66574-19-4

Usage

InChI:InChI=1/C11H15NO/c1-9-11(13-8-12(9)2)10-6-4-3-5-7-10/h3-7,9,11H,8H2,1-2H3

Upstream product

• 50-00-0 formaldehyd 
• 90-82-4 rac-pseudoephedrine 
• 90-81-3 ephedrine 
• 90-82-4 pseudoephedrine 
• 75-09-2 dichloromethane 
• 74-95-3 1,1-dibromomethane 
• 1047392-28-8 methyl 2-(N-acetylamino)-5-ethynylbenzoate 

Downstream Products

• 462871-59-6 {[((1S,2S)-2-Chloro-1-methyl-2-phenyl-ethyl)-methyl-amino]-methyl}-phosphonic acid diethyl ester 
• 462871-75-6 ((2S,3R,4S)-1,4-Dimethyl-3-phenyl-azetidin-2-yl)-phosphonic acid diethyl ester 
• 462871-44-9 {[((1S,2S)-2-Hydroxy-1-methyl-2-phenyl-ethyl)-methyl-amino]-methyl}-phosphonic acid diethyl ester 
• 1201-56-5 (1S,2S)-N-Methylpseudoephedrine 

Relevant academic research and scientific papers

Study of alkaloids of the Siberian and Altai flora 14. Synthesis of alkaloid-based tertiary N-(3-arylprop-2-ynyl)amines

3-Arylprop-2-ynylamines containing the key fragment of known alkaloids of the Altai flora were synthesized by the Sonogashira and Mannich reactions.

1,2-Aminothioethers Derived from Ephedrine and Pseudoephedrine: Heterobidentate Ligands for the Palladium-Catalysed Asymmetric Allylic Substitution Reaction

Heterobidentate sulfide-tertiary amine ligands incorporating 1,2-aminothioethers derived from ephedrine and pseudoephedrine have been prepared and used successfully in the palladium-catalysed asymmetric allylic substitution reaction, giving ees of up to 89 percent. The stereoelectronic effects operating in the reactions are discussed.

An efficient asymmetric synthesis of azetidine 2-phosphonic acids

Substituted azetidinic 2-phosphonates were prepared in diastereoisomerically and enantiomerically pure form, starting from readily available β-amino alcohols. This synthesis involved a three-step sequence: (i) N-alkylation of the starting amino alcohol wi

Reaction of 3-methylamino-1,2-diols with dihalomethanes. Synthesis of chiral 4-substituted 3-methyltetrahydro-1,3-oxazin-5-ols

Enantiomerically pure 4,5-disubstituted 3-methyltetrahydro-1,3-oxazines have been obtained by reaction of 3-methylamino-1,2-diols with dichloromethane by regioselective differentiation of hydroxyl groups. (C) 2000 Published by Elsevier Science Ltd.

The solid-state diastereoselective formation of oxazolidines

A number of organic and organometallic aldehydes have been converted into optically active oxazolidines by solid-state interaction with (-)-ephedrine and (+)-pseudoephedrine. The stereoselectivity of the solid-state reaction is compared with that in boili