The principle of orbital symmetry conservation implies that the topology of the carbon backbones in transition structures for different types of pericyclic reactions will be similar. But it does not say how similar. We have shown that electrocyclic and sigmatropic rearrangements with the same electron count have transition state geometries that are strikingly similar, in fact almost indistinguishable (see above) but for the presence or absence of a simple proton (in yellow, below, in the cationic [1,8]-shift/neutral 8-pi cyclization example). These observations have also led to the concept of "transition state proton affinities", a measure of the basicity of partially formed or broken bonds in pericyclic transition structures. In addition, transition structures for sigmatropic reactions also have substructures that resemble 3-center 2-electron cations (in red, below).

 

 

We have examined various properties of transition state structures for various pericyclic reactions:

Hoffmann, R.; Tantillo, D. J. Angew. Chem. Int. Ed. 2003, 42, 5877-5882: "Breaking Down Barriers: The Liaison Between Sigmatropic Shifts, Electrocyclic Reactions and 3-Center Cations"

Ponec, R.; Bultinck, P.; Van Damme, S.; Carbo, R.; Tantillo, D. J. Theor. Chem. Acc. 2005, 113, 205-211: "Geometric and Electronic Similarities between Transition Structures for Electrocyclizations and Sigmatropic Hydrogen Shifts"

Tantillo, D. J. Annu. Rep. Prog. Chem., Sect. B 2006, 102, 269-289: "Reaction Mechanisms. Part (ii) Pericyclic Reactions"

Tantillo, D. J.; Lee, J. K. Annu. Rep. Prog. Chem., Sect. B 2007, 103, 272-293: "Reaction Mechanisms. Pericyclic Reactions"

Lee, J. K.; Tantillo, D. J. Annu. Rep. Prog. Chem., Sect. B 2008, 104, 260-283: "Reaction Mechanisms. Pericyclic Reactions"

Nouri, D. H.; Tantillo, D. J. Tetrahedron 2008, 64, 5672-5679: "Sigmatropic Shifts and Cycloadditions on Neutral, Cationic, and Anionic Pentadienyl + Butadiene Potential Energy Surfaces"

Tantillo, D. J. Angew. Chem. Int. Ed. 2009, 48, 31-32: "Using Theory and Experiment to Discover Catalysts for Electrocyclizations," invited Highlight.

Lodewyk, M. W.; Kurth, M. J.; Tantillo, D. J. J. Org. Chem. 2009, 74, 4804-4811: "Mechanisms for Formation of Diazocinones, Pyridazines, and Pyrazolines from Tetrazines - Oxyanion-Accelerated Pericyclic Cascades?"

Tantillo, D. J.; Lee, J. K. Annu. Rep. Prog. Chem., Sect. B 2009, 105, 285-309: "Reaction Mechanisms. Pericyclic Reactions"

Siebert, M. R.; Osbourn, J. M.; Brummond, K. M.; Tantillo, D. J. J. Am. Chem. Soc. 2010, 132, 11952-11966: "Differentiating Mechanistic Possibilities for the Thermal, Intramolecular [2 + 2] Cycloaddition of Allene-ynes"

Harrison, J. G.; Tantillo, D. J. Phys. Chem. Chem. Phys. 2012, 14, 14756-14759: "Fusing Cubanes to 1,5-Hexadiene," invited for themed issue on "Predicting New Molecules by Quantum Chemical Methods".

Maity, P.; Pemberton, R. P.; Tantillo, D. J.; Tambar, U. K. J. Am. Chem. Soc. 2013, 135, 16380-16383: "Bronsted Acid Catalyzed Enantioselective Indole Aza-Claisen Rearrangement Mediated by an Arene CH-O Interaction"

Painter, P. P.; Wong, B. M.; Tantillo, D. J. Org. Lett. 2014, 16, 4818-4821: "Facilitating the Cope Rearrangement by Partial Protonation - Implications for Synthesis and Biosynthesis"

Rasik, C. M.; Hong, Y. J.; Tantillo, D. J.; Brown, M. K. Org. Lett. 2014, 16, 5168-5171: "Origins of Diastereoselectivity in Lewis Acid-Promoted Ketene-Alkene [2+2] Cycloadditions"

Slauson, S. R.; Pemberton, R. P.; Ghosh, P.; Tantillo, D. J.; Aube, J. J. Org. Chem. 2015, 80, 260-5271: "Domino Acylation/Diels-Alder Synthesis of N-Alkyl-octahydroisoquinolin-1-one-8-carboxylic Acids Under Low-Solvent Conditions"

 

 

 

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