Synthesis 2017; 49(03): 604-614
DOI: 10.1055/s-0036-1588299
paper
© Georg Thieme Verlag Stuttgart · New York

Asymmetric Synthesis of 2,3,4-Trisubstituted Piperidines

Authors

  • Kadri Kriis

    Department of Chemistry, Tallinn University of Technology, Akadeemia tee 15, 12618 Tallinn, Estonia   Email: tonis.kanger@ttu.ee
  • Triin Melnik

    Department of Chemistry, Tallinn University of Technology, Akadeemia tee 15, 12618 Tallinn, Estonia   Email: tonis.kanger@ttu.ee
  • Kristiina Lips

    Department of Chemistry, Tallinn University of Technology, Akadeemia tee 15, 12618 Tallinn, Estonia   Email: tonis.kanger@ttu.ee
  • Ilona Juhanson

    Department of Chemistry, Tallinn University of Technology, Akadeemia tee 15, 12618 Tallinn, Estonia   Email: tonis.kanger@ttu.ee
  • Sandra Kaabel

    Department of Chemistry, Tallinn University of Technology, Akadeemia tee 15, 12618 Tallinn, Estonia   Email: tonis.kanger@ttu.ee
  • Ivar Järving

    Department of Chemistry, Tallinn University of Technology, Akadeemia tee 15, 12618 Tallinn, Estonia   Email: tonis.kanger@ttu.ee
  • Tõnis Kanger*

    Department of Chemistry, Tallinn University of Technology, Akadeemia tee 15, 12618 Tallinn, Estonia   Email: tonis.kanger@ttu.ee
Further Information

Publication History

Received: 28 June 2016

Accepted after revision: 01 August 2016

Publication Date:
02 September 2016 (online)


Graphical Abstract

Abstract

Two different organocatalytic approaches for the asymmetric synthesis of 2,3,4-trisubstituted piperidines were developed. Both approaches were based on an aza-Michael addition followed by cyclization and gave products in high enantiomeric excess.

Supporting Information