A chemo- and regioselective C6-functionalization of 2,3-disubstituted indoles: highly efficient synthesis of diarylindol-6-ylmethanes
Wu, Qiong, Li, Gui-Lin, Yang, Shuang, Shi, Xiao-Qin, Huang, Tian-Zi, Du, Xi-Hua, Chen, Yan
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Published in Organic & biomolecular chemistry (27.03.2019)
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Chiral Brønsted acid-catalyzed alkylation of C3-substituted indoles with o-hydroxybenzyl alcohols: highly enantioselective synthesis of diarylindol-2-ylmethanes and evaluation on their cytotoxicity
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Published in Tetrahedron: asymmetry (01.05.2016)
Published in Tetrahedron: asymmetry (01.05.2016)
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A chemo- and regioselective C6-functionalization of 2,3-disubstituted indoles: highly efficient synthesis of diarylindol-6-ylmethanesElectronic supplementary information (ESI) available: Original NMR spectra of products 3. CCDC 1893731 for 3ae. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c9ob00283a
Wu, Qiong, Li, Gui-Lin, Yang, Shuang, Shi, Xiao-Qin, Huang, Tian-Zi, Du, Xi-Hua, Chen, Yan
Year of Publication 27.03.2019
Year of Publication 27.03.2019
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ChemInform Abstract: Chiral Broensted Acid‐Catalyzed Alkylation of C3‐Substituted Indoles with o‐Hydroxybenzyl Alcohols: Highly Enantioselective Synthesis of Diarylindol‐2‐ylmethanes and Evaluation on Their Cytotoxicity
Wu, Qiong, Ma, Chun, Du, Xi‐hua, Chen, Yan, Huang, Tian‐zi, Shi, Xiao‐qin, Tu, Shu‐jiang, Cai, Pei‐jun
Published in ChemInform (01.07.2016)
Published in ChemInform (01.07.2016)
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Published in Neural regeneration research (01.06.2017)
Published in Neural regeneration research (01.06.2017)
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