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Intermolecular, redox-neutral azidoarylation of alkenes via photoredox catalysis.
Chem Commun (Camb) 2019; 55(16):2336-2339CC

Abstract

An intermolecular, redox-neutral azidoarylation of alkenes with pyridines and TMSN3 has been reported via visible light-induced photoredox catalysis. This protocol utilized a radical addition/radical coupling sequence, allowing for facile and regioselective installation of versatile β-azido pyridines under redox-neutral and mild conditions.

Authors+Show Affiliations

State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Center for Advanced Low-Dimension Materials, College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620, China. lingling.chu1@dhu.edu.cn.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

30724310

Citation

Chen, Jian, et al. "Intermolecular, Redox-neutral Azidoarylation of Alkenes Via Photoredox Catalysis." Chemical Communications (Cambridge, England), vol. 55, no. 16, 2019, pp. 2336-2339.
Chen J, Zhu S, Qin J, et al. Intermolecular, redox-neutral azidoarylation of alkenes via photoredox catalysis. Chem Commun (Camb). 2019;55(16):2336-2339.
Chen, J., Zhu, S., Qin, J., & Chu, L. (2019). Intermolecular, redox-neutral azidoarylation of alkenes via photoredox catalysis. Chemical Communications (Cambridge, England), 55(16), pp. 2336-2339. doi:10.1039/c9cc00241c.
Chen J, et al. Intermolecular, Redox-neutral Azidoarylation of Alkenes Via Photoredox Catalysis. Chem Commun (Camb). 2019 Feb 19;55(16):2336-2339. PubMed PMID: 30724310.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Intermolecular, redox-neutral azidoarylation of alkenes via photoredox catalysis. AU - Chen,Jian, AU - Zhu,Shengqing, AU - Qin,Jian, AU - Chu,Lingling, PY - 2019/2/7/pubmed PY - 2019/2/7/medline PY - 2019/2/7/entrez SP - 2336 EP - 2339 JF - Chemical communications (Cambridge, England) JO - Chem. Commun. (Camb.) VL - 55 IS - 16 N2 - An intermolecular, redox-neutral azidoarylation of alkenes with pyridines and TMSN3 has been reported via visible light-induced photoredox catalysis. This protocol utilized a radical addition/radical coupling sequence, allowing for facile and regioselective installation of versatile β-azido pyridines under redox-neutral and mild conditions. SN - 1364-548X UR - https://www.unboundmedicine.com/medline/citation/30724310/Intermolecular_redox_neutral_azidoarylation_of_alkenes_via_photoredox_catalysis_ L2 - https://doi.org/10.1039/c9cc00241c DB - PRIME DP - Unbound Medicine ER -