76886-31-2

Upstream product

• 137946-46-4 3-<(benzyloxy)methyl>cyclohexene 
• 67-56-1 methanol 
• 138630-47-4 c-3-<(benzyloxy)methyl>-r-1,2-epoxycyclohexane 
• 138749-89-0 t-3-<(benzyloxy)methyl>-r-1,2-epoxycyclohexane 
• 138630-56-5 cis-2-<(benzyloxy)methyl>cyclohexanol 
• 195049-52-6 6-[(benzyloxy)methyl]-1,4-dioxaspiro[4.5]decane 
• 6651-36-1 1-(Trimethylsilyloxy)cyclohexene 
• 2749-70-4 bis(benzyloxy)methane 
• 3587-60-8 Benzyloxymethyl chloride 
• 102839-33-8 N-Cyclohex-1-enyl-N,N',N'-trimethyl-ethane-1,2-diamine 

Downstream Products

• 919482-22-7 2-[(Benzyloxy)Methyl]-1-[1-(phenylthio)cyclopropyl]cyclohexanol 
• 36359-51-0 (+/-)-trans-2-phenylcyclohexanemethanol 
• 294868-77-2 9-{[2-(benzyloxymethyl)-1-methylsulfonylcyclohexyl]methyl}-N⁶-benzoyladenine 
• 294868-76-1 9-{[2-(benzyloxymethyl)-1-hydroxycyclohexyl]methyl}-N⁶-benzoyladenine 
• 294868-68-1 9-{[2-(benzyloxymethyl)-1-hydroxycyclohexyl]methyl}adenine 
• 294868-80-7 9-{[2-(benzyloxymethyl)cyclohex-1-en-1-yl]methyl}adenine 
• 294868-78-3 9-{[3-(benzyloxymethyl)cyclohex-1-en-2-yl]methyl}adenine 
• 294868-66-9 4-(benzyloxymethyl)-1-oxaspiro[2,5]octane 
• 294868-58-9 1-(benzyloxymethyl)-2-methylenecyclohexane 

Relevant academic research and scientific papers

COMPOSITIONS AND METHODS FOR MODULATING FXR

The present invention relates to compounds of Formula (I), a stereoisomer, enantiomer, a pharmaceutically acceptable salt or an amino acid conjugate thereof; wherein variables are as defined herein; and their pharmaceutical compositions, which are useful as modulators of the activity of Farnesiod X receptors (FXR).

N-dihydroxyalkyl-substituted 2-oxo-imidazole derivatives

The invention provides the compounds represented by the formula (I) in which, R stands for a dihydroxy-substituted C1-C6 alkyl group, and Cy stands for an optionally substituted C6-C10 bi- or tri-cyclic aliphati

Regiochemical control of the ring opening of 1,2-epoxides by means of chelating processes. Part 14: Regioselectivity of the opening reactions with MeOH of remote O-substituted 1,2-epoxycyclohexanes under gas-phase operating conditions

The regiochemical behavior of cyclohexene oxides bearing a remote O-functionality was determined in the gas-phase in opening reactions with MeOH, using a gaseous acid (D3/+, C(n)H5/+, Me2F+

Regiochemical Control of the Ring-Opening of 1,2-Epoxides by Means of Chelating Processes. 2. Synthesis and Reactions of the cis- and trans-Oxides of 4-cyclohexene, 3-Cyclohexenemethanol, and Methyl 3-Cyclohexenecarboxylate

The synthesis of the diastereoisomeric epoxides cis-1b-d and trans-2b-d and the products of their ring-opening by various nucleophiles are described.The results of the ring-openings of the trans-epoxides 2b-d can be rationalized by combining stereoelectro

Polycyclic amines useful as cerebrovascular agents

A novel series of polycyclic amines, derivatives, methods of making the compounds, novel intermediates, compositions containing them, and methods for using them in the treatment and prevention of cerebrovascular disorders are disclosed.

TRIMETHYLSILYL TRIFLATE CATALYZED ALDOL-TYPE REACTION OF ENOL SILYL ETHERS AND ACETALS OR RELATED COMPOUNDS

Trimethylsilyl triflate with or without added hindered tertiary amines catalyzes directed condensation of enol trimethylsilyl ethers with acetals, orthoformate, or 2-acetoxytetrahydrofuran or -pyrans to give the corresponding β-alkoxy carbonyl compounds.R

TRIMETHYLSILYL TRIFLATE IN ORGANIC SYNTHESIS

Trimethylsilyl triflate is a powerful silylating agent for organic compounds and acts as a catalyst which accelerates a variety of nucleophilic reactions in aprotic media.The reactions proceed via one-center, electrophilic coordination of the silyl group to hetero functional groups and exhibit unique selectivities.

CONDENSATION OF ENOL SILYL ETHERS AND DIALKOXYMETHANES CATALYZED BY TRIMETHYLSILYL TRIFLUOROMETHANESULFONATE. REGIOSPECIFIC SYNTHESIS OF α-ALKOXYMETHYL KETONES

A facile, regiospecific entry to α-alkoxymethyl ketones is described.