-3-piperidinotetrahydropyran-4-ol p-nitrobenzoate 
• 90072-80-3 (3-Methyl-tetrahydro-furan-3-yl)-phenyl-methanol 
• 133478-22-5 4-hydroxy-4-methyl-3-phenoxytetrahydropyran 
• 129673-47-8 2-Benzoylamino-3-methyl-butyric acid (3S,4S)-4-hydroxy-4-methyl-tetrahydro-pyran-3-yl ester 
• 133478-36-1 S-(4-hydroxy-4-methyltetrahydropyran-3-yl)thiouronium sulfate 
• 16302-35-5 4-methyl-3,6-dihydro-2H-pyran 

Relevant academic research and scientific papers

Substituted alkenediols by alkylative double ring opening of dihydrofuran and dihydropyran epoxides

Equation presented Dihydrofuran and dihydropyran epoxides undergo alkylative double ring opening with organolithiums to provide a new route to substituted alkenediols.

Amino substituted dibenzothiophene derivatives for the treatment of disorders mediated by np y5 receptor

Compounds of formula (I): wherein: X is a group of formula (A) or (B): and R1, R2, R3, R4, n, x, y and z are as defined within are described. Processes for their preparation and their use in the treatment of disorders mediated by the neuropeptide Y5 receptor in a warm-blooded animal, such as a human being are also described.

Reaction of tetrahydropyranyl azides with 5-R-bicyclo[2.2.1]-2-heptenes

The reaction of 5-R-bicyclo[2.2.1]-2-heptenes with 3-azido-4-hydroxy-4-methyltetrahydropyran and 4-azidomethyl-4-hydroxytetrahydropyran, obtained by opening the oxirane ring in epoxytetrahydropyrans with sodium azide, leads to the formation of N-tetrahydropyranylaziridines with 100% stereoselectivity. 1998 Plenum Publishing Corporation.