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pro vyhledávání: '"Charles L. Perrin"'
Autor:
Charles L. Perrin
Publikováno v:
Molecules, Vol 28, Iss 11, p 4462 (2023)
Short, strong, symmetric, low-barrier hydrogen bonds (H-bonds) are thought to be of special significance. We have been searching for symmetric H-bonds by using the NMR technique of isotopic perturbation. Various dicarboxylate monoanions, aldehyde eno
Externí odkaz:
https://doaj.org/article/d1ed3b874ae544f8893acd6cfc55a0a3
Autor:
Annadka Shrinidhi, Charles L. Perrin
Publikováno v:
ACS omega, vol 7, iss 26
Alkylation of aromatics and formation of a new C-C bond is usually achieved by the electrophilic attack of an activated carbon species on an electron-rich aromatic ring. Herein, we report an alternative method for alkylation of aromatics via nucleoph
Autor:
Charles L. Perrin
Publikováno v:
The Journal of organic chemistry, vol 87, iss 11
After many years of unsuccessful attempts, monomeric malonic anhydrides were prepared by ozonolysis of ketene dimers, a procedure validated by model studies. The structure proof relied most heavily on IR absorption at 1820 cm-1 and a Raman band at 19
Autor:
Charles L Perrin, Jiwoo Kim
Publikováno v:
Physical Chemistry Chemical Physics. 24:18978-18982
The base-catalyzed aldol condensation between benzaldehyde and p-acetylbenzoic acid in water shows an inverse solvent kinetic isotope effect, k3,D2O/k3,H2O, of 1.33 ± 0.03.
Autor:
Charles L. Perrin
Publikováno v:
The Journal of Organic Chemistry. 86:14245-14249
On a substituted benzene ring the position that bears the substituent is designated as the ipso position. This Perspective presents the history behind that designation.
Autor:
Annadka Shrinidhi, Charles L. Perrin
Publikováno v:
Organic letters, vol 23, iss 17
Enediynes are widely studied to understand their cycloaromatization and the trapping of the resulting p-dehydrobenzene diradical. However, few model substrates are known, and they are hard to synthesize and difficult to handle. Herein we report cyclo
Autor:
Charles L. Perrin, Israel Agranat, Alessandro Bagno, Silvia E. Braslavsky, Pedro Alexandrino Fernandes, Jean-François Gal, Guy C. Lloyd-Jones, Herbert Mayr, Joseph R. Murdoch, Norma Sbarbati Nudelman, Leo Radom, Zvi Rappoport, Marie-Françoise Ruasse, Hans-Ullrich Siehl, Yoshito Takeuchi, Thomas T. Tidwell, Einar Uggerud, Ian H. Williams
Publikováno v:
Pure and Applied Chemistry, vol 94, iss 4
Perrin, C L, Agranat, I, Bagno, A, Braslavsky, S E, Fernandes, P A, Gal, J, Lloyd-jones, G C, Mayr, H, Murdoch, J R, Nudelman, N S, Radom, L, Rappoport, Z, Ruasse, M, Siehl, H, Takeuchi, Y, Tidwell, T T, Uggerud, E & Williams, I H 2022, ' Glossary of terms used in physical organic chemistry (IUPAC Recommendations 2021) ', Pure and applied chemistry, vol. 94, no. 4, pp. 353-534 . https://doi.org/10.1515/pac-2018-1010
Perrin, C L, Agranat, I, Bagno, A, Braslavsky, S E, Fernandes, P A, Gal, J, Lloyd-jones, G C, Mayr, H, Murdoch, J R, Nudelman, N S, Radom, L, Rappoport, Z, Ruasse, M, Siehl, H, Takeuchi, Y, Tidwell, T T, Uggerud, E & Williams, I H 2022, ' Glossary of terms used in physical organic chemistry (IUPAC Recommendations 2021) ', Pure and applied chemistry, vol. 94, no. 4, pp. 353-534 . https://doi.org/10.1515/pac-2018-1010
This Glossary contains definitions, explanatory notes, and sources for terms used in physical organic chemistry. Its aim is to provide guidance on the terminology of physical organic chemistry, with a view to achieving a consensus on the meaning and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca66ccc111e35a67246f5b9ec5ba0e8e
https://escholarship.org/uc/item/2rx9m9pg
https://escholarship.org/uc/item/2rx9m9pg
Autor:
Charles L. Perrin
Publikováno v:
Journal of Physical Organic Chemistry, vol 35, iss 11
Autor:
Charles L Perrin
Publikováno v:
Physical chemistry chemical physics : PCCP. 23(38)
The referenced article in PCCP presents calculations of solvent kinetic isotope effects that indicate that the rate-limiting step in base-catalyzed chalcone formation in aqueous solution becomes the second enolization. This disputes our previous conc
Autor:
Yifan Wu, Charles L. Perrin
Publikováno v:
Journal of the American Chemical Society, vol 141, iss 9
The enols of 4-cyano-2,2,6,6-tetramethyl-3,5-heptanedione and of nitromalonamide were prepared as statistical mixtures of 18O n ( n = 0, 1, 2) isotopologues. The symmetries of their hydrogen bonds were probed by isotopic perturbation of their 13CO NM