Pure Appl. Chem., 2000, Vol. 72, No. 7, pp. 1327-1334
http://dx.doi.org/10.1351/pac200072071327
Free radicals in synthesis. Clean reagents affording oxidative or reductive termination
CrossRef Cited-by Linking
- Boto Alicia, Gallardo Juan A., Álvarez Eleuterio: One-Pot Conversion of Serine Derivatives and Amino Sugars into Oxazine Derivatives of γ-Aryl-γ-(hydroxy)amines. Eur J Org 2012, 2012, 391. <http://dx.doi.org/10.1002/ejoc.201101274>
- Boto Alicia, Hernández Dácil, Hernández Rosendo, Álvarez Eleuterio: Coupling Radical and Ionic Processes: An Unusual Rearrangement Affords Sugar and C-Glycoside Derivatives. Eur J Org Chem 2009, 2009, 3853. <http://dx.doi.org/10.1002/ejoc.200900427>
- Dichiarante Valentina, Fagnoni Maurizio, Albini Angelo: Eco-friendly hydrodehalogenation of electron-rich aryl chlorides and fluorides by photochemical reaction. Green Chem 2009, 11, 942. <http://dx.doi.org/10.1039/b904897a>
- 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>
- Francisco Cosme G., González Concepción C., Herrera Antonio J., Paz Nieves R., Suárez Ernesto: Chemoselective 1-ethylpiperidine hypophosphite (EPHP)-mediated intermolecular radical additions of 1-deoxy-1-halo-1-iodo-alditols to electron-deficient olefins. Tetrahetron Lett 2006, 47, 9057. <http://dx.doi.org/10.1016/j.tetlet.2006.10.086>
- Jahn Ullrich, Hartmann Philip, Kaasalainen Emmi: Efficient Oxidative Radical Cyclizations of Ester Enolates with Carbocation Desilylation as Termination: Synthesis of Cyclopentanoid Monoterpenes and Analogues†. Org Lett 2004, 6, 257. <http://dx.doi.org/10.1021/ol036233n>
- Bucher Götz, Winkler Michael, Wille Uta, Thiel Oliver R., Schalley Christoph A., Lindel Thomas: Organische Chemie 2001. Nachr Chem 2002, 50, 289. <http://dx.doi.org/10.1002/nadc.20020500308>
- Murphy John A.: ChemInform Abstract: Free Radicals in Synthesis: Clean Reagents Affording Oxidative or Reductive Termination. ChemInform 2001, 32, no. <http://dx.doi.org/10.1002/chin.200116279>
