CrossRef enabled

PAC Archives

Archive →

Pure Appl. Chem., 2000, Vol. 72, No. 7, pp. 1321-1326

http://dx.doi.org/10.1351/pac200072071321

Environment-friendly organic synthesis. The photochemical approach

Angelo Albini, Maurizio Fagnoni and Mariella Mella

Department of Organic Chemistry, The University of Pavia, v. Taramelli 10, 27100 Pavia, Italy

CrossRef Cited-by theme picture

CrossRef Cited-by Linking

  • Kee Choon Wee, Chan Ke Min, Wong Ming Wah, Tan Choon-Hong: Selective Bromination of sp3 CH Bonds by Organophotoredox Catalysis. Asian Journal of Organic Chemistry 2013, n/a. <http://dx.doi.org/10.1002/ajoc.201300169>
  • Ronzani Filippo, Costarramone Nathalie, Blanc Sylvie, Benabbou Abdelhamid Khalil, Bechec Mickaël Le, Pigot Thierry, Oelgemöller Michael, Lacombe Sylvie: Visible-light photosensitized oxidation of α-terpinene using novel silica-supported sensitizers: Photooxygenation vs. photodehydrogenation. Journal of Catalysis 2013, 303, 164. <http://dx.doi.org/10.1016/j.jcat.2013.04.001>
  • Protti Stefano, Ravelli Davide, Fagnoni Maurizio, Albini Angelo: Smooth photogeneration of α,n-didehydrotoluenes (DHTs). Pure Appl. Chem. 2013, 1. <http://dx.doi.org/10.1351/PAC-CON-12-10-03>
  • Oelgemoeller M.: Highlights of Photochemical Reactions in Microflow Reactors. Chem. Eng. Technol. 2012, 35, 1144. <http://dx.doi.org/10.1002/ceat.201200009>
  • 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>
  • 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>
  • Protti Stefano, Fagnoni Maurizio, Monti Sandra, Réhault Julien, Poizat Olivier, Albini Angelo: Activation of aliphatic C–H bonds by tetracyanobenzene photosensitization. A time-resolved and steady-state investigation. RSC Adv 2012, 2, 1897. <http://dx.doi.org/10.1039/c2ra01054b>
  • Ravelli Davide, Montanaro Sara, Zema Michele, Fagnoni Maurizio, Albini Angelo: A Tin-Free, Radical Photocatalyzed Addition to Vinyl Sulfones. Synth Catal 2011, 353, 3295. <http://dx.doi.org/10.1002/adsc.201100591>
  • Sengupta Ananya, Chakraborty Indrajit, Ghosh Asitanga, Lahiri Saswati: Divergence in photoinduced electron transfer (PET) reactions: a useful strategy towards identifying route-selectivity in mixed ketones. Tetrahedron 2011, 67, 1689. <http://dx.doi.org/10.1016/j.tet.2010.12.064>
  • Galian R. E., Pérez-Prieto J.: Catalytic processes activated by light. Energy Environ Sci 2010, 3, 1488. <http://dx.doi.org/10.1039/c0ee00003e>
  • Dondi Daniele, Ravelli Davide, Fagnoni Maurizio, Mella Mariella, Molinari Alessandra, Maldotti Andrea, Albini Angelo: Regio- and Stereoselectivity in the Decatungstate Photocatalyzed Alkylation of Alkenes by Alkylcyclohexanes. Chem Eur J 2009, 15, 7949. <http://dx.doi.org/10.1002/chem.200900810>
  • 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>
  • Ng Danny, Yang Zhe, Garcia-Garibay Miguel A., Natarajan Arunkumar: Parallel Syntheses of (+)- and (−)-α-Cuparenone by Radical Combination in Crystalline Solids. Angew Chem 2007, 119, 6605. <http://dx.doi.org/10.1002/ange.200700679>
  • Natarajan Arunkumar, Ng Danny, Yang Zhe, Garcia-Garibay Miguel A.: Parallel Syntheses of (+)- and (−)-α-Cuparenone by Radical Combination in Crystalline Solids. Angew Chem Int Ed 2007, 46, 6485. <http://dx.doi.org/10.1002/anie.200700679>
  • Yadav Somnath, Banerjee Srirupa, Maji Dwijendralal, Lahiri Saswati: Synthesis of bicyclo[3.2.1]octanones via ketyl radical promoted rearrangements under reductive PET conditions. Tetrahedron 2007, 63, 10979. <http://dx.doi.org/10.1016/j.tet.2007.08.054>
  • Anastas Paul T., Beach Evan S.: Green chemistry: the emergence of a transformative framework. Green Chem Lett & Revs 2007, 1, 9. <http://dx.doi.org/10.1080/17518250701882441>
  • Dondi Daniele, Fagnoni Maurizio, Albini Angelo: Tetrabutylammonium Decatungstate-Photosensitized Alkylation of Electrophilic Alkenes: Convenient Functionalization of Aliphatic CH Bonds. Chem Eur J 2006, 12, 4153. <http://dx.doi.org/10.1002/chem.200501216>
  • Baciocchi Enrico, Bietti Massimo, Lanzalunga Osvaldo: Fragmentation reactions of radical cations. J Phys Org Chem 2006, 19, 467. <http://dx.doi.org/10.1002/poc.1096>
  • Suchard Oliver, Kane Ronan, Roe Bernard J., Zimmermann Elmar, Jung Christian, Waske Prashant A., Mattay Jochen, Oelgemöller Michael: Photooxygenations of 1-naphthols: an environmentally friendly access to 1,4-naphthoquinones. Tetrahedron 2006, 62, 1467. <http://dx.doi.org/10.1016/j.tet.2005.11.021>
  • Oelgem?ller Michael, Healy Niall, de Oliveira Lamark, Jung Christian, Mattay Jochen: Green photochemistry: solar-chemical synthesis of Juglone with medium concentrated sunlight. Green Chem 2006, 8, 831. <http://dx.doi.org/10.1039/b605906f>
  • Coskun Ali, Baytekin Bilge T., Akkaya Engin U.: Novel fluorescent chemosensor for anions via modulation of oxidative PET: a remarkable 25-fold enhancement of emission. Tetrahetron Lett 2003, 44, 5649. <http://dx.doi.org/10.1016/S0040-4039(03)01365-0>
  • Albini Angelo, Fagnoni Maurizio, Mella Mariella: ChemInform Abstract: Environment-friendly Organic Synthesis: The Photochemical Approach. ChemInform 2001, 32, no. <http://dx.doi.org/10.1002/chin.200116280>