Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Malachi W. Gillick-Healy"'
Autor:
Grazia Bencivenni, Nathalie Saraiva Rosa, Paolo Grieco, Malachi W. Gillick-Healy, Brian G. Kelly, Brendan Twamley, Mauro F. A. Adamo
Publikováno v:
Catalysts, Vol 12, Iss 7, p 803 (2022)
We report herein sharp physical evidence, i.e., single-crystal X-ray diffraction and 1H-NMR spectral data, confirming that quaternary ammonium species interact with anions via a set of directional ion–dipole cooperative +N-C-H unusual H-bonding int
Externí odkaz:
https://doaj.org/article/5b420020620c4a358ad4f28358fdf0a8
Publikováno v:
The Journal of Organic Chemistry
Herein, a high-yielding cycloaddition reaction of β-ketoesters and azides to provide 1,2,3-triazoles is described. The reactions employing 2-unsubstituted β-ketoesters were found to provide 5-methyl-1,2,3-triazoles, whereas 2-alkyl-substituted β-k
Autor:
Brian G. Kelly, Martina Costanzo, Mauro Cortigiani, Claudio Monasterolo, Malachi W. Gillick-Healy, Mauro F. A. Adamo
Publikováno v:
European Journal of Organic Chemistry. 2021:4560-4565
Autor:
Grazia Bencivenni, Andrea Ravelli, Brian G. Kelly, Malachi W. Gillick-Healy, Maria Moccia, Mauro F. A. Adamo
Publikováno v:
Organic & Biomolecular Chemistry. 18:1091-1094
Herein we report the first organocatalysed enantioselective synthesis of gingesulfonic acids and shogasulfonic acids via a mild and convenient aminothiourea-catalysed conjugate addition of bisulfite to the olefin moiety of α,β-unsaturated carbonyls
Autor:
Mauro F. A. Adamo, Francesco Alletto, Andrea Ravelli, Colm Duffy, Malachi W. Gillick-Healy, Noel McLaughlin, Stefano Lancianesi
Publikováno v:
Tetrahedron Letters. 60:1313-1316
The diastereoselective reduction of γ-keto-sulfonates to afford α,γ-substituted γ-hydroxy sulfonates has been investigated. Herein we report the first example of a diastereoselective carbonyl reduction whereby hydride attack is directed via chela
Autor:
Dario Destro, Carlo Bottinelli, Domenico Albanese, Grazia Bencivenni, Malachi W. Gillick-Healy, Brian G. Kelly, Ludovica Ferrari, Mauro F. A. Adamo
Publikováno v:
The Journal of organic chemistry. 85(8)
Herein, we present the first example of synthesis of 3,4-dihydropyran-2-ones from cinnamic thioesters via a stereoselective phase-transfer-catalyzed domino Michael-cyclization reaction with acetylacetone. The reaction proceeded under the catalysis of
Autor:
Martina Costanzo, Claudio Monasterolo, Brian G. Kelly, Mauro Cortigiani, Mauro F. A. Adamo, Malachi W. Gillick-Healy
Publikováno v:
European Journal of Organic Chemistry. 2021:4559-4559
Autor:
Malachi W. Gillick-Healy, Elizabeth V. Jennings, Kirill Nikitin, Declan G. Gilheany, Yannick Ortin, Helge Müller-Bunz
Publikováno v:
Chemistry - A European Journal. 23:2332-2339
The energy barriers in our recently discovered Walden-type inversion of chlorophosphonium salts are similar to those for Cope rearrangements of caged cyclic hydrocarbons. Therefore, we have designed a molecular system that integrates the two processe
Autor:
Helge Müller-Bunz, Yannick Ortin, Malachi W. Gillick-Healy, Kirill Nikitin, Declan G. Gilheany, Elizabeth V. Jennings
Publikováno v:
Chemistry - A European Journal. 23:2477-2477