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Monica Gill - Publications

Affiliations: 
Carleton University, Ottawa, Canada 
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7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Vuillermet F, Dahab MA, Abdelhamid D, Polat DE, Gill MA, Beauchemin AM. Synthesis of 1,2,4-Triazinones Exploiting the Reactivity of Diazadiene and -Isocyanate Intermediates. The Journal of Organic Chemistry. 88: 2095-2102. PMID 36749643 DOI: 10.1021/acs.joc.2c02494  0.35
2019 Gill MA, Manthorpe JM. Development of Palladium-Catalyzed Decarboxylative Allylation of Electron-Deficient Sulfones and Identification of Unusual Side Products. The Journal of Organic Chemistry. PMID 30964285 DOI: 10.1021/Acs.Joc.9B00068  0.614
2014 Manthorpe JM, Kong HI, Palko JW, Gill MA. Reduction of SulfurCarbon Bonds and of Other Heteroatoms Bonded to Tetrahedral Carbon Comprehensive Organic Synthesis: Second Edition. 8: 1031-1085. DOI: 10.1016/B978-0-08-097742-3.00830-2  0.582
2014 Kong HI, Gill MA, Hrdina AH, Crichton JE, Manthorpe JM. ChemInform Abstract: Reactivity of α-Trifluoromethanesulfonyl Esters, Amides and Ketones: Decarboxylative Allylation, Methylation, and Enol Formation. Cheminform. 45: no-no. DOI: 10.1002/chin.201417054  0.652
2013 Gill MA, Manthorpe JM. Mild, rapid, and inexpensive microwave-assisted synthesis of allylic and propargylic esters Synthetic Communications. 43: 1460-1468. DOI: 10.1080/00397911.2011.640970  0.618
2013 Kong HI, Gill MA, Hrdina AH, Crichton JE, Manthorpe JM. Reactivity of a-trifluoromethanesulfonyl esters, amides and ketones: Decarboxylative allylation, methylation, and enol formation Journal of Fluorine Chemistry. 153: 151-161. DOI: 10.1016/J.Jfluchem.2013.03.020  0.648
2013 Gill MA, Manthorpe JM. ChemInform Abstract: Mild, Rapid, and Inexpensive Microwave-Assisted Synthesis of Allylic and Propargylic Esters. Cheminform. 44: no-no. DOI: 10.1002/chin.201331037  0.637
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