Pure Appl. Chem., 2006, Vol. 78, No. 2, pp. 435-440
http://dx.doi.org/10.1351/pac200678020435
Alkenyl- and aryl[2-(hydroxymethyl)phenyl]dimethylsilanes: Tetraorganosilanes for the practical cross-coupling reaction
CrossRef Cited-by Linking
- Ishiyama Tatsuo, Saiki Takeaki, Kishida Emi, Sasaki Ikuo, Ito Hajime, Miyaura Norio: Aromatic C–H silylation of arenes with 1-hydrosilatrane catalyzed by an iridium(i)/2,9-dimethylphenanthroline (dmphen) complex. Org. Biomol. Chem. 2013, 11, 8162. <http://dx.doi.org/10.1039/c3ob41623b>
- Bergueiro Julián, Montenegro Javier, Cambeiro Fermín, Saá Carlos, López Susana: Cross-Coupling Reactions of Organosilicon Compounds in the Stereocontrolled Synthesis of Retinoids. Chemistry A European Journal 2012, 18, 4401. <http://dx.doi.org/10.1002/chem.201103360>
- Rogalski Szymon, Żak Patrycja, Miętkiewski Miłosz, Dutkiewicz Michał, Fiedorow Ryszard, Maciejewski Hieronim, Pietraszuk Cezary, Śmiglak Marcin, Schubert Thomas J.S.: Efficient synthesis of E-1,2-bis(silyl)ethenes via ruthenium-catalyzed homocoupling of vinylsilanes carried out in ionic liquids. Applied Catalysis A: General 2012, 445-446, 261. <http://dx.doi.org/10.1016/j.apcata.2012.08.038>
- Onoe Masahiro, Baba Katsuaki, Kim Yoonjoo, Kita Yusuke, Tobisu Mamoru, Chatani Naoto: Rhodium-Catalyzed Carbon–Silicon Bond Activation for Synthesis of Benzosilole Derivatives. J. Am. Chem. Soc. 2012, 134, 19477. <http://dx.doi.org/10.1021/ja3096174>
- Sore Hannah F., Galloway Warren R. J. D., Spring David R.: Palladium-catalysed cross-coupling of organosilicon reagents. Chemical Society Review 2012, 41, 1845. <http://dx.doi.org/10.1039/c1cs15181a>
- Boehner Christine M., Frye Elizabeth C., O'Connell Kieron M. G., Galloway Warren R. J. D., Sore Hannah F., Dominguez Patricia Garcia, Norton David, Hulcoop David G., Owen Martin, Turner Gillian: Aryl-Aryl Bond Formation by the Fluoride-Free Cross-Coupling of Aryldisiloxanes with Aryl Bromides. Chemistry A European Journal 2011, 17, 13230. <http://dx.doi.org/10.1002/chem.201102285>
- Peñafiel Itziar, Pastor Isidro M., Yus Miguel, Esteruelas Miguel A., Oliván Montserrat, Oñate Enrique: (NHC)Palladium Complexes from Hydroxy-Functionalized Imidazolium Salts as Catalyst for the Microwave-Accelerated Fluorine-Free Hiyama Reaction. Eur J Org 2011, 2011, 7174. <http://dx.doi.org/10.1002/ejoc.201101110>
- Hudrlik Paul F., Hudrlik Anne M., Jeilani Yassin A.: Intramolecular nucleophilic attack at silicon in o-silylbenzyl alcohols. Generation of allyl and benzyl anion equivalents. Tedrahedron 2011, 67, 10089. <http://dx.doi.org/10.1016/j.tet.2011.09.127>
- Marcuccio Sebastian M., Epa Ruwan, Moslmani Maisa, Hughes Andrew B.: Improved Hiyama cross-coupling reactions using HOMSi® reagents: a novel application of a palladacycle. Tetrahedron Letters 2011, 52, 7178. <http://dx.doi.org/10.1016/j.tetlet.2011.10.126>
- Denmark Scott E., Liu Jack H.-C.: Kreuzkupplungen von Organosiliciumverbindungen in der Naturstoffsynthese. Angew Chem 2010, 122, 3040. <http://dx.doi.org/10.1002/ange.200905657>
- Seiser Tobias, Cramer Nicolai: Rhodium(I)-Catalyzed 1,4-Silicon Shift of Unactivated Silanes from Aryl to Alkyl: Enantioselective Synthesis of Indanol Derivatives. angew chemie 2010, 122, 10361. <http://dx.doi.org/10.1002/ange.201005399>
- Denmark Scott E., Liu Jack H.-C.: Silicon-Based Cross-Coupling Reactions in the Total Synthesis of Natural Products. Angew Chem Int Ed 2010, 49, 2978. <http://dx.doi.org/10.1002/anie.200905657>
- Seiser Tobias, Cramer Nicolai: Rhodium(I)-Catalyzed 1,4-Silicon Shift of Unactivated Silanes from Aryl to Alkyl: Enantioselective Synthesis of Indanol Derivatives. Angew Chem Int Ed 2010, 49, 10163. <http://dx.doi.org/10.1002/anie.201005399>
- Lesbani Aldes, Kondo Hitoshi, Yabusaki Yusuke, Nakai Misaki, Yamanoi Yoshinori, Nishihara Hiroshi: Integrated Palladium-Catalyzed Arylation of Heavier Group 14 Hydrides. Chem Eur J 2010, 16, 13519. <http://dx.doi.org/10.1002/chem.201001437>
- Denmark Scott E., Liu Jack Hung-Chang: Sequential Processes in Palladium-Catalyzed Silicon-Based Cross-Coupling. Isr J Chem 2010, 50, 577. <http://dx.doi.org/10.1002/ijch.201000036>
- Shirbin Steven J., Boughton Berin A., Zammit Steven C., Zanatta Shannon D., Marcuccio Sebastian M., Hutton Craig A., Williams Spencer J.: Copper-free palladium-catalyzed Sonogashira and Hiyama cross-couplings using aryl imidazol-1-ylsulfonates. Tetrahetron Lett 2010, 51, 2971. <http://dx.doi.org/10.1016/j.tetlet.2010.03.110>
- Mehta Vaibhav Pravinchandra, Sharma Anuj, Van der Eycken Erik: Palladium-Catalyzed Desulfitative CC Cross-Coupling Reaction of (Hetero)Aryl Thioesters and Thioethers with Arylsiloxanes. Adv Synth Catal 2008, 350, 2174. <http://dx.doi.org/10.1002/adsc.200800395>
- Lu Biao, Falck John R.: Efficient Iridium-Catalyzed CH Functionalization/Silylation of Heteroarenes. Angew Chem 2008, 120, 7618. <http://dx.doi.org/10.1002/ange.200802456>
- Lu Biao, Falck John R.: Efficient Iridium-Catalyzed CH Functionalization/Silylation of Heteroarenes. Angew Chem Int Ed 2008, 47, 7508. <http://dx.doi.org/10.1002/anie.200802456>
- Saito Nozomi, Yamazaki Tetsuro, Sato Yoshihiro: Nickel(0)-catalyzed diastereoselective three-component coupling of 1,3-dienes, aldehydes, and organometallic reagents: influence of organometallic reagents on diastereoselectivity. Tetrahetron Lett 2008, 49, 5073. <http://dx.doi.org/10.1016/j.tetlet.2008.06.033>
- Wrackmeyer Bernd, Kupcik Tomas, Tok Oleg L., Shahid Khadija, Kempe Rhett: Ionic 1,2,5-oxonia- and zwitterionic 1,2,5-oxasilaboratole derivatives. Synthesis and molecular structures. Appl Organometal Chem 2007, 21, 676. <http://dx.doi.org/10.1002/aoc.1223>
- Nakao Yoshiaki, Sahoo Akhila K., Imanaka Hidekazu, Yada Akira, Hiyama Tamejiro: Alkenyl- and Aryl[2-(hydroxymethyl)phenyl]-dimethylsilanes: Tetraorganosilanes for the Practical Cross-Coupling Reaction. ChemInform 2006, 37. <http://dx.doi.org/10.1002/chin.200630279>
- Yamanoi Yoshinori, Nishihara Hiroshi: Rhodium-catalyzed silylation of ortho-functionalized aryl halides with hydrosilanes. Tetrahetron Lett 2006, 47, 7157. <http://dx.doi.org/10.1016/j.tetlet.2006.08.001>