Pure Appl. Chem., 2007, Vol. 79, No. 11, pp. 1929-1938
http://dx.doi.org/10.1351/pac200779111929
Photochemistry in synthesis: Where, when, and why
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- Leseurre Lucie, Merea Cécilia, Duprat de Paule Sébastien, Pinchart Alain: Eco-footprint: a new tool for the “Made in Chimex” considered approach. Green Chem. 2014, 16, 1139. <http://dx.doi.org/10.1039/c3gc42201a>
- Eberhard Jens, Peuntinger Katrin, Rath Susann, Neumann Beate, Stammler Hans-Georg, Guldi Dirk M., Mattay Jochen: A study of acridine and acridinium-substituted bis(terpyridine)zinc(ii) and ruthenium(ii) complexes as photosensitizers for O2 (1Δg) generation. Photochem. Photobiol. Sci. 2014, 13, 380. <http://dx.doi.org/10.1039/c3pp50349f>
- Ribeiro Sónia, Serra Arménio C., A. Rocha Gonsalves António M. d': Efficient Solar Photooxygenation with Supported Porphyrins as Catalysts. ChemCatChem 2013, 5, 134. <http://dx.doi.org/10.1002/cctc.201200532>
- Socol Yehoshua: High-power free-electron lasers–technology and future applications. Optics & Laser Technology 2013, 46, 111. <http://dx.doi.org/10.1016/j.optlastec.2012.06.040>
- Ogawa Daisuke, Li Jing, Suetsugu Masato, Jiao Jiao, Iwasaki Masayuki, Nishihara Yasushi: Palladium-free synthesis of unsymmetrical diarylethynes by cross-coupling reaction of alkynylboronates with aryl iodides catalyzed by CuCl. Tetrahedron Letters 2013, 54, 518. <http://dx.doi.org/10.1016/j.tetlet.2012.11.069>
- Elvira Katherine S., Wootton Robert C. R., Reis Nuno M., Mackley Malcolm R., deMello Andrew J.: Through-Wall Mass Transport as a Modality for Safe Generation of Singlet Oxygen in Continuous Flows. ACS Sustainable Chem. Eng. 2013, 1, 209. <http://dx.doi.org/10.1021/sc300093j>
- Gassama Abdoulaye, Ernenwein Cédric, Youssef Ali, Agach Mickaël, Riguet Emmanuel, Marinković Siniša, Estrine Boris, Hoffmann Norbert: Sulfonated surfactants obtained from furfural. Green Chem. 2013, 15, 1558. <http://dx.doi.org/10.1039/c3gc00062a>
- Huang Cheng-mei, Jiang Heng, Wang Ru-zhi, Quah Ching Kheng, Fun Hoong-Kun, Zhang Yan: Photocycloadditions of substituted oxazoles with isoquinoline-1,3,4-trione—chemo-, regio-, diastereoselectivities and transformation of the photocycloadducts. Org. Biomol. Chem. 2013, 11, 5023. <http://dx.doi.org/10.1039/c3ob40645h>
- 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>
- 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>
- Samokhvalov Alexander: Desulfurization of Real and Model Liquid Fuels Using Light: Photocatalysis and Photochemistry. Catalysis Reviews 2012, 54, 281. <http://dx.doi.org/10.1080/01614940.2012.650958>
- Eissen Marco, Brinkmann Tobias, Klein Mieke, Schwartze Britta, Weiß Markus: Einsatz von Kennzahlen in frühen Phasen der Syntheseentwicklung - Zwei Fallstudien. Chem -Ing -Tech 2011, 83, 1597. <http://dx.doi.org/10.1002/cite.201100114>
- Jahjah Rabih, Gassama Abdoulaye, Dumur Frédéric, Marinković Siniša, Richert Sabine, Landgraf Stephan, Lebrun Aurélien, Cadiou Cyril, Sellès Patrice, Hoffmann Norbert: Photochemical Electron Transfer Mediated Addition of Naphthylamine Derivatives to Electron-Deficient Alkenes. J Org Chern 2011, 76, 7104. <http://dx.doi.org/10.1021/jo201080m>
- 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>
- Struble Justin R., Lee Suk Joong, Burke Martin D.: Ethynyl MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis. Tetrahedron 2010, 66, 4710. <http://dx.doi.org/10.1016/j.tet.2010.04.020>
- Wang Hongjuan, Sun Fengqiang, Zhang Yu, Li Laisheng, Chen Hongyu, Wu Qingsong, Yu Jimmy C.: Photochemical growth of nanoporous SnO2 at the air–water interface and its high photocatalytic activity. J Mater Chem 2010, 20, 5641. <http://dx.doi.org/10.1039/b926930d>
- Protti Stefano, Dondi Daniele, Fagnoni Maurizio, Albini Angelo: Assessing photochemistry as a green synthetic method. Carbon–carbon bond forming reactions. Green Chem 2009, 11, 239. <http://dx.doi.org/10.1039/b810594d>
- Beach Evan S., Cui Zheng, Anastas Paul T.: Green Chemistry: A design framework for sustainability. Energy Environ Sci 2009, 2, 1038. <http://dx.doi.org/10.1039/b904997p>
- Han Xue, Bourne Richard A., Poliakoff Martyn, George Michael W.: Strategies for cleaner oxidations using photochemically generated singlet oxygen in supercritical carbon dioxide. Green Chem 2009, 11, 1787. <http://dx.doi.org/10.1039/b914074c>
- Eissen Marco, Lenoir Dieter: Electrophilic Bromination of Alkenes: Environmental, Health and Safety Aspects of New Alternative Methods. Chem Eur J 2008, 14, 9830. <http://dx.doi.org/10.1002/chem.200800462>
- Yoshimi Yasuharu, Ishise Akihiro, Oda Hiromu, Moriguchi Yousuke, Kanezaki Hiroki, Nakaya Yukari, Katsuno Kayoko, Itou Tatsuya, Inagaki Sho, Morita Toshio: Hydroxide ion as electron source for photochemical Birch-type reduction and photodehalogenation. Tetrahetron Lett 2008, 49, 3400. <http://dx.doi.org/10.1016/j.tetlet.2008.03.123>