3.3.2.9	1-(4-methoxyphenyl)-N-methyl-N-[(3-methyloxetan-3-yl)methyl]methanamine + H2O = 2-({[(4-methoxyphenyl)methyl](methyl)amino}methyl)-2-methylpropane-1,3-diol	(2)	-	
3.3.2.9	cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol	(1)	-	
3.3.2.9	cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol	active site structure, quantitative structure-activity relationships, molecular modelling	663432	
3.3.2.9	cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol	formation of threo-1,2-diphenyl-1,2-ethanediols from all epoxides involving anti-stereospecific opening of the oxirane ring with about 90% preference for the (S)-carbon to give nearly optically pure (R,R)-diols	661494	
3.3.2.9	cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol	reaction mechanism, catalytic triad	654503	
3.3.2.9	cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol	ring-opening reaction mechanism, overview	755352	
3.3.2.9	cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol	the catalytic triad is Asp223-Glu402-His429, the active site includes an oxyanion hole	662669	
3.3.2.9	cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol	the catalytic triad is Asp226-His431-Asp352, catalytic mechanism involving an ester intermediate formed by alkylation of an active site carboxyl group	661476	
3.3.2.9	cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol	two step mechanism with formation of of a hydroxyl-alkyl-enzyme intermediate, catalytic triad	660713	
3.3.2.9	cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol	two step mechanism with formation of of a hydroxyl-alkyl-enzyme intermediate, the catalytic triad is Asp226-His431-Glu404 with polarizing residues Tyr299 and Tyr374	660713