Multiple-organocatalyst-promoted cascade reaction: a fast and efficient entry into fully substituted piperidines.

Journal article

(Figure presented) Chemical Equation presented Multiple reactions in a single pot: The development of a catalytic asymmetric approach to fully substituted piperidines, which previously remained elusive, is achieved by the use of a multicatalyst-promoted cascade reaction (see scheme). The one-pot reaction cascade is easy to perform, highly stereoselective and broad in scope, and the reaction products are high-value intermediates for multiple synthetic transformations. © 2010 Wiley-VCH Verlag GmbH and Co. KGaA.

Authors: Wang, Y; Yu, D; Liu, Y; Wei, H; Luo, Y

• Publication status: Published
• Journal: Chemistry (Weinheim an der Bergstrasse, Germany)
• Volume: 16
• Issue: 13
• Pages: 3922-3925
• Publication date: 2010-04-01
• DOI: 10.1002/chem.201000059
• EISSN: 1521-3765
• ISSN: 0947-6539
• Language: English
• Keywords: Piperidines; Stereoisomerism; Molecular Structure; Catalysis; Cyclization