This submission belongs to the session a. General Organic Synthesis of the event The 16th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Oct, 2012
Citation
Claudio Santi, Jacek Scianowski, Anita Antoszewska, Francesca Mangiavacchi, Lorenzo Di Schino, Eco-Friendly Selenium Catalyzed Oxidative Cyclizations, in Proceedings of The 16th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2012, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-16-01023
1. Dipartimento di Chimica e Tecnologia del Farmaco, Gruppo “Catalysis and Green Chemistry” Università di Perugia
2. Dept Chemistry Nicolau Copernicus University Torun
Abstract
The selenium catalyzed oxidation by hydrogen peroxides was achieved for the synthesis of epoxides1. Our group recently developed the stereoselective synthesis of anti-1,2-diols passing through an epoxide intermediate2 and involving a perselenenic acid as actual catalyst of the whole process. Here we report the cyclofunctionalization of beta,gamma- and gamma,delta unsaturated acids, and alcohols. The stereoselectivity has been investigated starting from substrates containing additional chiral center in the α position as well as optically pure catalysts. All the reactions were carried out using 4 equivalents of hydrogen peroxides (30%) and diselenides as precatalysts without any organic solvents. High regio- and stereo-selectivity were obtained for almost all the substrates but unfortunately using optically pure diselenides only moderated enantiomeric excesses were obtained. The reaction conditions present important eco-friendly features (on water conditions, room temperature and pressure), generally affording high yields. - References - 1) Garcìa-Marìn,H; van der Toorn, J. C.; Mayoral, J. A.; Garcìa, J. I. J. Mol. Catal 2011, 83-88 2) Santoro, S; Santi, C.; Sabatini, M.; Testaferri, L; Tiecco, M. Adv. Synth. Catal. 2008, 350, 2881-2884
Keywords
Selenium
Oxidation
lactones
tetrahydrofuranes
Green Chemistry
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