@article{43971950bea74e74bcfa7fb4cfbe6331,
title = "Tandem one pot asymmetric conjugate addition-vinyl triflate formation cross coupling methodology",
abstract = "Optically active vinyl triflates are obtained and employed in a series of one pot metal-catalyzed tandem asymmetric transformations.",
keywords = "ENANTIOSELECTIVE SYNTHESIS, REAGENTS, TRANSFORMATIONS, 1,4-ADDITION, CATALYSIS, LIGANDS, ROUTE",
author = "\{M. Suarez\}, Rosa and Diego Pena and \{J. Minnaard\}, Adriaan and B.L. Feringa",
note = "Copyright (C) 2010 American Chemical Society (ACS). All Rights Reserved.; Section Code: 24-6; CODEN: OBCRAK; CAS Registry Numbers: 34946-82-2 (Copper(II) triflate); 497883-22-4 Role: CAT (Catalyst use), USES (Uses) (stereoselective prepn. of cycloalkenyl triflates via phosphoramidite-copper-catalyzed asym. conjugates addn. of organozinc reagents to cycloalkenones followed by triflation); 930-68-7 (2-Cyclohexenone); 1073-13-8 (4,4-Dimethyl-2-cyclohexenone); 1119-90-0 (Dibutylzinc); 1121-66-0 (2-Cycloheptenone) Role: RCT (Reactant), RACT (Reactant or reagent) (stereoselective prepn. of cycloalkenyl triflates via phosphoramidite-copper-catalyzed asym. conjugates addn. of organozinc reagents to cycloalkenones followed by triflation); 478015-73-5P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (stereoselective prepn. of cycloalkenyl triflates via phosphoramidite-copper-catalyzed asym. conjugates addn. of organozinc reagents to cycloalkenone",
year = "2005",
doi = "10.1039/b418028c",
language = "English",
volume = "3",
pages = "729--731",
journal = "Organic \& Biomolecular Chemistry",
issn = "1477-0520",
publisher = "ROYAL SOC CHEMISTRY",
number = "5",
}