Michael Harmata, Ph.D.
Affiliations: | 1986- | Chemistry | The University of Missouri |
Area:
Organic SynthesisWebsite:
http://chemistry.missouri.edu/people/harmata.htmlGoogle:
"Michael Harmata"Mean distance: 7.4 | S | N | B | C | P |
Parents
Sign in to add mentorScott E. Denmark | grad student | 1980-1985 | UIUC |
Paul A. Wender | post-doc | 1985-1986 | Stanford |
Children
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Publications
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Tu J, Clark MM, Harmata M. (2022) First synthesis of an ABCE ring substructure of daphnicyclidin A. Organic & Biomolecular Chemistry. 20: 6547-6549 |
Tu J, Ripa RA, Kelley SP, et al. (2022) Intramolecular (4+3) Cycloadditions of Oxidopyridinium Ions: Towards Daphnicyclidin A. Chemistry (Weinheim An Der Bergstrasse, Germany). e202200370 |
Fu C, Kelley SP, Tu J, et al. (2021) Generation of the 7-Azabicyclo[4.3.1]decane Ring System via (4 + 3) Cycloaddition of Oxidopyridinium Ions. The Journal of Organic Chemistry |
Wärnmark K, Dawaigher S, Lindbäck E, et al. (2020) Mono-endo-6-N,N-diethylcarbamoyl and bis-endo,endo-6,12-N,N-diethylcarbamoyl derivatives of Tröger’s base. Synthesis and exo-endo isomerization study Arkivoc. 2020: 67-81 |
Harmata M, J. Cramer C, Garimalla A, et al. (2019) The Effect of Lithium Ion on the Stereoselectivity of the Intramolecular Michael Addition of an N-Arylsulfoximine Anion Heterocycles. 99: 1117 |
Tata RR, Fu C, Kelley SP, et al. (2018) Synthesis of 3-(Arylsulfonyl)-3-pyrrolines from Allenyl Sulfonamides by Silver Ion Catalysis. Organic Letters |
Harmata M. (2018) Fun with (4+3)-Cycloadditions Synlett. 30: 532-541 |
Harmata M, Garimalla A. (2018) Derivatives of Alkyl 2-Hydroxy-3-oxocyclopent-1-enecarboxylates and Intermolecular [4+2] Cycloadditions of Cyclopentadienones Prepared Therefrom Synthesis. 50: 4483-4489 |
Harmata M, Topinka M. (2018) Synthesis of (Z)-2-[(tert-Butyldimethylsilyl)oxy]-3-(phenylthio) acrylaldehyde Synthesis. 50: 4476-4482 |
Tata RR, Harmata M. (2018) Sulfinate Allenyl Carbenoids: Synthesis of 2,5-Dihydrofurans by Domino Rearrangement and Cyclization European Journal of Organic Chemistry. 2018: 372-375 |