4380-71-6

Upstream product

• 16735-29-8 N-(1-oxo-1-phenylpropan-2-yl)benzamide 
• 154-41-6 norephedrine hydrochloride 
• 98-88-4 benzoyl chloride 
• 154-41-6 erythro-1-phenyl-1-hydroxy-2-propylammonium chloride 
• 38222-78-5 benzoic acid-((1RS,2SR)-2-amino-1-phenyl-propyl ester); hydrochloride 
• 67-56-1 methanol 
• 14838-15-4 u-2-amino-1-phenylpropan-1-ol 
• 38222-78-5 benzoic acid-((1RS,2RS)-2-amino-1-phenyl-propyl ester); hydrochloride 
• 492-41-1 (1R,2S)-norephedrine 
• 48115-38-4 norepinephrine 
• 16735-19-6 2-amino-1-phenylpropan-1-one hydrochloride 
• 100-52-7 benzaldehyde 
• 26251-08-1 2-nitro-1-phenylpropan-1-ol 
• 119-51-7 1-phenyl-1,2-propanedione 2-oxime 

Downstream Products

• 1630-31-5 cis-5-phenyl-4-methyl-1,3-thiazolidine-2-thione 
• 1592-59-2 threo-1-chloro-1-phenyl-2-propylammonium chloride 
• 1592-59-2 erythro-1-chloro-1-phenyl-2-propylammonium chloride 
• 154-41-6 threo-1-phenyl-1-hydroxy-2-propylammonium chloride 
• 78374-00-2 cis-5-phenyl-2-phenylamino-4-methyl-1,3-thiazoline 
• 78374-00-2 trans-5-phenyl-2-phenylamino-4-methyl-1,3-thiazoline 
• 78374-02-4 cis-2-diethylamino-5-phenyl-4-methyl-1,3-thiazoline 
• 78374-02-4 trans-2-diethylamino-5-phenyl-4-methyl-1,3-thiazoline 
• 78373-96-3 cis-5-phenyl-2-methoxy-4-methyl-1,3-thiazoline 
• 78373-96-3 trans-5-phenyl-2-methoxy-4-methyl-1,3-thiazoline 
• 78393-88-1 threo-1-chloro-1-phenyl-2-isothiocyanatopropane 
• 78393-88-1 erythro-1-chloro-1-phenyl-2-isothiocyanatopropane 
• 1630-31-5 trans-5-phenyl-4-methyl-1,3-thiazolidine-2-thione 
• 39861-30-8 2-chloro-1-methyl-2-phenyl-ethylamine; hydrochloride 

Relevant academic research and scientific papers

Process for the preparation of optically active amino alcohols

Process for preparing optically active β-amino alcohols represented by a general formula (2): Ra—C*H(OH)—C*H(Rb)—Rc wherein Ra and Rc are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, Rb is one member select

Stereoselective synthesis of 1,2-amino alcohols by asymmetric borane reduction of α-oxoketoxime ethers

Asymmetric reduction of α-oxoketoxime ethers with the reagents prepared in situ from trimethyl borate and chiral amino alcohols derived from either L-proline or α-pinene was investigated. Both cyclic and acyclic α- oxoketoxime ethers were reduced to afford the corresponding chiral 1,2amino alcohols with high enantioselectivities.

Ruthenium-catalyzed oxidations for selective syntheses of ketones and acyl cyanides. Selective acylation of amino compounds with acyl cyanides

Oxidation of alcohols to the corresponding carbonyl compounds with tert-butyl hydroperoxide in the presence of dichlorotris(triphenylphosphine)ruthenium catalyst gives the corresponding carbonyl compounds with high efficiency. This method can be applied to the oxidation of cyanohydrins to give acyl cyanides which are versatile synthetic intermediates. Acylation of amino compounds with acyl cyanides thus obtained proceeds chemoselectively. Thus, the reaction of amino alcohols with acyl cynides gives N-acylated products exclusively. In the similar N-acylation of polyamines primary amines are selectively acylated in the presence of secondary amines. These reactions are highly useful for the synthesis of spermidine and spermine alkaloids such as spermidine alkaloids such as spermidine siderophores. Dimeric cyclocoupling reaction of diacyl cyanides such as iso- and terephthaloyl cyanides with polyamines can be performed under the similar reaction conditions to give the corresponding polyazamacrocycles with high efficiency.

N-ALKYLOXAZABOROLIDINES DERIVED FROM EPHEDRINES

The synthesis of oxazaborolidines from amides derived from ephedrine and pseudoephedrine by treatment with BH3-THF is reported.The reaction affords chiral oxazaborolidines with nitrogen atom substituents of different steric requirements enlarging the pote

NON-CATALYTIC REDUCTION OF Α-OXIMINOKETONES AND Α-OXIMINOALCOHOLS TO ERYTHRO-2-AMINO-1-ARYLALKAN-1-OLS

A non-catalytic reduction of α-oximinoketones 1 and α-oximinoalcohols 2 to erythro-2-amino-1-arylalkan-1-ols 3 with lithium aluminium hydride is reported.The erythro-2-amino-1-arylalkan-1-ols are isolated as their hydrochlorides 5 and characterised as the erythro isomers by benzoylation.

STEREOCHEMICAL COURSE OF THE REACTION OF 2-HALOETHYL ISOTHIOCYANATES WITH NUCLEOPHILES. sTEREOSPECIFIC ROUTE TO 4,5-DISUBSTITUTED Δ2-THIAZOLINES AND THIAZOLIDINE-2-THIONES

Diastereoisomeric 1-chloro-1-phenyl-2-isothiocyanatopropanes have been prepared.They reacted stereospecifically with CH3ONa, diethylamine, aniline and NaSH to give pure cis or trans-4,5-disubstituted Δ2-thiazolines and thiazolidine-2-thiones whose configuration was determined using the nuclear Overhauser effect.The preponderant conformation of diastereoisomeric 1-chloro-1-phenyl-2-isothiocyanatopropanes was estimated on the basis of coupling constants of vicinal protons.