• An efficient method for long‐term configurational stabilization of chiral tricyclic dipeptide via heterocomplexation approachHu, Xiaoyun; Yin, Zhongyou; Guo, Jianxin; Borovkov, Victor; Shan, ZixingChemistrySelect2019 / p. 3210-3213 https://doi.org/10.1002/slct.201900099
• Asymmetric Biginelli-like reaction catalyzed by chiral TADDOL-derived phosphoric acid bearing two hydroxyl groupsGuo, Jianxin; Zhang, Rui; Yin, Zhongyou; Hu, Xiaoyun; Borovkov, VictorThe 23rd International Electronic Conference on Synthetic Organic Chemistry15 nov 2019 - 15 dec 20192019 / 8 p. : ill https://doi.org/10.3390/ecsoc-23-06647
• Highly chemo- and regioselective synthesis and subsequent directional catalyst-free transformation of enantiopure bioxirane derivativesHu, Xiaoyun; Li, Kang; Guo, Jianxin; Wang, Cui; Ma, Ling; Borovkov, VictorTetrahedron2022 / art. 132763 https://doi.org/10.1016/j.tet.2022.132763 https://www.scopus.com/sourceid/26512 https://www.scopus.com/record/display.uri?eid=2-s2.0-85128517202&origin=inward&txGid=2c816465252d3bc54e3a0e6e0425b4ca https://jcr.clarivate.com/jcr-jp/journal-profile?journal=TETRAHEDRON&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000798186900001
• Stereoselective Biginelli-like reaction catalyzed by a chiral phosphoric acid bearing two hydroxy groupsHu, Xiaoyun; Guo, Jianxin; Wang, Cui; Zhang, Rui; Borovkov, VictorBeilstein journal of organic chemistry2020 / p. 1875−1880 https://doi.org/10.3762/bjoc.16.155 https://www.scopus.com/sourceid/4400151742 https://www.scopus.com/record/display.uri?eid=2-s2.0-85090544117&origin=inward&txGid=8438a7882862b28c556c930a96789ff6 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=BEILSTEIN%20J%20ORG%20CHEM&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000555821000001
• Stereospecific synthesis of cyclic sulfite esters with sulfur-centered chirality via diastereoselective strategy and intramolecular H-Bonding assistanceHu, Xiaoyun; Yin, Zhongyou; Guo, Jianxin; Adamson, Jasper; Fujiki, Michiya; Borovkov, VictorJournal of Organic Chemistry2021 / p. 379 - 387 https://doi.org/10.1021/acs.joc.0c02147 https://www.scopus.com/sourceid/25896 https://www.scopus.com/record/display.uri?eid=2-s2.0-85097825283&origin=resultslist&sort=plf-f&src=s&sid=4e20fc566512faafe6a1b2ec2b66583e&sot=b&sdt=b&s=DOI%2810.1021%2Facs.joc.0c02147%29&sl=25&sessionSearchId=4e20fc566512faafe6a1b2ec2b66583e&relpos=0 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=J%20ORG%20CHEM&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000606840200029