D
Dean J. Tantillo
Researcher at University of California, Davis
Publications - 408
Citations - 10953
Dean J. Tantillo is an academic researcher from University of California, Davis. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 47, co-authored 368 publications receiving 9267 citations. Previous affiliations of Dean J. Tantillo include University of California & University of California, Santa Barbara.
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Journal ArticleDOI
Computational Prediction of 1H and 13C Chemical Shifts: A Useful Tool for Natural Product, Mechanistic, and Synthetic Organic Chemistry
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Small Molecule Signaling Agents: The Integrated Chemistry and Biochemistry of Nitrogen Oxides, Oxides of Carbon, Dioxygen, Hydrogen Sulfide, and Their Derived Species
Jon M. Fukuto,Samantha J. Carrington,Dean J. Tantillo,Jason G. Harrison,Louis J. Ignarro,Bruce A. Freeman,Andrew Chen,David A. Wink +7 more
TL;DR: A fundamental understanding of the chemistry of these molecules is essential to understanding their biological/physiological utility and attempts to establish the chemical basis for their signaling functions.
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Redox chemistry and chemical biology of H2S, hydropersulfides, and derived species: implications of their possible biological activity and utility.
Katsuhiko Ono,Takaaki Akaike,Tomohiro Sawa,Yoshito Kumagai,David A. Wink,Dean J. Tantillo,Adrian J. Hobbs,Péter Nagy,Ming Xian,Joseph Lin,Jon M. Fukuto +10 more
TL;DR: The basic chemical biology of H2S as well as other related or derived species is discussed and reviewed, and this review particularly focuses on the per- and polysulfides which are likely in equilibrium with free H 2S and which may be important biological effectors themselves.
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Biosynthesis via carbocations: Theoretical studies on terpene formation
TL;DR: This review describes applications of quantum chemical calculations in the field of terPene biosynthesis, with a focus on insights into the mechanisms of terpene-forming carbocation rearrangements arising from theoretical studies.
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Charge ordering in the TMTTF family of molecular conductors
TL;DR: The existence of an intermediate charge-ordered phase in the TMTTF family of charge-transfer salts is demonstrated and the absence of an associated magnetic anomaly indicates only the charge degrees of freedom are involved and the lack of evidence for a structural anomaly suggests that charge-lattice coupling is too weak to drive the transition.