Zhi He, Ph.D.
Affiliations: | 2012 | Chemistry | University of Toronto, Toronto, ON, Canada |
Area:
Organic synthesisGoogle:
"Zhi He"Mean distance: 8.78 | S | N | B | C | P |
Parents
Sign in to add mentorAndrei K. Yudin | grad student | 2012 | University of Toronto | |
(Synthetic Application of Amphoteric Aziridine Aldehydes and alpha-Boryl Aldehydes.) |
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Publications
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Heckman LM, He Z, Jamison TF. (2018) Synthesis of Highly Substituted 2-Arylindoles via Copper-Catalyzed Coupling of Isocyanides and Arylboronic Acids. Organic Letters |
Adachi S, Liew SK, Lee CF, et al. (2015) Condensation-Driven Assembly of Boron-Containing Bis(Heteroaryl) Motifs Using a Linchpin Approach. Organic Letters |
Adachi S, Cognetta AB, Niphakis MJ, et al. (2015) Facile synthesis of borofragments and their evaluation in activity-based protein profiling. Chemical Communications (Cambridge, England). 51: 3608-11 |
St. Denis JD, He Z, Yudin AK. (2015) Amphoteric α-Boryl Aldehyde Linchpins in the Synthesis of Heterocycles Acs Catalysis. 5: 5373-5379 |
St Denis JD, Zajdlik A, Tan J, et al. (2014) Boron-containing enamine and enamide linchpins in the synthesis of nitrogen heterocycles. Journal of the American Chemical Society. 136: 17669-73 |
He Z, Bae M, Wu J, et al. (2014) Synthesis of highly functionalized polycyclic quinoxaline derivatives using visible-light photoredox catalysis. Angewandte Chemie (International Ed. in English). 53: 14451-5 |
Wu J, Yang X, He Z, et al. (2014) Continuous flow synthesis of ketones from carbon dioxide and organolithium or Grignard reagents. Angewandte Chemie (International Ed. in English). 53: 8416-20 |
He Z, Zajdlik A, Yudin AK. (2014) α-Borylcarbonyl compounds: from transient intermediates to robust building blocks. Dalton Transactions (Cambridge, England : 2003). 43: 11434-51 |
He Z, Jamison TF. (2014) Continuous-flow synthesis of functionalized phenols by aerobic oxidation of Grignard reagents. Angewandte Chemie (International Ed. in English). 53: 3353-7 |
He Z, Zajdlik A, Yudin AK. (2014) Air- and moisture-stable amphoteric molecules: enabling reagents in synthesis. Accounts of Chemical Research. 47: 1029-40 |