SCOPUS 정보 검색 플랫폼

Volumn 365, Issue , 2013, Pages 61-68

Synthesis of ribo-hexopyranoside- and altrose-based azacrown ethers and their application in an asymmetric Michael addition

(6) Rapi, Zsolt a Bakó, Péter a Keglevich, György a Szöllsy, Áron b Drahos, László c Hegeds, László c

a BUDAPEST UNIVERSITY OF TECHNOLOGY AND ECONOMICS (Hungary)

b Department of Inorganic and Analytical Chemistry ^* (Hungary)

c INSTITUTE OF EXPERIMENTAL MEDICINE (Hungary)

Author keywords

Anhydro sugars; Asymmetric Michael addition; Enantioselectivity; Sugar based chiral crown ethers

Indexed keywords

AZACROWN ETHER; CATALYTIC CONDITIONS; CHIRAL CROWN ETHERS; ETHANOLAMINES; MICHAEL ADDITIONS; NITROSTYRENE; NUCLEOPHILIC REAGENT; PHASE TRANSFER; REGIOSELECTIVE RING OPENING;

ADDITION REACTIONS; ENANTIOSELECTIVITY; ETHERS; LIGANDS; SUGARS;

CROWN ETHERS;

ALTROSE; CARBOHYDRATE DERIVATIVE; CROWN ETHER DERIVATIVE; NUCLEOPHILE; PYRANOSIDE; RIBOHEXOPYRANOSIDE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC SYNTHESIS; CARBOHYDRATE SYNTHESIS; MICHAEL ADDITION; PRIORITY JOURNAL; RING OPENING;

BOROHYDRIDES; CATALYSIS; CHEMISTRY TECHNIQUES, SYNTHETIC; CHROMATOGRAPHY, LIQUID; CROWN ETHERS; HEXOSES; MAGNETIC RESONANCE SPECTROSCOPY; MALONATES; MOLECULAR STRUCTURE; PHASE TRANSITION; QUATERNARY AMMONIUM COMPOUNDS; STYRENES;

EID: 84870300134 PISSN: 00086215 EISSN: 1873426X Source Type: Journal
DOI: 10.1016/j.carres.2012.10.020 Document Type: Article

Times cited : (13)

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