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Volumn 65, Issue 15, 2009, Pages 2927-2934
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The Vilsmeier reagent: a useful and versatile reagent for the synthesis of 2-azetidinones
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Author keywords
[No Author keywords available]
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Indexed keywords
(CHLOROMETHYLENE)DIMETHYLAMMONIUM CHLORIDE;
1 (4 ETHOXYPHENYL) 3 (5 NORBORNENE 2,3 DICARBOXYLOYLIMIDO) 4 (4 NITROPHENYL)AZETIDIN 2 ONE;
1 (4 ETHOXYPHENYL) 3 (NAPHTHALEN 2 YLOXY) 4 (4 NITROPHENYL)AZETIDIN 2 ONE;
1 (4 ETHOXYPHENYL) 3 METHOXY 4 (4 NITROPHENYL)AZETIDIN 2 ONE;
1 (4 ETHOXYPHENYL) 3 METHOXY 4 4 TOLYLAZETIDIN 2 ONE;
1 (4 ETHOXYPHENYL) 4 (4 METHOXYPHENYL) 3 PHENOXY AZETIDIN 2 ONE;
1 (4 ETHOXYPHENYL) 4 (4 NITROPHENYL) 3 PHENOXY AZETIDIN 2 ONE;
1 (4 ETHOXYPHENYL) 4 (4 NITROPHENYL) 3 VINYLAZETIDIN 2 ONE;
1 (4 METHOXYPHENYL) 3 (5 NORBORNENE 2,3 DICARBOXYLOYLIMIDO) 4 (4 NITROPHENYL)AZETIDIN 2 ONE;
1 (4 METHOXYPHENYL) 3 PHENOXY 4 4 TOLYLAZETIDIN 2 ONE;
1' BENZYL 1 (2,4 DIMETHOXYPHENYL) 3 PHENOXYSPIRO[AZETIDINE 2,3' INDOLINE] 2',4 DIONE;
1' BENZYL 3 (2,4 DICHLOROPHENOXY) 1 (2,4 DIMETHOXYPHENYL)SPIRO[AZETIDINE 2,3' INDOLINE] 2'4 DIONE;
1,4 BIS (4 METHOXYPHENYL) 3 VINYLAZETIDIN 2 ONE;
2 (1 (4 ETHOXYPHENYL) 2 (4 METHOXYPHENYL) 4 OXOAZETIDIN 3 YL)ISOINDOLINE 1,3 DIONE;
2 (1 (4 ETHOXYPHENYL) 2 (4 NITROPHENYL) 4 OXOAZETIDIN 3 YL)ISOINDOLINE 1,3 DIONE;
2 (1 (4 ETHOXYPHENYL) 2 OXO 4 4 TOLYLAZETIDIN 3 YL)ISOINDOLINE 1,3 DIONE;
2 (1 (4 METHOXYPHENYL) 2 OXO 4 STYRYLAZETIDIN 3 YL)ISOINDOLINE 1,3 DIONE;
2 [2 (3,4 DIMETHOXYPHENYL) 1 (4 METHOXYPHENYL) 4 OXOAZETIDIN 3 YL] 4 NITROISOINDOLE 1,3 DIONE;
2 AZETIDINONE DERIVATIVE;
3 (2,4 DICHLOROPHENOXY) 1 (4 ETHOXYPHENYL) 4 (4 NITROPHENYL)AZETIDIN 2 ONE;
4 (3,4 DIMETHOXYPHENYL) 1 (4 METHOXYPHENYL) 3 PHENOXY 2 AZETIDINONE;
4 (4 CHLOROPHENYL) 1 (4 ETHOXYPHENYL) 3 (NAPHTHALEN 2 YLOXY)AZETIDIN 2 ONE;
4 (4 CHLOROPHENYL) 1 (4 ETHOXYPHENYL) 3 PHENOXY AZETIDIN 2 ONE;
4 (4 CHLOROPHENYL) 1 (4 METHOXYPHENYL) 3 (5 NORBORNENE 2,3 DICARBOXYLOYLIMIDO)AZETIDIN 2 ONE;
4 (4 CHLOROPHENYL) 1 (4 METHOXYPHENYL) 3 PHENOXY AZETIDIN 2 ONE;
4 (4 CHLOROPHENYL) 1 (4 METHOXYPHENYL) 3 VINYLAZETIDIN 2 ONE;
4 (4 CHLOROPHENYL) 3 (2,4 DICHLOROPHENOXY) 1 (4 ETHOXYPHENYL)AZETIDIN 2 ONE;
BETA LACTAM DERIVATIVE;
CHLORIDE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ARTICLE;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
CYCLOADDITION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ONE POT SYNTHESIS;
PRIORITY JOURNAL;
STAUDINGER REACTION;
VILSMEIER HAACK REACTION;
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EID: 61549134853
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/j.tet.2009.02.005 Document Type: Article |
Times cited : (71)
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References (61)
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