94318-23-7

Upstream product

• 22668-89-9 N-(cyclohexylidene)-1-propanamine 
• 52853-20-0 benzylidene dimethyl ammonium chloride 
• 100-52-7 benzaldehyde 
• 104412-60-4 cyclohexen-1-yloxybis(dimethylamino)borane 
• 1125-99-1 1-(1-Cyclohexen-1-yl)pyrrolidine 
• 108-94-1 cyclohexanone 
• 124-40-3 dimethyl amine 

Downstream Products

• 300659-25-0 1-(2-chlorobenzyl)-2-(dimethylaminophenylmethyl)cyclohexanol, hydrochloride 
• 300659-29-4 1-(3-chlorobenzyl)-2-(dimethylaminophenylmethyl)cyclohexanol, hydrochloride 
• 300659-75-0 1-(3,4-difluorobenzyl)-2-(dimethylaminophenylmethyl)cyclohexanol, hydrochloride 
• 300659-37-4 2-(dimethylaminophenylmethyl)-1-(3-trifluoromethylbenzyl)cyclohexanol, hydrochloride 
• 300659-12-5 2-(dimethylaminophenylmethyl)-1-(2-fluorobenzyl)cyclohexanol, hydrochloride 
• 300660-01-9 2-(dimethylaminophenylmethyl)-1-(3-phenylpropyl)cyclohexanol, hydrochloride 
• 300659-65-8 1-(2,4-difluorobenzyl)-2-(dimethylaminophenylmethyl)cyclohexanol, hydrochloride 
• 300658-88-2 2-(dimethylaminophenylmethyl)-1-(3-methoxybenzyl)cyclohexanol, hydrochloride 
• 300658-76-8 2-(dimethylaminophenylmethyl)-1-(4-fluorophenyl)cyclohexanol, hydrochloride 
• 300659-14-7 2-(dimethylaminophenylmethyl)-1-(4-fluorobenzyl)cyclohexanol, hydrochloride 
• 300659-31-8 1-(2,4-dichlorobenzyl)-2-(dimethylaminophenylmethyl)cyclohexanol, hydrochloride 
• 300658-72-4 2-(dimethylaminophenylmethyl)-1-(4-methoxyphenyl)cyclohexanol, hydrochloride 
• 300659-63-6 2-(dimethylaminophenylmethyl)-1-(4-methoxybenzyl)cyclohexanol, hydrochloride 
• 300658-96-2 2-(dimethylaminophenylmethyl)-1-furan-3-ylcyclohexanol, hydrochloride 

Relevant academic research and scientific papers

A new look at boron enolate chemistry: Aminative C-C bond formation using diaminoboron enolate with aldehyde

Unlike ordinary boron enolates, such as dialkylboryl (R2B) and dialkoxyboryl ((RO)2B) derivatives, reactions of diaminoboryl ((R2N)2B) enolates with aldehydes proceed with the concurrent transfer of amino and enoxy groups from the boron to the aldehyde carbon, yielding β-amino ketones in a selective manner.

Use of substituted 4-amino-1-phenylbutan-2-ol compounds as medicaments

The invention relates to the use of substituted 4-amino-1-phenylbutan-2-ol compounds in the form of their racemates, enantiomers, diastereomers or corresponding bases or corresponding salts of physiologically acceptable acids as regulators for the nocicep

3-amino-3-arylpropan-1-ol-compounds, their preparation and use

3-amino-3-arylpropan-1-ol compounds corresponding to the formula I in which R1to R5, A and X have the meanings according to claim1, and their preparation and use as medicaments.

Regio- und diastereoselektive Synthese von β-Aminoketonen durch Addition von Iminen an Iminiumsalze

Keywords: Aminoalkylierungen; Asymmetrische Synthesen; Imine; Mannich-Basen

Diastereoselektive Synthese neuartiger Mannich-Basen mittels Titanderivaten

Trichlorotitanium dialkylamino-alkoxides (2; titanates of N,O-hemiacetals) are generated either from the corresponding lithium alkoxides and titanium tetrachloride (Scheme I) or by addition of trichloro-dialkylamino-titanium to aldehydes.The electrophilic