guoqin xia
Affiliations: | The Scripps Research Institute, California, USA |
Area:
organometallic chemistryGoogle:
"guoqin xia"Mean distance: (not calculated yet)
Parents
Sign in to add mentorXiyan Lu | grad student | 2009-2014 | SIOC,CAS |
Stuart L. Schreiber | post-doc | 2018- | The Scripps Research Institute & Broad Institute |
Jin-Quan Yu | post-doc | 2015-2018 | The Scripps Research Institute, La Jolla, CA |
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Publications
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Hudson L, Mason JW, Westphal MV, et al. (2023) Author Correction: Diversity-oriented synthesis encoded by deoxyoligonucleotides. Nature Communications. 14: 7589 |
Hudson L, Mason JW, Westphal MV, et al. (2023) Diversity-oriented synthesis encoded by deoxyoligonucleotides. Nature Communications. 14: 4930 |
Xia G, Zhuang Z, Liu LY, et al. (2020) Ligand-Enabled β-Methylene C(sp3)-H Arylation of Masked Aliphatic Alcohols. Angewandte Chemie (International Ed. in English) |
Herron AN, Liu D, Xia G, et al. (2020) δ-C-H Mono- and Dihalogenation of Alcohols. Journal of the American Chemical Society |
Xia G, Weng J, Liu L, et al. (2019) Reversing conventional site-selectivity in C(sp)-H bond activation. Nature Chemistry |
Wang P, Verma P, Xia G, et al. (2017) Ligand-accelerated non-directed C-H functionalization of arenes. Nature. 551: 489-493 |
Jain P, Verma P, Xia G, et al. (2017) Enantioselective amine α-functionalization via palladium-catalysed C-H arylation of thioamides. Nature Chemistry. 9: 140-144 |
Shen K, Han X, Xia G, et al. (2015) Cationic Pd(ii)-catalyzed cyclization of N-tosyl-aniline tethered alkynyl ketones initiated by hydropalladation of alkynes: a facile way to 1,2-dihydro or 1,2,3,4-tetrahydroquinoline derivatives Organic Chemistry Frontiers. 2: 145-149 |
Xia G, Han X, Lu X. (2014) Efficient synthesis of heterocyle-fused β-naphthylamines via intramolecular addition to a cyano group initiated by nucleopalladation of alkynes. Organic Letters. 16: 6184-7 |
Xia G, Han X, Lu X. (2014) Pd(II)-catalyzed one-step construction of cycloalkane-fused indoles and its application in formal synthesis of (±)-aspidospermidine. Organic Letters. 16: 2058-61 |