84025-82-1

Upstream product

• 634-03-7 trans-Phendimetrazine 
• 124368-83-8 (1R,2S)-(-)-2-Amino-1-phenyl-1-<(tert-butyldimethylsilyl)oxy>-propane 
• 89100-80-1 4-formyl-3-methyl-2-phenylmorpholine 
• 54804-28-3 (1RS,2SR)-2-(2-hydroxy-ethylamino)-1-phenyl-propan-1-ol 

Downstream Products

• 634-03-7 trans-Phendimetrazine 
• 83976-43-6 (2R,3S)-N-(1'-Cyclohexenyl)-3-methyl-2-phenylmorpholin 
• 84025-88-7 (+)-(2R,3S,6'S,1''R)-3-Methyl-N-<6'-(2''-nitro-1''-phenylaethyl)-1-cyclohexenyl>-2-phenylmorpholin 
• 83976-49-2 (-)-(2R,3S,6'R,1''S)-3-Methyl-N-<6'-(2''-nitro-1''-phenylaethyl)-1-cyclohexenyl>-2-phenylmorpholin 
• 95228-53-8 [2-(3,4-dimethoxy-phenyl)-1-methyl-ethyl]-(3t-methyl-2r-phenyl-morpholin-4-yl)-amine 
• 97297-07-9 (2-indol-3-yl-1-methyl-ethyl)-(3t-methyl-2r-phenyl-morpholin-4-yl)-amine 
• 97432-04-7 2-(3-methyl-2-phenyl-morpholin-4-ylamino)-1-phenyl-propan-1-ol 
• 98131-85-2 (3t-methyl-2r-phenyl-morpholin-4-yl)-(1,2,3,4-tetrahydro-naphthalen-1-yl)-amine 
• 98763-25-8 (1-furan-2-yl-ethyl)-(3t-methyl-2r-phenyl-morpholin-4-yl)-amine 
• 95555-40-1 (1-methyl-2-phenoxy-ethyl)-(3t-methyl-2r-phenyl-morpholin-4-yl)-amine 
• 94998-95-5 (3t-methyl-2r-phenyl-morpholin-4-yl)-(1-methyl-3-phenyl-propyl)-amine 
• 94436-89-2 (3t-methyl-2r-phenyl-morpholin-4-yl)-(1-phenyl-ethyl)-amine 
• 95558-62-6 (3t-methyl-2r-phenyl-morpholin-4-yl)-phenethyl-amine 
• 94681-96-6 (2-cyclohexyl-3-methyl-morpholin-4-yl)-(1-methyl-2-phenyl-ethyl)-amine 

Relevant academic research and scientific papers

Facile, efficient, and catalyst-free electrophilic aminoalkoxylation of olefins: Scope and application

A new one-pot electrophilic aminoalkoxylation reaction using olefin, cyclic ether, amine, and N-bromosuccinimide has been developed. The olefinic substrates and the cyclic ether partners can be flexibly varied to produce a range of amino ether derivatives. This novel protocol has been applied in the facile and efficient synthesis of biologically active morpholine compounds.

An approach to enantioselective 5-endo halo-lactonization reactions

Enantioselective lactonization of 4-substituted but-3-enoic acids using iodobis(N-methylephedrine) hexafluoroantimonate in dichloromethane at low temperatures is reported. The presence of bis(N-methylephedrine)silver(I) hexafluoroantimonate, derived from