Effects of ring substituents on enantioselective recognition of amino alcohols and acids in uryl-based binol receptors

Tetrahedron

Volumn 64, Issue 33, 2008, Pages 7704-7708

  Nandhakumar, Raju ^a   Ryu, Jayoung ^a   Park, Hyunjung ^a   Tang, Lijun ^a   Choi, Sujung ^a   Kim, Kwan Mook ^a  

^a Department of Chemistry   (South Korea)

Author keywords

Electron withdrawing group effect; Stereoconversion; Stereoselective recognition

Indexed keywords

2 HYDROXY 2' (3 PHENYLURYLBENZYL) 1,1' BINAPHTHYL 3 CARBOXALDEHYDE; 2 METHOXYMETHOXY 2' HYDROXY 1,1' BINAPHTHYL 3 CARBOXALDEHYDE; ALCOHOL; ALCOHOL DERIVATIVE; ALDEHYDE; AMINO ACID; AMINOALCOHOL; BROMINE DERIVATIVE; IMINE; PHENYL GROUP; PHENYLURYLBENZYLBROMIDE;

ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; DERIVATIZATION; ELECTRON TRANSPORT; ENANTIOSELECTIVITY; HYDROGEN BOND; MOLECULAR RECOGNITION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 46149115357     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.06.029     Document Type: Article

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