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Volumn 62, Issue 10, 2006, Pages 2405-2412
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Synthesis of substituted 3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine as new scaffolds for potential bioactive compounds
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Author keywords
Halocarbonyl compounds; Protected 2 aminopyridine; Pyrido oxazines
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Indexed keywords
10 ACETYL 8,9,9A,10 TETRAHYDRO 7H PYRIDO[3,2 B]BENZO[1,4]OXAZIN 6 ONE;
2 ACETAMIDO 3 HYDROXYPYRIDINE;
2 CHLOROACRYLONITRILE;
2,4 DIACETYL 3,4 DIHYDRO 2H PYRIDO[3,2 B][1,4]OXAZINE;
2,4 DIACETYL 4H PYRIDO[3,2 B][1,4]OXAZINE;
4 ACETYL 2 BENZOYL 3,4 DIHYDRO 2H PYRIDO[3,2 B][1,4]OXAZINE;
4 ACETYL 3,4 DIHYDRO 2H PYRIDO[3,2 B][1,4]OXAZINE 2 CARBOXYLIC ACID ETHYL ESTER;
4 ACETYL 3,4 DIHYDRO 2H PYRIDO[3,2 B][1,4]OXAZINE 2 NITRILE;
4 ACETYL 4H PYRIDO[3,2 B][1,4]OXAZINE 2 CARBOXYLIC ACID METHYL ESTER;
4 ACETYL 4H PYRIDO[3,2 B][1,4]OXAZINE 2 NITRILE;
4 ACETYL 4H PYRIDO[3,2 B][1,4]OXAZINE 3 NITRILE;
4 ETHOXYCARBONYL 3,4 DIHYDRO 2H PYRIDO[3,2 B][1,4]OXAZINE 2 NITRILE;
4 TERT BUTYLCARBONYL 2,3 DIHYDRO 4H PYRIDO[3,2 B][1,4]OXAZINE 2 NITRILE;
CARBONYL DERIVATIVE;
ETHYL 2,3 DIBROMOPROPIONATE;
FUNCTIONAL GROUP;
HETEROCYCLIC COMPOUND;
METHYL 2,3 DIBROMOPROPIONATE;
OXAZINE DERIVATIVE;
PROPIONIC ACID DERIVATIVE;
PYRIDINE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
DRUG ACTIVITY;
DRUG POTENCY;
DRUG SYNTHESIS;
ISOMERISM;
POLYMERIZATION;
PRIORITY JOURNAL;
SUBSTITUTION REACTION;
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EID: 32444441663
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/j.tet.2005.11.071 Document Type: Article |
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Times cited : (13)
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References (27)
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