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Molecular Modeling of Anti-Bredt Compounds

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Department of Chemistry, National University of Singapore, Singapore 117543, Singapore
Cite this: J. Chem. Inf. Model. 2005, 45, 2, 334–338
Publication Date (Web):February 2, 2005
https://doi.org/10.1021/ci0497354
Copyright © 2005 American Chemical Society
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Abstract

The molecular structure and thermochemical stability of 40 bicyclic alkenes and imines containing between five and eight heavy atoms has been investigated computationally by high-level G3/B3LYP method. The same method was also used to study their building blocks:  monocyclic alkenes and imines. The relative stability of isomers, standard enthalpies of formation and strain energies are discussed and compared. Our results suggest that molecular mechanics provides an unsatisfactory description of strain energies in bridgehead alkenes. Some bridgehead alkene and imine species represent structures which are not local minima on the potential energy surface and are hence unlikely to be isolated. Furthermore, some bicyclic alkenes and imines have open-shell 1,2-diradical character.

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 Corresponding author e-mail:  [email protected]

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List of isodesmic reactions, calculated total energies, optimized geometries and zero point energies. This material is available free of charge via the Internet at http://pubs.acs.org.

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Cited By


This article is cited by 8 publications.

  1. Stephanie R. Hare, Marina Orman, Faizunnahar Dewan, Elizabeth Dalchand, Camilla Buzard, Sadia Ahmed, Julia C. Tolentino, Ulweena Sethi, Kelly Terlizzi, Camille Houferak, Aliza M. Stein, Alexandra Stedronsky, Dasan M. Thamattoor, Dean J. Tantillo, and Dina C. Merrer . Experimental and Computational Mechanistic Investigation of Chlorocarbene Additions to Bridgehead Carbene–Anti-Bredt Systems: Noradamantylcarbene–Adamantene and Adamantylcarbene–Homoadamantene. The Journal of Organic Chemistry 2015, 80 (10) , 5049-5065. https://doi.org/10.1021/acs.joc.5b00456
  2. Michal Szostak and Jeffrey Aubé . Chemistry of Bridged Lactams and Related Heterocycles. Chemical Reviews 2013, 113 (8) , 5701-5765. https://doi.org/10.1021/cr4000144
  3. Zhihua Lin, Junling Sun, Bisera Efremovska, Ralf Warmuth. Assembly of Water-Soluble, Dynamic, Covalent Container Molecules and Their Application in the Room-Temperature Stabilization of Protoadamantene. Chemistry - A European Journal 2012, 18 (40) , 12864-12872. https://doi.org/10.1002/chem.201200602
  4. . Bredt's Rule. 2010,,https://doi.org/10.1002/9780470638859.conrr116
  5. Achim Stolle, Bernd Ondruschka, Henning Hopf. Thermal Rearrangements of Monoterpenes and Monoterpenoids. Helvetica Chimica Acta 2009, 92 (9) , 1673-1719. https://doi.org/10.1002/hlca.200900041
  6. D. Barker. Pyridines and their Benzo Derivatives: Reactivity of Reduced Compounds. 2008,,, 171-216. https://doi.org/10.1016/B978-008044992-0.00604-0
  7. Sergei I. Kozhushkov, Thomas Preuß, Dmitrii S. Yufit, Judith A. K. Howard, Kathrin Meindl, Stephan Rühl, Chiyo Yamamoto, Yoshio Okamoto, Peter R. Schreiner, B. Christopher Rinderspacher, Armin de Meijere. 4,7,11-Triheterotrishomocubanes – Propeller-Shaped Highly Symmetrical Chiral Molecules Derived from Barrelene. European Journal of Organic Chemistry 2006, 2006 (11) , 2590-2600. https://doi.org/10.1002/ejoc.200600019
  8. Igor Novak. Molecular Modeling of anti-Bredt Compounds.. ChemInform 2005, 36 (22) https://doi.org/10.1002/chin.200522222

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