4.6 Article

Recyclable chiral dinuclear copper(II) complexes catalyzed asymmetric Friedel-Crafts alkylation of 1-naphthol using N-tosyl aldimine

Journal

CATALYSIS COMMUNICATIONS
Volume 69, Issue -, Pages 138-142

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.catcom.2015.06.002

Keywords

Enantioselective; Friedel-Crafts reaction; 1-Naphthol; Tosyl aldimine; Copper Schiff base

Funding

  1. UGC
  2. CSIR Indus Magic Project [CSC-0123]

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A highly efficient dinuclear copper complex catalyzed Friedel-Crafts reaction has been demonstrated for the allcylation of 1-naphthol using N-tosyl aldimine. In this context, various chiral amino alcohol derived Schiff base ligands with different achiral and chiral linkers were synthesized and their copper (II) complexes were generated in situ. One of the dinuclear copper complexes with chiral linker has emerged as an efficient catalyst and affords the desired arene products in excellent enantioselectivities (ee up to 99%) with very good yields (up to 98%). The dinuclear catalyst used in this study was recoverable and recyclable with retention of its catalytic activity. (C) 2015 Elsevier B.V. All rights reserved.

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