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Metal-free alcohol-directed regioselective heteroarylation of remote unactivated C(sp3)–H bonds

Open access
Wu, Xinxin, Zhang, Hong, Tang, Nana, Wu, Zhen, Wang, Dongping, Ji, Meishan, Xu, Yan, Wang, Min, Zhu, Chen·2018·Nature Communications

Abstract

Construction of C–C bonds via alkoxy radical-mediated remote C(sp 3)–H functionalization is largely unexplored, as it is a formidable challenge to directly generate alkoxy radicals from alcohols due to the high bond dissociation energy (BDE) of O–H bonds. Disclosed herein is a practical and elusive metal-free alcohol-directed heteroarylation of remote unactivated C(sp 3)–H bonds. Phenyliodine bis(trifluoroacetate) (PIFA) is used as the only reagent to enable the coupling of alcohols and heteroaryls. Alkoxy radicals are readily generated from free alcohols under the irradiation of visible light, which trigger the regioselective hydrogen-atom transfer (HAT). A wide range of functional groups are compatible with the mild reaction conditions. Two unactivated C–H bonds are cleaved and one new C–C bond is constructed during the reaction. This protocol provides an efficient strategy for the late-stage functionalization of alcohols and heteroaryls.

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Metadata

Authors
Wu, X., Zhang, H., Tang, N., Wu, Z., Wang, D., Ji, M., Xu, Y., Wang, M., & Zhu, C.
Venue
Nature Communications
Published
2018-08-21
Volume
9
Issue
1
Pages
3343-3343
ISSN
2041-1723 (ISSN-L)
OpenAlex
W2885117403
Cited by
206
References
1
FWCI
9.19
Type
journal article
Language
en
Open access
gold

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Wu, X., Zhang, H., Tang, N., Wu, Z., Wang, D., Ji, M., Xu, Y., Wang, M., & Zhu, C. (2018). Metal-free alcohol-directed regioselective heteroarylation of remote unactivated C(sp3)–H bonds. Nature Communications. https://doi.org/10.1038/s41467-018-05522-9

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