Please use this identifier to cite or link to this item: https://doi.org/10.1002/adsc.201300512
Title: Palladium-catalyzed oxidative annulation via C-H/N-H functionalization: Access to substituted pyrroles
Authors: Peng, S.
Wang, L.
Huang, J.
Sun, S.
Guo, H.
Wang, J. 
Keywords: C-H functionalization
N-H functionalization
oxidative annulations
palladium
pyrroles
Issue Date: 16-Sep-2013
Citation: Peng, S., Wang, L., Huang, J., Sun, S., Guo, H., Wang, J. (2013-09-16). Palladium-catalyzed oxidative annulation via C-H/N-H functionalization: Access to substituted pyrroles. Advanced Synthesis and Catalysis 355 (13) : 2550-2557. ScholarBank@NUS Repository. https://doi.org/10.1002/adsc.201300512
Abstract: Pyrroles, ubiquitous bioactive heterocycles in nature, are readily prepared via a palladium-catalyzed oxidative annulation of cyclic trans-enamines to various internal alkynes in the absence of a directing group. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Source Title: Advanced Synthesis and Catalysis
URI: http://scholarbank.nus.edu.sg/handle/10635/76720
ISSN: 16154150
DOI: 10.1002/adsc.201300512
Appears in Collections:Staff Publications

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