{"_id":"acDZeiyzMEtXNquss","bibbaseid":"abdeslamakhatou-maryamrahimi-karimacheboub-longhosez-gilleshanquet-acidpromotedenantioselectiveoxygenatomtransferfromnalkylbinaphthylderivedoxaziridinesontosulfides-2007","author_short":["Abdeslam Akhatou","Maryam Rahimi","Karima Cheboub","Léon Ghosez","Gilles Hanquet"],"bibdata":{"bibtype":"article","type":"article","title":"Acid promoted enantioselective oxygen-atom transfer from N-alkyl binaphthyl-derived oxaziridines onto sulfides","volume":"63","issn":"0040-4020","url":"https://www.sciencedirect.com/science/article/pii/S0040402007003614","doi":"10.1016/j.tet.2007.02.119","abstract":"Acid-promoted asymmetric sulfoxidations of prochiral sulfides using binaphthyl-derived oxaziridines have been studied. The reactions of dialkyl or aryl-alkyl sulfides gave good yields of the corresponding sulfoxides with enantiopurities ranging from 20% to 80%. The influence of temperature and strength of the acid catalyst on enantioselectivity was studied. The absolute configuration of the resulting major enantiomer varied with the structure of the sulfide.","number":"27","journal":"Tetrahedron","author":[{"firstnames":[],"propositions":[],"lastnames":["Abdeslam Akhatou"],"suffixes":[]},{"firstnames":[],"propositions":[],"lastnames":["Maryam Rahimi"],"suffixes":[]},{"firstnames":[],"propositions":[],"lastnames":["Karima Cheboub"],"suffixes":[]},{"firstnames":[],"propositions":[],"lastnames":["Léon Ghosez"],"suffixes":[]},{"firstnames":[],"propositions":[],"lastnames":["Gilles Hanquet"],"suffixes":[]}],"month":"July","year":"2007","pages":"6232–6240","bibtex":"@article{abdeslam_akhatou_acid_2007,\n\ttitle = {Acid promoted enantioselective oxygen-atom transfer from {N}-alkyl binaphthyl-derived oxaziridines onto sulfides},\n\tvolume = {63},\n\tissn = {0040-4020},\n\turl = {https://www.sciencedirect.com/science/article/pii/S0040402007003614},\n\tdoi = {10.1016/j.tet.2007.02.119},\n\tabstract = {Acid-promoted asymmetric sulfoxidations of prochiral sulfides using binaphthyl-derived oxaziridines have been studied. The reactions of dialkyl or aryl-alkyl sulfides gave good yields of the corresponding sulfoxides with enantiopurities ranging from 20\\% to 80\\%. The influence of temperature and strength of the acid catalyst on enantioselectivity was studied. The absolute configuration of the resulting major enantiomer varied with the structure of the sulfide.},\n\tnumber = {27},\n\tjournal = {Tetrahedron},\n\tauthor = {{Abdeslam Akhatou} and {Maryam Rahimi} and {Karima Cheboub} and {Léon Ghosez} and {Gilles Hanquet}},\n\tmonth = jul,\n\tyear = {2007},\n\tpages = {6232--6240},\n}\n\n","author_short":["Abdeslam Akhatou","Maryam Rahimi","Karima Cheboub","Léon Ghosez","Gilles Hanquet"],"key":"abdeslam_akhatou_acid_2007","id":"abdeslam_akhatou_acid_2007","bibbaseid":"abdeslamakhatou-maryamrahimi-karimacheboub-longhosez-gilleshanquet-acidpromotedenantioselectiveoxygenatomtransferfromnalkylbinaphthylderivedoxaziridinesontosulfides-2007","role":"author","urls":{"Paper":"https://www.sciencedirect.com/science/article/pii/S0040402007003614"},"metadata":{"authorlinks":{}}},"bibtype":"article","biburl":"https://bibbase.org/f/RuDPTRDvZfNkJ9ecE/SynCatH-before-2019.bib","dataSources":["dXRwXwngG4P9TnZJ6","dSTKnjpdJ4acqvmgo","wyp6pqgAd7C9HyxkK","CRac9htYL7aY86pR7","hPF8a9wWuEAno5xWh","oHZsLPzALDZ8cXbER","qMo5fd827h2KcJWK4","FfZupdKq3je2BwL2c","TsP7BoYqE7M9xw6Xa"],"keywords":[],"search_terms":["acid","promoted","enantioselective","oxygen","atom","transfer","alkyl","binaphthyl","derived","oxaziridines","onto","sulfides","abdeslam akhatou","maryam rahimi","karima cheboub","léon ghosez","gilles hanquet"],"title":"Acid promoted enantioselective oxygen-atom transfer from N-alkyl binaphthyl-derived oxaziridines onto sulfides","year":2007}