@ARTICLE{Lopez20071411,
author={López, C.S. and Faza, O.N. and Souto, J.A. and Álvarez, R. and De Lera, Á.R.},
title={Pseudopericyclic design drives antara-antara [1,5] methylene sigmatropic shifts from a stepwise to a concerted mechanism},
journal={Journal of Computational Chemistry},
year={2007},
volume={28},
number={8},
pages={1411-1416},
doi={10.1002/jcc.20620},
abstract={Antara-antara [1,5]-methylene sigmatropic shifts of propenylidene cyclopropane and its heteroanalogues are shown to proceed through concerted or stepwise mechanisms depending on a delicate balance that is directly related to the presence or absence of heteroatoms at the termini atoms of the rearrangement. Lowering of activation energies upon heteroatom replacement are more significant for the oxacyclopropane analogues 1D, 1E, and 1F but double heterosubstitution is still needed to achieve a pseudopericyclic reaction. In fact only after reaching a pseudopericyclic process the energy balance favors the concerted pathway. Negligible NICS values and a clear disconnection in the ACID plot as well as some structural and energetical parameters reveal the pseudopericyclic nature of this concerted antara-antara [1,5]CH2 sigmatropic shift. Although the product of the pseudopericyclic process is unprecedented, similar cycloisomerizations after allene activation should be considered within this hitherto undescribed reactions. © 2007 Wiley Periodicals, Inc.},
}

{"_id":"sgZa23DiXvLimMf7s","bibbaseid":"lpez-faza-souto-lvarez-delera-pseudopericyclicdesigndrivesantaraantara15methylenesigmatropicshiftsfromastepwisetoaconcertedmechanism-2007","author_short":["López, C.","Faza, O.","Souto, J.","Álvarez, R.","De Lera, Á."],"bibdata":{"bibtype":"article","type":"article","author":[{"propositions":[],"lastnames":["López"],"firstnames":["C.S."],"suffixes":[]},{"propositions":[],"lastnames":["Faza"],"firstnames":["O.N."],"suffixes":[]},{"propositions":[],"lastnames":["Souto"],"firstnames":["J.A."],"suffixes":[]},{"propositions":[],"lastnames":["Álvarez"],"firstnames":["R."],"suffixes":[]},{"propositions":[],"lastnames":["De","Lera"],"firstnames":["Á.R."],"suffixes":[]}],"title":"Pseudopericyclic design drives antara-antara [1,5] methylene sigmatropic shifts from a stepwise to a concerted mechanism","journal":"Journal of Computational Chemistry","year":"2007","volume":"28","number":"8","pages":"1411-1416","doi":"10.1002/jcc.20620","abstract":"Antara-antara [1,5]-methylene sigmatropic shifts of propenylidene cyclopropane and its heteroanalogues are shown to proceed through concerted or stepwise mechanisms depending on a delicate balance that is directly related to the presence or absence of heteroatoms at the termini atoms of the rearrangement. Lowering of activation energies upon heteroatom replacement are more significant for the oxacyclopropane analogues 1D, 1E, and 1F but double heterosubstitution is still needed to achieve a pseudopericyclic reaction. In fact only after reaching a pseudopericyclic process the energy balance favors the concerted pathway. Negligible NICS values and a clear disconnection in the ACID plot as well as some structural and energetical parameters reveal the pseudopericyclic nature of this concerted antara-antara [1,5]CH2 sigmatropic shift. Although the product of the pseudopericyclic process is unprecedented, similar cycloisomerizations after allene activation should be considered within this hitherto undescribed reactions. © 2007 Wiley Periodicals, Inc.","bibtex":"@ARTICLE{Lopez20071411,\nauthor={López, C.S. and Faza, O.N. and Souto, J.A. and Álvarez, R. and De Lera, Á.R.},\ntitle={Pseudopericyclic design drives antara-antara [1,5] methylene sigmatropic shifts from a stepwise to a concerted mechanism},\njournal={Journal of Computational Chemistry},\nyear={2007},\nvolume={28},\nnumber={8},\npages={1411-1416},\ndoi={10.1002/jcc.20620},\nabstract={Antara-antara [1,5]-methylene sigmatropic shifts of propenylidene cyclopropane and its heteroanalogues are shown to proceed through concerted or stepwise mechanisms depending on a delicate balance that is directly related to the presence or absence of heteroatoms at the termini atoms of the rearrangement. Lowering of activation energies upon heteroatom replacement are more significant for the oxacyclopropane analogues 1D, 1E, and 1F but double heterosubstitution is still needed to achieve a pseudopericyclic reaction. In fact only after reaching a pseudopericyclic process the energy balance favors the concerted pathway. Negligible NICS values and a clear disconnection in the ACID plot as well as some structural and energetical parameters reveal the pseudopericyclic nature of this concerted antara-antara [1,5]CH2 sigmatropic shift. Although the product of the pseudopericyclic process is unprecedented, similar cycloisomerizations after allene activation should be considered within this hitherto undescribed reactions. © 2007 Wiley Periodicals, Inc.},\n}\n\n","author_short":["López, C.","Faza, O.","Souto, J.","Álvarez, R.","De Lera, Á."],"key":"Lopez20071411","id":"Lopez20071411","bibbaseid":"lpez-faza-souto-lvarez-delera-pseudopericyclicdesigndrivesantaraantara15methylenesigmatropicshiftsfromastepwisetoaconcertedmechanism-2007","role":"author","urls":{},"metadata":{"authorlinks":{}},"downloads":0,"html":""},"bibtype":"article","biburl":"http://csilval.webs.uvigo.es/scopus.bib","dataSources":["ScMRjgBATXPCMSMM8"],"keywords":[],"search_terms":["pseudopericyclic","design","drives","antara","antara","methylene","sigmatropic","shifts","stepwise","concerted","mechanism","lópez","faza","souto","álvarez","de lera"],"title":"Pseudopericyclic design drives antara-antara [1,5] methylene sigmatropic shifts from a stepwise to a concerted mechanism","year":2007}