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Rümper, Jörg, Sokolov, Viktor V., Rauch, Karsten, Meijere, Armin De (1997) A New Efficient Synthesis of the Stilbenoid Laser Dyes BPS and Stilbene I by Palladium-Catalyzed Coupling of Ethene with Bromoarenes. Chemische Berichte, 130. 1193-1195 doi:10.1002/cber.19971300905

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Reference TypeJournal (article/letter/editorial)
TitleA New Efficient Synthesis of the Stilbenoid Laser Dyes BPS and Stilbene I by Palladium-Catalyzed Coupling of Ethene with Bromoarenes
JournalChemische Berichte
AuthorsRümper, JörgAuthor
Sokolov, Viktor V.Author
Rauch, KarstenAuthor
Meijere, Armin DeAuthor
Year1997 (September)Volume130
PublisherWiley
DOIdoi:10.1002/cber.19971300905Search in ResearchGate
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Mindat Ref. ID4334095Long-form Identifiermindat:1:5:4334095:4
GUID0
Full ReferenceRümper, Jörg, Sokolov, Viktor V., Rauch, Karsten, Meijere, Armin De (1997) A New Efficient Synthesis of the Stilbenoid Laser Dyes BPS and Stilbene I by Palladium-Catalyzed Coupling of Ethene with Bromoarenes. Chemische Berichte, 130. 1193-1195 doi:10.1002/cber.19971300905
Plain TextRümper, Jörg, Sokolov, Viktor V., Rauch, Karsten, Meijere, Armin De (1997) A New Efficient Synthesis of the Stilbenoid Laser Dyes BPS and Stilbene I by Palladium-Catalyzed Coupling of Ethene with Bromoarenes. Chemische Berichte, 130. 1193-1195 doi:10.1002/cber.19971300905
In(1997) Chemische Berichte Vol. 130. Wiley

See Also

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Albrecht, Karsten, Meijere, Armin De (1994) Palladium-Catalysed Multiple Coupling Reactions of β-Bromostyrene with Norbornene and Dicyclopentadiene. Chemische Berichte, 127. 2539-2541 doi:10.1002/cber.19941271229
König, Burkhard, Knieriem, Burkhard, Rauch, Karsten, Meijere, Armin De (1993) 4,5,12,13-Tetrabromo[2.2]paracyclophane – A New Bis(aryne) Equivalent. Chemische Berichte, 126. 2531-2534 doi:10.1002/cber.19931261130
Stulgies, Baldur, Prinz, Peter, Magull, Jörg, Rauch, Karsten, Meindl, Kathrin, Rühl, Stephan, de Meijere, Armin (2005) Six- and Eightfold Palladium-Catalyzed Cross-Coupling Reactions of Hexa- and Octabromoarenes. Chemistry - A European Journal, 11 (1). 308-320 doi:10.1002/chem.200400723
Untiedt, Sven, Meijere, Armin De (1994) New Cyclopropyl Building Blocks for Organic Synthesis, 28. Pd(0)-Catalysed Coupling of Cyclopropenylzinc Chlorides and Cyclopropenylstannanes — A New Efficient Synthesis of 1-Phenyl-, 1-Ethenyl-, and 1-Ethynyl-1-cyclopropenes. Chemische Berichte, 127. 1511-1515 doi:10.1002/cber.19941270826
Dyker, Gerlad, Siemsen, Peter, Sostmann, Stefan, Wiegand, Anke, Dix, Ina, Jones, Peter G. (1997) Synthesis of Polycyclic Hydrocarbons by Palladium-Catalyzed Cross-Coupling Reactions of Vinylic Bromides with Diphenylacetylene. Chemische Berichte, 130. 261-265 doi:10.1002/cber.19971300220
Wessjohann, Ludger, Krass, Norbert, Yu, Dahai, Meijere, Armin De (1992) A New Versatile Synthesis of Ring-Substituted 2-Cyclopropylglycines and Related Amino Acids. Chemische Berichte, 125. 867-882 doi:10.1002/cber.19921250418
Weber, Walter, Behrens, Ulrich, de Meijere, Armin (1981) Unprecedented reaction of 1,1′-bicyclopropylidene with tetrachlorocyclopropene. Chemische Berichte, 114. 1196-1199 doi:10.1002/cber.19811140339
König, Burkhard, Knieriem, Burkhard, Meijere, Armin De (1993) Double-Layered 1,4-Distyrylbenzene Chromophores–Synthesis, UV and Fluorescene Spectra. Chemische Berichte, 126. 1643-1650 doi:10.1002/cber.19931260723
Puls, Carsten, Stolle, Andreas, Meijere, Armin De (1993) Preparation and Properties of New Methano-Bridged Dibenzo[c,g]phenanthrenes. Chemische Berichte, 126. 1635-1641 doi:10.1002/cber.19931260722
Funke, Frank, Duetsch, Michael, Stein, Frank, Noltemeyer, Matthias, Meijere, Armin De (1994) Michael Addition of Imines to Alkynylcarbene Complexes with Subsequent Intramolecular Cyclization - An Efficient Three-Step Synthesis of 2H-Pyrroles. Chemische Berichte, 127. 911-920 doi:10.1002/cber.19941270520
König, Burkhard, Meijere, Armin De (1992) Synthesis and Diels-Alder Reactions of 1,2-Dimethylene- and 1,2,9,10-Tetramethylene[2.2]paracyclophane: New Routes to Bridge-Anellated [2.2]Paracyclophanedienes. Chemische Berichte, 125. 1895-1898 doi:10.1002/cber.19921250817
 
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