1. Pradeep R. Varadwaj, Arpita Varadwaj, Helder M. Marques, Koichi Yamashita, “Definition of the Halogen Bond (IUPAC Recommendations 2013): A Revisit”, Crystal Growth & Design, 24:13 (2024), 5494  crossref
  2. Vasiliy G. Shtamburg, Evgeniy A. Klots, Victor V. Shtamburg, Andrey A. Anishchenko, Svitlana V. Shishkina, Alexander V. Mazepa, “Nucleophilic substitution at nitrogen atom. N-Alkoxy-N-(dimethoxyphosphoryl)ureas, synthesis and structure”, Journal of Molecular Structure, 1277 (2023), 134865  crossref
  3. Vasiliy G. Shtamburg, Victor V. Shtamburg, Andrey A. Anishchenko, Alexander V. Mazepa, Eduard B. Rusanov, “3-Alkoxy-1,5-bis(aryl)imidazolidine-2,4-diones, synthesis and structure”, Journal of Molecular Structure, 1264 (2022), 133259  crossref
  4. Stephen A. Glover, Adam A. Rosser, Amide Bond Activation, 2022, 29  crossref
  5. Stephen A. Glover, Rhiannon R. Schumacher, “Mutagenicity of N-acyloxy-N-alkoxyamides as an indicator of DNA intercalation: The role of fluorene and fluorenone substituents as DNA intercalators”, Mutation Research/Genetic Toxicology and Environmental Mutagenesis, 863-864 (2021), 503299  crossref
  6. Stephen A. Glover, Adam A. Rosser, “Heteroatom Substitution at Amide Nitrogen—Resonance Reduction and HERON Reactions of Anomeric Amides”, Molecules, 23:11 (2018), 2834  crossref
  7. Stephen A. Glover, Adam A. Rosser, “The role of substituents in the HERON reaction of anomeric amides”, Can. J. Chem., 94:12 (2016), 1169  crossref
  8. Stereoelectronic Effects, 2016, 97  crossref
  9. Stephen A. Glover, Adam A. Rosser, “HERON reactions of anomeric amides: understanding the driving force”, J of Physical Organic Chem, 28:3 (2015), 215  crossref
  10. V. G. Shtamburg, R. G. Kostyanovsky, A. V. Tsygankov, V. V. Shtamburg, O. V. Shishkin, R. I. Zubatyuk, A. V. Mazepa, S. V. Kravchenko, “Geminal systems”, Russ Chem Bull, 64:1 (2015), 62  crossref
  11. Stephen A. Glover, Adam A. Rosser, Avat (Arman) Taherpour, Ben W. Greatrex, “Formation and HERON Reactivity of Cyclic N,N-Dialkoxyamides”, Aust. J. Chem., 67:3 (2014), 507  crossref
  12. Korry L. Barnes, Anna K. Koster, Christopher S. Jeffrey, “Trapping the elusive aza-oxyallylic cation: new opportunities in heterocycloaddition chemistry”, Tetrahedron Letters, 55:34 (2014), 4690  crossref
  13. Stephen A. Glover, Adam A. Rosser, Robert M. Spence, “Studies of the Structure, Amidicity, and Reactivity of N-Chlorohydroxamic Esters and N-Chloro-β,β-dialkylhydrazides: Anomeric Amides with Low Resonance Energies”, Aust. J. Chem., 67:9 (2014), 1344  crossref
  14. V. G. Shtamburg, O. V. Shishkin, V. V. Shtamburg, R. I. Zubatyuk, A. V. Mazepa, R. G. Kostyanovsky, “N-Alkoxy-N-chloroureas in the synthesis of 3,4-dihydro-1H-2,1-benzoxazine-1-carboxamide and 1-alkoxy-1,3-dihydrobenzimidazol-2-ones”, Chem Heterocycl Comp, 49:8 (2013), 1195  crossref
  15. S. Kubik, Knowledge Updates 2013/3, 2013  crossref
  16. Christopher S. Jeffrey, Devendar Anumandla, Christopher R. Carson, “1,4-Diamination of Cyclic Dienes via a (4 + 3) Cycloaddition of Diaza-allyl Cationic Intermediates”, Org. Lett., 14:22 (2012), 5764  crossref
  17. V. G. Shtamburg, A. V. Tsygankov, O. V. Shishkin, R. I. Zubatyuk, B. V. Uspensky, V. V. Shtamburg, A. V. Mazepa, R. G. Kostyanovsky, “The properties and structure of N-chloro-N-methoxy-4-nitrobenzamide”, Mendeleev Commun., 22:3 (2012), 164–166  mathnet  crossref
  18. V. G. Shtamburg, A. V. Tsygankov, O. V. Shishkin, R. I. Zubatyuk, V. V. Shtamburg, M. V. Gerasimenko, A. V. Mazepa, R. G. Kostyanovsky, “1-Alkoxyamino-4-dimethylaminopyridinium derivatives as new representatives of O–N–N+ geminal systems and their structure†”, Mendeleev Commun., 22:2 (2012), 92–94  mathnet  crossref
  19. V. G. Shtamburg, A. V. Tsygankov, M. V. Gerasimenko, O. V. Shishkin, R. I. Zubatyuk, A. V. Mazepa, R. G. Kostyanovsky, “New approach to N,N-dialkoxy-N′-arylureas and N,N-dialkoxycarbamates”, Mendeleev Commun., 21:1 (2011), 50–52  mathnet  crossref
  20. Stephen A. Glover, Patai's Chemistry of Functional Groups, 2010  crossref
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