CrossRef enabled

PAC Archives

Archive →

Pure Appl. Chem., 2007, Vol. 79, No. 11, pp. 1959-1968

http://dx.doi.org/10.1351/pac200779111959

Recent progress on photoreactions in microreactors

Yoshihisa Matsushita1, Teijiro Ichimura2, Nobuko Ohba2, Shinji Kumada2, Kosaku Sakeda2, Tadashi Suzuki2, Hideki Tanibata3 and Toshiaki Murata4

1 Department of Chemistry, Tokyo Institute of Technology, 2-12-1 Ohokayama, Meguro, Tokyo 152-8551, Japan
2 Department of Chemistry and Materials Science, Tokyo Institute of Technology, 2-12-1 Ohokayama, Meguro, Tokyo 152-8551, Japan
3 Mitsui Engineering & Shipbuilding Co., Ltd., Tokyo, Japan
4 Mitsui Zosen Plant Engineering Inc., Tokyo, Japan

CrossRef Cited-by theme picture

CrossRef Cited-by Linking

  • Hoffmann Norbert: Photochemical reactions applied to the synthesis of helicenes and helicene-like compounds. Journal of Photochemistry and Photobiology C: Photochemistry Reviews 2014, 19, 1. <http://dx.doi.org/10.1016/j.jphotochemrev.2013.11.001>
  • Wang Ning, Zhang Xuming, Wang Yu, Yu Weixing, Chan Helen L. W.: Microfluidic reactors for photocatalytic water purification. Lab Chip 2014, 14, 1074. <http://dx.doi.org/10.1039/c3lc51233a>
  • Maeda Hajime, Nashihara Satoshi, Mukae Hirofumi, Yoshimi Yasuharu, Mizuno Kazuhiko: Improved efficiency and product selectivity in the photo-Claisen-type rearrangement of an aryl naphthylmethyl ether using a microreactor/flow system. Res Chem Intermed 2013, 39, 301. <http://dx.doi.org/10.1007/s11164-012-0650-6>
  • Aillet Tristan, Loubiere Karine, Dechy-Cabaret Odile, Prat Laurent: Photochemical synthesis of a “cage” compound in a microreactor: Rigorous comparison with a batch photoreactor. Chemical Engineering and Processing: Process Intensification 2013, 64, 38. <http://dx.doi.org/10.1016/j.cep.2012.10.017>
  • Krivec Matic, Žagar Kristina, Suhadolnik Luka, Čeh Miran, Dražić Goran: Highly Efficient TiO2-Based Microreactor for Photocatalytic Applications. ACS Appl. Mater. Interfaces 2013, 5, 9088. <http://dx.doi.org/10.1021/am402389t>
  • Asano Keisuke, Uesugi Yuki, Yoshida Jun-ichi: Pauson–Khand Reactions in a Photochemical Flow Microreactor. Org. Lett. 2013, 15, 2398. <http://dx.doi.org/10.1021/ol4008519>
  • Liao Hsuan-Hung, Hsiao Chien-Chi, Sugiono Erli, Rueping Magnus: Shedding light on Brønsted acid catalysis – a photocyclization–reduction reaction for the asymmetric synthesis of tetrahydroquinolines from aminochalcones in batch and flow. Chem. Commun. 2013, 49, 7953. <http://dx.doi.org/10.1039/c3cc43996h>
  • Wegner Jens, Ceylan Sascha, Kirschning Andreas: Flow Chemistry - A Key Enabling Technology for (Multistep) Organic Synthesis. Adv. Synth. Catal. 2012, 354, 17. <http://dx.doi.org/10.1002/adsc.201100584>
  • Oelgemoeller M.: Highlights of Photochemical Reactions in Microflow Reactors. Chem. Eng. Technol. 2012, 35, 1144. <http://dx.doi.org/10.1002/ceat.201200009>
  • Hoffmann Norbert: Homogeneous Photocatalytic Reactions with Organometallic and Coordination Compounds-Perspectives for Sustainable Chemistry. ChemSusChem 2012, 5, 352. <http://dx.doi.org/10.1002/cssc.201100286>
  • Hosseinnia Azarmidokht, Keyanpour-Rad Mansoor: New approaches to photocatalytic reaction of low concentrations of arylamines in alcohols. Res Chem Intermed 2012, 38, 1411. <http://dx.doi.org/10.1007/s11164-011-0472-y>
  • Aida Shin, Terao Kimitada, Nishiyama Yasuhiro, Kakiuchi Kiyomi, Oelgemöller Michael: Microflow photochemistry—a reactor comparison study using the photochemical synthesis of terebic acid as a model reaction. Tetrahedron Letters 2012, 53, 5578. <http://dx.doi.org/10.1016/j.tetlet.2012.07.143>
  • Yavorskyy Alexander, Shvydkiv Oksana, Hoffmann Norbert, Nolan Kieran, Oelgemöller Michael: Parallel Microflow Photochemistry: Process Optimization, Scale-up, and Library Synthesis. Org. Lett. 2012, 14, 4342. <http://dx.doi.org/10.1021/ol301773r>
  • Lumley Emily K., Dyer Charlotte E., Pamme Nicole, Boyle Ross W.: Comparison of Photo-oxidation Reactions in Batch and a New Photosensitizer-Immobilized Microfluidic Device. Org. Lett. 2012, 14, 5724. <http://dx.doi.org/10.1021/ol3023424>
  • Shen Bo, Bedore Matthew W., Sniady Adam, Jamison Timothy F.: Continuous flow photocatalysis enhanced using an aluminum mirror: rapid and selective synthesis of 2′-deoxy and 2′,3′-dideoxynucleosides. Chem. Commun. 2012, 48, 7444. <http://dx.doi.org/10.1039/c2cc33356b>
  • Yavorskyy Alexander, Shvydkiv Oksana, Limburg Carolin, Nolan Kieran, Delauré Yan M. C., Oelgemöller Michael: Photooxygenations in a bubble column reactor. Green Chem 2012, 14, 888. <http://dx.doi.org/10.1039/c2gc16439f>
  • Fuse Shinichiro, Mifune Yuto, Tanabe Nobutake, Takahashi Takashi: Continuous-flow synthesis of activated vitamin D3 and its analogues. Org. Biomol. Chem. 2012, 10, 5205. <http://dx.doi.org/10.1039/c2ob25511a>
  • Hoffmann Norbert: Photochemical reactions of aromatic compounds and the concept of the photon as a traceless reagent. Photochem. Photobiol. Sci. 2012, 11, 1613. <http://dx.doi.org/10.1039/c2pp25074h>
  • van den Broek Sebastiaan A. M. W., Becker René, Koch Kaspar, Nieuwland Pieter J.: Microreactortechnology: Real-Time Flow Measurements in Organic Synthesis. Micromachines 2012, 3, 244. <http://dx.doi.org/10.3390/mi3020244>
  • Matsubara Hiroshi, Hino Yoshiko, Tokizane Masashi, Ryu Ilhyong: Microflow photo-radical chlorination of cycloalkanes. Chemical Engineering Journal 2011, 167, 567. <http://dx.doi.org/10.1016/j.cej.2010.08.086>
  • Yavorskyy Alexander, Shvydkiv Oksana, Nolan Kieran, Hoffmann Norbert, Oelgemöller Michael: Photosensitized addition of isopropanol to furanones in a continuous-flow dual capillary microreactor. Tetrahedron Letters 2011, 52, 278. <http://dx.doi.org/10.1016/j.tetlet.2010.11.018>
  • Ma Nan, Shi Wei, Zhang Ronghua, Zhu Zhiliang, Jiang Zhiqin: Study on improved diastereoselectivity in photo-induced electron transfer pinacol coupling reactions of substituted acetophenones. Tetrahetron Lett 2011, 52, 718. <http://dx.doi.org/10.1016/j.tetlet.2010.12.007>
  • Wegner Jens, Ceylan Sascha, Kirschning Andreas: Ten key issues in modern flow chemistry. Chem Commun 2011, 47, 4583. <http://dx.doi.org/10.1039/c0cc05060a>
  • Ravelli Davide, Protti Stefano, Neri Paolo, Fagnoni Maurizio, Albini Angelo: Photochemical technologies assessed: the case of rose oxide. Green Chem 2011, 13, 1876. <http://dx.doi.org/10.1039/c0gc00507j>
  • Shvydkiv Oksana, Yavorskyy Alexander, Tan Su Bee, Nolan Kieran, Hoffmann Norbert, Youssef Ali, Oelgemöller Michael: Microphotochemistry: a reactor comparison study using the photosensitized addition of isopropanol to furanones as a model reaction. Photochem Photobiol Sci 2011, 10, 1399. <http://dx.doi.org/10.1039/c1pp05024a>
  • Vesborg Peter C.K., Olsen Jakob L., Henriksen Toke R., Chorkendorff Ib, Hansen Ole: Gas-phase photocatalysis in μ-reactors. Chem Eng J 2010, 160, 738. <http://dx.doi.org/10.1016/j.cej.2010.03.083>
  • Gallagher Sonia, Hatoum Fadi, Zientek Nicolai, Oelgemöller Michael: Photodecarboxylative additions of N-protected α-amino acids to N-methylphthalimide. Tetrahetron Lett 2010, 51, 3639. <http://dx.doi.org/10.1016/j.tetlet.2010.05.020>
  • Belluau Vincent, Noeureuil Pierre, Ratzke Elfrun, Skvortsov Aleksei, Gallagher Sonia, Motti Cherri Ann, Oelgemöller Michael: Photodecarboxylative benzylations of phthalimide in pH 7 buffer: a simple access to 3-arylmethyleneisoindolin-1-ones. Tetrahetron Lett 2010, 51, 4738. <http://dx.doi.org/10.1016/j.tetlet.2010.07.017>
  • Fuse Shinichiro, Tanabe Nobutake, Yoshida Masahito, Yoshida Hayato, Doi Takayuki, Takahashi Takashi: Continuous-flow synthesis of vitamin D3. Chem Commun 2010, 46, 8722. <http://dx.doi.org/10.1039/c0cc02239j>
  • Shvydkiv Oksana, Yavorskyy Alexander, Nolan Kieran, Youssef Ali, Riguet Emmanuel, Hoffmann Norbert, Oelgemöller Michael: Photosensitized addition of isopropanol to furanones in a 365 nm UV-LED microchip. Photochem Photobiol Sci 2010, 9, 1601. <http://dx.doi.org/10.1039/c0pp00223b>
  • YE Mei-Ying, LI Bao-Xing, YE Rong-Min, LIU Jin-Hua: : Photodegradation of Organics with Titanium Oxide/Hydrogen Peroxide Catalyst System in Microreactor and Its Application in Environmental Analysis. CHINESE JOURNAL OF ANALYTICAL CHEMISTRY (CHINESE VERSION) 2010, 38, 643. <http://dx.doi.org/10.3724/SP.J.1096.2010.00643>
  • Sugimoto Atsushi, Fukuyama Takahide, Sumino Yukihito, Takagi Makoto, Ryu Ilhyong: Microflow photo-radical reaction using a compact light source: application to the Barton reaction leading to a key intermediate for myriceric acid A. Tetrahedron 2009, 65, 1593. <http://dx.doi.org/10.1016/j.tet.2008.12.063>
  • Hatoum Fadi, Gallagher Sonia, Baragwanath Louise, Lex Johann, Oelgemöller Michael: Photodecarboxylative benzylations of phthalimides. Tetrahetron Lett 2009, 50, 6335. <http://dx.doi.org/10.1016/j.tetlet.2009.08.115>
  • Hatoum Fadi, Gallagher Sonia, Oelgemöller Michael: Photodecarboxylative additions of phenoxyacetates to N-methylphthalimide. Tetrahetron Lett 2009, 50, 6593. <http://dx.doi.org/10.1016/j.tetlet.2009.09.067>
  • Murphy Brian, Goodrich Peter, Hardacre Christopher, Oelgemöller Michael: Green photochemistry: photo-Friedel–Crafts acylations of 1,4-naphthoquinone in room temperature ionic liquids. Green Chem 2009, 11, 1867. <http://dx.doi.org/10.1039/b913252j>
  • Matsushita Yoshihisa, Iwasawa Mayuko, Suzuki Tadashi, Ichimura Teijiro: Multiphase Photocatalytic Oxidation in a Microreactor. Chem Lett 2009, 38, 846. <http://dx.doi.org/10.1246/cl.2009.846>
  • Matsushita Yoshihisa, Ohba Nobuko, Suzuki Tadashi, Ichimura Teijiro: N-Alkylation of amines by photocatalytic reaction in a microreaction system. Catal Today 2008, 132, 153. <http://dx.doi.org/10.1016/j.cattod.2007.12.078>
  • Ouchi Akihiko, Sakai Hitoshi, Oishi Takeshi, Kaneda Masayuki, Suzuki Toshiaki, Saruwatari Atsushi, Obata Toru: Photochemical reduction of flavone with NaBH4 in batch and micro-channel reactors using excimer lasers. J Photochem Photobiol A Chem 2008, 199, 261. <http://dx.doi.org/10.1016/j.jphotochem.2008.05.024>
  • Coyle Emma E., Oelgemöller Michael: Micro-photochemistry: photochemistry in microstructured reactors. The new photochemistry of the future?. Photochem Photobiol Sci 2008, 7, 1313. <http://dx.doi.org/10.1039/b808778d>