Indexed keywords
ARYLBORONIC ACIDS;
BIARYLS;
CYCLIZATIONS;
ENOL TRIFLATES;
FLUORENONES;
FRIEDEL-CRAFTS ACYLATION;
FUNCTIONALIZED;
SILYL ENOL ETHERS;
SUZUKI CROSS-COUPLING REACTIONS;
TARGET MOLECULES;
ACYLATION;
CYCLIZATION;
ETHERS;
ORGANIC COMPOUNDS;
REGIOSELECTIVITY;
SILANES;
BENZOPHENONE DERIVATIVE;
CARBOXYLIC ACID DERIVATIVE;
CYCLOPENTA[DEF]PHENANTHREN 4 ONE DERIVATIVE;
FLUORENONE DERIVATIVE;
METHYL 2 (4 METHOXYPHENYL) 4 METHYL 5,6,7,8 TETRAHYDRONAPHTHALENE 1 CARBOXYLATE;
METHYL 3,4',5 TRIMETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 3,4,4',5 TETRAMETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 3,4,5 TRIMETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 3,5 DIETHYL 3',4',5' TRIMETHOXYBIPHENYL 2 CARBOXYLATE;
METHYL 3,5 DIETHYL 4' METHOXYBIPHENYL 2 CARBOXYLATE;
METHYL 3,5 DIETHYL 4' METHYLBIPHENYL 2 CARBOXYLATE;
METHYL 3,5 DIETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 3,5 DIMETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 4 CHLORO 3,5 DIMETHYL 4' (TRIFLUOROMETHYL)BIPHENYL 2 CARBOXYLATE;
METHYL 4 CHLORO 3,5 DIMETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 4 CHLORO 4' METHOXY 3,5 DIMETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 4 ETHYL 3,4',5 TRIMETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 4 ETHYL 3,5 DIMETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 4 ETHYL 4' METHOXY 3,5 DIMETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 4 METHOXY 5' METHYL 1,1';3',1'' TERPHENYL 2' CARBOXYLATE;
METHYL 4 METHYL 2 (4 TOLYL) 5,6,7,8 TETRAHYDRONAPHTHALENE 1 CARBOXYLATE;
METHYL 4 METHYL 2 PHENYL 5,6,7,8 TETRAHYDRONAPHTHALENE 1 CARBOXYLATE;
METHYL 4' METHOXY 3,4,5 TRIMETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 4' METHOXY 3,5 DIMETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 4,4' DICHLORO 3,5 DIMETHYLBIPHENYL 2 CARBOXYLATE;
METHYL 4,5' DIMETHYL 1,1';3',1'' TERPHENYL 2' CARBOXYLATE;
METHYL 5' METHYL 1,1';3',1'' TERPHENYL 2' CARBOXYLATE;
METHYL 6 ETHYL 4' METHOXY 3,4,5 TRIMETHYLBIPHENYL 2 CARBOXYLATE;
PHENANTHRENE DERIVATIVE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
CONFERENCE PAPER;
CRYSTAL STRUCTURE;
CYCLIZATION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
FRIEDEL CRAFTS REACTION;
POLYMERIZATION;
SUZUKI REACTION;
1
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An isolated example of this method has been previously reported by Chan: see ref. 14a. During the synthesis of chlorinated and fluorinated arenes, we have recently reported the synthesis of fluorenones: (a) Hussain, I, Yawer, M. A, Lau, M, Pundt, T, Fischer, C, Reinke, H, Gorls, H, Langer, P. Eur. J. Org. Chem. 2008, 503
An isolated example of this method has been previously reported by Chan: see ref. 14a. During the synthesis of chlorinated and fluorinated arenes, we have recently reported the synthesis of fluorenones: (a) Hussain, I.; Yawer, M. A.; Lau, M.; Pundt, T.; Fischer, C.; Reinke, H.; Gorls, H.; Langer, P. Eur. J. Org. Chem. 2008, 503.
29
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CCDC 626089 and CCDC 698467 contain the crystallographic details of 7b and 7ab. These data are available free of charge at www.ccdc.cam.ac.uk/conts/ retrieving.html or can be ordered from the following address: Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; Fax: +44(1223)336033, or deposit@ccdc.cam.ac.uk.
CCDC 626089 and CCDC 698467 contain the crystallographic details of 7b and 7ab. These data are available free of charge at www.ccdc.cam.ac.uk/conts/ retrieving.html or can be ordered from the following address: Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; Fax: +44(1223)336033, or deposit@ccdc.cam.ac.uk.