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Title:	A re-investigation of Modena’s protocol for the asymmetric oxidation of prochiral sulfides
Source:	Tetrahedron: asymmetry [0957-4166] Massa, Antonio yr:2005

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description	7.	Volcho, K. P. "Metal complexes in asymmetric oxidation of sulfides." Russian journal of organic chemistry 39.11 (2003): 1537-1552.
description	8.	Schaumann, E. "A new general route to acceptor-substituted vinyloxiranes via siloxyoxiranes - novel promising synthetic building blocks." Synthesis 2002.2 (2002): 191-194.
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description	11.	Doyle, G. "Synthesis of. beta.-diketonate chelates of the bis (cyclopentadienyl) titanium (IV) moiety: infrared and proton magnetic resonance spectra." Inorganic chemistry 6.6 (1967): 1111-1115.
description	12.	Merz, K. "AM1 Parameters for the Prediction of H-1 and C-13 NMR Chemical Shifts in Proteins." The journal of physical chemistry. A 113.43 (2009): 11550-11559.
description	13.	Forcato, M. "A 'waterproof' catalyst for the oxidation of secondary amines to nitrones with alkyl hydroperoxides." Tetrahedron letters 44.1 (2003): 49-52.
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description	15.	Kwiatkowski, E. "Chiral dioxovanadium(V) complexes with single condensation products of 1,2-diaminocyclohexane and aromatic o-hydroxycarbonyl compounds: Synthesis, characterization, catalytic properties and structure." Polyhedron 26.12 (2007): 2559-2568.
description	16.	Ishii, Y. "Innovation of hydrocarbon oxidation with molecular oxygen and related reactions." Advanced synthesis & catalysis 343.5 (2001): 393-427.
description	17.	Legros, J. "Investigations on the iron-catalyzed asymmetric sulfide oxidation." Chemistry : a European journal 11.4 (2005): 1086-1092.
description	18.	Wardrop, Duncan J. "Template-Directed C-H Insertion: Synthesis of the Dioxabicyclo[3.2.1]octane Core of the Zaragozic Acids." Organic letters 3.15 (2001): 2261-.
description	19.	Reetz, Manfred T. "Stereoselective synthesis of Î²-amino alcohols from optically active Î±-amino acids." Angewandte chemie 99.11 (1987): 1186-1188.
description	20.	Couche, E. "Asymmetric synthesis of the cis- and trans-3,4-dihydro-2,4,8-trihydroxynaphthalen-1(2H)-ones." Helvetica chimica acta 86.1 (2003): 210-221.