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1-(1-naphthyl)ethylamine

Known as: 1-NAETAM, 1-Naphthalenemethanamine, alpha-methyl- 
National Institutes of Health

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Related topics

2 relations

Broader (2)

EthylaminesNaphthalenes

Papers overview

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2018
2018
Effective Guest Inclusion by a 6-O-Modified β-Cyclodextrin Dimer in Organic Solvents.
A 6-O-tert-butyldimethylsilylated β-cyclodextrin (TBDMS-β-CD) dimer, in which two TBDMS-β-CD rings are connected in a head-to… 
2015
2015
A novel method for the preparation of a chiral stationary phase containing an enantiopure acridino-18-crown-6 ether selector.
This paper reports a novel method for the preparation of chiral stationary phases (CSPs) using an acridino-18-crown-6 ether… 
2013
2013
Adsorption of 1-(1-naphthyl)ethylamine from solution onto platinum surfaces: implications for the chiral modification of heterogeneous catalysts.
2008
2008
1-(1-Naphthyl)ethylamine adsorption on platinum surfaces: on the mechanism of chiral modification in catalysis.
The adsorption of 1-(1-naphthyl)ethylamine (NEA) on platinum surfaces has been characterized by reflection-absorption infrared… 
2007
2007
Method for preparing optical pure 1-(1-naphthyl)ethylamine by separation
The invention relates to a method for preparing 1-(1-naphtaline) ethylamine possessing optical activity, which mainly solves… 
2001
2001
Mechanistic study of enantiomeric recognition of primary amino compounds using an achiral crown ether with cyclodextrin by capillary electrophoresis and nuclear magnetic resonance.
2000
2000
A novel chiral stationary phase in HPLC: optical resolution of racemic amino compounds by (1-->6)-2,5-anhydro-3,4-di-O-ethyl-D-glucitol bound on silica gel.
[(1-->6)-2,5-Anhydro-3,4-di-O-ethyl-D-glucitol]-bound silica gel (CSP 4a), which was prepared by a two-step reaction, was used as… 
1999
1999
α-Chymotrypsin-catalyzed enantioselective amidation of chiral amines using an N-protected amino acid carbamoylmethyl ester as acyl donor
Abstractα-Chymotrypsin catalyzed the highly enantioselective amidation of chiral amines such as 1-(1-naphthyl)ethylamine using N… 
1998
1998
Chiral recognition at the heme active site of nitric oxide synthase is markedly enhanced by L-arginine and 5,6,7,8-tetrahydrobiopterin.
The effects of substrate, L-Arg and cofactors, (6R)-L-erythro-5,6,7,8-tetrahydrobiopterin (H4B) and calmodulin (CaM), on chiral… 
Highly Cited
1992
Highly Cited
1992
Enzymatic resolution of racemic amines in a continuous reactor in organic solvents
An enzymatic process has been developed for the continuous production of the pharmaceutically important intermediate (R)‐1… 
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