Chris Kalnmals
Affiliations: | 2013-2019 | Chemistry | Stanford University, Palo Alto, CA |
Area:
Organic synthesis, asymmetric catalysisWebsite:
https://www.linkedin.com/in/chriskalnmals/Google:
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Publications
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Trost BM, Kalnmals CA, Ramakrishnan D, et al. (2020) Ruthenium-Catalyzed Asymmetric Allylic Alkylation of Isatins. Organic Letters |
Trost BM, Kalnmals CA. (2019) Annulative Allylic Alkylation Reactions Between Dual Electrophiles and Dual Nucleophiles: Applications in Complex Molecule Synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Trost BM, Spohr SM, Rolka AB, et al. (2019) Desymmetrization of Phosphinic Acids via Pd-Catalyzed Asymmetric Allylic Alkylation: Rapid Access to -Chiral Phosphinates. Journal of the American Chemical Society |
Trost BM, Kalnmals CA. (2019) Sulfones as Chemical Chameleons: Versatile Synthetic Equivalents of Small Molecule Synthons. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Trost BM, Gnanamani E, Hung CJ, et al. (2019) Synthesis of Chiral, Densely Substituted Pyrrolidones via Phosphine-Catalyzed Cycloisomerization. Organic Letters |
Trost BM, Gnanamani E, Kalnmals CA, et al. (2019) Direct Enantio- and Diastereoselective Vinylogous Addition of Butenolides to Chromones Catalyzed by Zn-ProPhenol. Journal of the American Chemical Society |
Trost BM, Kalnmals CA, Tracy JS, et al. (2018) Highly Chemoselective Deprotection of the 2,2,2-Trichloroethoxycarbonyl (Troc) Protecting Group. Organic Letters |
Trost BM, Kalnmals C. (2018) Sulfones as Synthetic Linchpins: Transition Metal-Free sp3-sp2 and sp2-sp2 Cross-Couplings Between Geminal bis(Sulfones) and Organolithium Compounds. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Trost BM, Gnanamani E, Tracy JS, et al. (2017) Zn-ProPhenol Catalyzed Enantio- and Diastereoselective Direct Vinylogous Mannich Reactions between α,β- and β,γ-Butenolides and Aldimines. Journal of the American Chemical Society |
Trost BM, Kalnmals CA. (2017) Stereoselective Synthesis of Exocyclic Tetrasubstituted Vinyl Halides via Ru-Catalyzed Halotropic Cycloisomerization of 1,6-Haloenynes. Organic Letters |