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• W4252713780 abstract "Angewandte Chemie International EditionVolume 55, Issue 7 p. 2300-2300 Author ProfileFree Access Yixin Lu First published: 20 November 2015 https://doi.org/10.1002/anie.201508283Citations: 2AboutSectionsPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Abstract “My favorite food is lobster. My favorite place on earth is The Maldives ...” This and more about Yixin Lu can be found on page 2300. 1 Table 1. Yixin Lu Date of birth: August 21, 1970 Position: Professor, Department of Chemistry, National University of Singapore E-mail: chmlyx@nus.edu.sg Homepage: http://www.chemistry.nus.edu.sg/people/academic staff/luyx.htm Education: 1991 BSc, Fudan University, Shanghai 2000 PhD with George Just, McGill University, Montreal 2000 Postdoctoral fellow with Peter W. Schiller, Clinical Research Institute of Montreal 2000–2001 Postdoctoral fellow with Ryoji Noyori, Nagoya University Awards: 2013 GSK–SNIC Award in Organic Chemistry Research: Asymmetric catalysis and synthesis; green/sustainable chemistry; medicinal chemistry Hobbies: Sports, exercising, watching movies, sightseeing My favorite food is lobster. My favorite place on earth is The Maldives. My favorite novel is The Romance of the Three Kingdoms () by Luo Guanzhong. The downside of my job is having too many vacation days that I cannot use. If I could have dinner with three famous scientists from history, they would be Albert Einstein, Linus Pauling, and Robert B. Woodward. My best investment was real estate. My most exciting discovery to date has been amino acid based bifunctional phosphines. My worst nightmare is that someone else just published the work we are about to complete. The most exciting thing about my research is making use of natural chirality to access man-made chirality. I lose track of time when I watch decisive sports games, such as NBA finals, tennis grand slams, or the FIFA world cup. Guaranteed to make me laugh is watching episodes of Mr. Bean. I celebrate success by tasting ethanol with my family, students, or friends. My 5 top papers: References 1“Asymmetric Mannich Reaction of Fluorinated Ketoesters with a Tryptophan-Derived Bifunctional Thiourea Catalyst”: X. Han, J. Kwiatkowski, F. Xue, K.-W. Huang, Y. Lu, Angew. Chem. Int. Ed. 2009, 48, 7604; Wiley Online LibraryCASPubMedWeb of Science®Google ScholarAngew. Chem. 2009, 121, 7740. (Tertiary amine–thiourea catalysts can be derived from natural amino acids.) Wiley Online LibraryGoogle Scholar 2“Stereocontrolled Creation of All-Carbon Quaternary Stereocenters by Organocatalytic Conjugate Addition of Oxindoles to Vinyl Sulfone”: Q. Zhu, Y. Lu, Angew. Chem. Int. Ed. 2010, 49, 7753; Wiley Online LibraryCASPubMedWeb of Science®Google ScholarAngew. Chem. 2010, 122, 7919. (Multifunctional thiourea catalysts comprising amino acids for the construction of novel oxindole derivatives.) Wiley Online LibraryGoogle Scholar 3“Enantioselective [3+2] Cycloaddition of Allenes to Acrylates Catalyzed by Dipeptide-Derived Phosphines: Facile Creation of Functionalized Cyclopentenes Containing Quaternary Stereogenic Centers”: X. Han, Y. Wang, F. Zhong, Y. Lu, J. Am. Chem. Soc. 2011, 133, 1726. (Our initial report on amino acid-derived chiral phosphines in enantioselective annulation reactions.) CrossrefCASPubMedWeb of Science®Google Scholar 4“Highly Enantioselective [3+2] Annulation of Morita–Baylis–Hillman Adducts Mediated by l-Threonine-Derived Phosphines: Synthesis of 3-Spirocyclopentene-2-oxindole having Two Contiguous Quaternary Centers”: F. Zhong, X. Han, Y. Wang, Y. Lu, Angew. Chem. Int. Ed. 2011, 50, 7837; Wiley Online LibraryCASPubMedWeb of Science®Google ScholarAngew. Chem. 2011, 123, 7983. (Effective utilization of the MBH adducts as a reaction partner in phosphine-triggered asymmetric cyclization.) Wiley Online LibraryGoogle Scholar 5“Chiral Phosphine Catalyzed Asymmetric Michael Addition of Oxindoles”: F. Zhong, X. Dou, X. Han, W. Yao, Q. Zhu, Y. Meng, Y. Lu, Angew. Chem. Int. Ed. 2013, 52, 943; Wiley Online LibraryCASPubMedWeb of Science®Google ScholarAngew. Chem. 2013, 52, 943 (Enantioselective Michael addition can be mediated by amino acid-derived phosphines.) Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Citing Literature Volume55, Issue7February 12, 2016Pages 2300-2300 ReferencesRelatedInformation" @default.
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