Palladium-catalyzed oxidative annulation via C-H/N-H functionalization: Access to substituted pyrroles

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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