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Organocatalytic atroposelective construction of axially chiral N, N- and N, S-1,2-azoles through novel ring formation approach.

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Title: Organocatalytic atroposelective construction of axially chiral N, N- and N, S-1,2-azoles through novel ring formation approach.
Authors: Chang Y; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China., Xie C; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China., Liu H; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China., Huang S; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China., Wang P; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China., Qin W; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China. wenling.qin@cqu.edu.cn., Yan H; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China. yhl198151@cqu.edu.cn.
Source: Nature communications [Nat Commun] 2022 Apr 11; Vol. 13 (1), pp. 1933. Date of Electronic Publication: 2022 Apr 11.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Organocatalytic atroposelective construction of axially chiral N, N- and N, S-1,2-azoles through novel ring formation approach.
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  Data: <searchLink fieldCode="AU" term="%22Chang+Y%22">Chang Y</searchLink>; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China.<br /><searchLink fieldCode="AU" term="%22Xie+C%22">Xie C</searchLink>; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China.<br /><searchLink fieldCode="AU" term="%22Liu+H%22">Liu H</searchLink>; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China.<br /><searchLink fieldCode="AU" term="%22Huang+S%22">Huang S</searchLink>; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China.<br /><searchLink fieldCode="AU" term="%22Wang+P%22">Wang P</searchLink>; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China.<br /><searchLink fieldCode="AU" term="%22Qin+W%22">Qin W</searchLink>; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China. wenling.qin@cqu.edu.cn.<br /><searchLink fieldCode="AU" term="%22Yan+H%22">Yan H</searchLink>; Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, 401331, Chongqing, P. R. China. yhl198151@cqu.edu.cn.
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  Data: <searchLink fieldCode="JN" term="%22101528555%22">Nature communications</searchLink> [Nat Commun] 2022 Apr 11; Vol. 13 (1), pp. 1933. <i>Date of Electronic Publication: </i>2022 Apr 11.
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