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Versatile pyrrole synthesis through ruthenium(II)-catalyzed alkene C-H bond functionalization on enamines.
Org Lett. 2013 Jan 04; 15(1):176-9.OL

Abstract

An efficient ruthenium(II) catalyst enabled broadly applicable oxidative alkyne annulations with electron-rich enamines to provide diversely decorated pyrroles, even in an aerobic fashion with air as the ideal oxidant.

Links

Publisher Full Text (DOI)

Authors+Show Affiliations

Wang L
Institut für Organische und Biomolekulare Chemie, Georg-August-Universität, Tammannstrasse 2, 37077 Göttingen, Germany.
Ackermann L
No affiliation info available

MeSH

AlkenesAlkynesAminesCatalysisMolecular StructureOxidation-ReductionPyrrolesRuthenium

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

23256885

Citation

Wang, Lianhui, and Lutz Ackermann. "Versatile Pyrrole Synthesis Through ruthenium(II)-catalyzed Alkene C-H Bond Functionalization On Enamines." Organic Letters, vol. 15, no. 1, 2013, pp. 176-9.
Wang L, Ackermann L. Versatile pyrrole synthesis through ruthenium(II)-catalyzed alkene C-H bond functionalization on enamines. Org Lett. 2013;15(1):176-9.
Wang, L., & Ackermann, L. (2013). Versatile pyrrole synthesis through ruthenium(II)-catalyzed alkene C-H bond functionalization on enamines. Organic Letters, 15(1), 176-9. https://doi.org/10.1021/ol303224e
Wang L, Ackermann L. Versatile Pyrrole Synthesis Through ruthenium(II)-catalyzed Alkene C-H Bond Functionalization On Enamines. Org Lett. 2013 Jan 4;15(1):176-9. PubMed PMID: 23256885.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Versatile pyrrole synthesis through ruthenium(II)-catalyzed alkene C-H bond functionalization on enamines. AU - Wang,Lianhui, AU - Ackermann,Lutz, Y1 - 2012/12/20/ PY - 2012/12/22/entrez PY - 2012/12/22/pubmed PY - 2013/5/29/medline SP - 176 EP - 9 JF - Organic letters JO - Org Lett VL - 15 IS - 1 N2 - An efficient ruthenium(II) catalyst enabled broadly applicable oxidative alkyne annulations with electron-rich enamines to provide diversely decorated pyrroles, even in an aerobic fashion with air as the ideal oxidant. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/23256885/Versatile_pyrrole_synthesis_through_ruthenium_II__catalyzed_alkene_C_H_bond_functionalization_on_enamines_ L2 - https://doi.org/10.1021/ol303224e DB - PRIME DP - Unbound Medicine ER -