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Volumn 57, Issue 15, 2001, Pages 3087-3098
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Stable annelated chiral NADH models with a rigidified amide part in the quinoline series: Synthesis, reactivity and grafting on a Merrifield resin
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Author keywords
Asymmetric reduction; Biomimetic NADH model; Grafting; Merrifield resins
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Indexed keywords
(1 HYDROXY 3 PHENYLPROP 2 YL) 2,3,4,5 TETRAHYDRO 8,9 DIMETHOXYAZEPINOL[4,3]QUINOLIN 1 ONE;
1,1 DIETHOXY 2 IODOETHANE;
2 (1 HYDROXY 3 PHENYLPROP 2 YL) 2,3,4,5 TETRAHYDRO 8 BENZYLO 9 METHOXYAZEPINO[4,3B]QUINOLIN 1 ONE;
2 (1 HYDROXY 3 PHENYLPROP 2 YL) 2,3,4,5 TETRAHYDRO 8 HYDROXY 9 METHOXYAZEPINO[4,3B]QUINOLIN 1 ONE;
2 (1 HYDROXY 3 PHENYLPROP 2 YL) 2,3,4,5 TETRAHYDRO 8,9 DIMETHOXY 6 METHYL 1 OXO AZEPINO [4,3B]QUINOLIN 1 ONE;
2 (1 HYDROXY 3 PHENYLPROP 2 YL) 2,3,4,5,6,11 HEXAHYDRO 8,9 DIMETHOXY 6 METHYLAZEPINO[4,3B]QUINOLIN 1 ONE;
2 (2 BENZYL 1 HYDROXYETHYL) 1 OXO 1,2,3,4 TETRAHYDROBENZO[1,3B]NAPHTHYRIDINE;
2 CHLOROQUINOLINE 3 CARBONITRILE;
2 ETHYLNYLQUINOLINE 3 CARBONITRILE;
3,4 DIMETHOXY 6 AMINOBENZALDEHYDE;
5 METHYL 2 (2 BENZYL 1 HYDROXYETHYL) 1 OXO 1,2,3,4,5,10 HEXAHYDROBENZO[1,6B]NAPHTHYRIDINE;
6 (4 TOLYAMINOMETHYLIDENE) 3 BENZYLOXY 4 METHOXY NITROBENZENE;
6 (4 TOLYAMINOMETHYLIDENE) 3,4 DIMETHOXYANILINE;
6 (4 TOLYAMINOMETHYLIDENE) 3,4 DIMETHOXYNITRO BENZENE;
6 (4 TOLYLAMINOMETHYLIDENE) 3 BENZYLOXY 4 METHOXYANILINE;
BENZENE DERIVATIVE;
ETHYL 2 (2 FORMYLETHYL) 6 METHOXY 7 BENZYLOXYQUINOLINE 3 CARBOXYLATE;
ETHYL 2 (2 FORMYLETHYL) 6,7 DIMETHOXYQUINOLINE 3 CARBOXYLATE;
ETHYL 2 [[N(1 HYDROXY 3 PHENYL)PROP 2 YL] 3 AMINOPROPYL] 6 METHOXY 7 BENZYLOXYQUINOLINE 3 CARBOXYLATE;
ETHYL 2,2 (3,3 DIETHOXYPROPYL) 6 METHOXY 7 BENZYL OXYQUINOLINE 3 CARBOXYLATE;
ETHYL 2,2 (3,3 DIETHOXYPROPYL) 6,7 DIMETHOXYQUINOLINE 3 CARBOXYLATE;
ETHYL 6,6 DIETHOXY 3 OXOHEXANOIC ACID;
ETHYL [[N(1 HYDROXY 3 PHENYL)PROP 2 YL]3 AMINOPROPYL] 6,7 DIMETHOXYQUINOLINE 3 CARBOXYLATE;
MAGNESIUM ION;
MANDELIC ACID DERIVATIVE;
MANDELIC ACID METHYL ESTER;
PHENYLGLYOXYLIC ACID METHYL ESTER;
QUINOLINE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
MODEL;
PRIORITY JOURNAL;
REACTION ANALYSIS;
STOICHIOMETRY;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
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EID: 0035831966
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/S0040-4020(01)00166-1 Document Type: Article |
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Times cited : (32)
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References (47)
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