Enantioselective Michael Addition of Diethyl Malonate on Substituted Chalcone Catalysed by Nickel-Sparteine Complex

Journal Title: Organic Chemistry: Current Research - Year 2017, Vol 6, Issue 1

Abstract

A series of transition metal with Sparteine a novel chiral catalyst was facilely synthesized, all of which contain a chiral Sparteine unit as a bidentate ligand. These bidentate chiral auxiliaries were found to be an efficient chiral catalyst in nickel-mediated, enantioselective Michael addition of Diethyl malonate to substituted chalcone. The corresponding adducts were obtained in good yields (80-91%) under simple and clean reaction condition.

Authors and Affiliations

Manojkumar U Chopade

Keywords

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  • EP ID EP358237
  • DOI 10.4172/2161-0401.1000178
  • Views 127
  • Downloads 0

How To Cite

Manojkumar U Chopade (2017). Enantioselective Michael Addition of Diethyl Malonate on Substituted Chalcone Catalysed by Nickel-Sparteine Complex. Organic Chemistry: Current Research, 6(1), 1-3. https://europub.co.uk/articles/-A-358237