23 results on '"Cloonan, Martin O."'
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2. Synthesis and characterisation of thermo-sensitive terpolymer hydrogels for drug delivery applications
3. Application of the Cplex-isoelectronic theory to electrocyclisations, sigmatropic rearrangements, cheletropic reactions and antiaromaticity: Consistent with Santilli's hadronic chemistry
4. A new electronic theory of pericyclic chemistry and aromaticity is proposed: The Cplex-isoelectronic theory. Consistent with Santilli's hadronic chemistry
5. A chemist's view of J.M. Calo's comments on: “A new gaseous and combustible form of water” by R.M. Santilli (Int. J. Hydrogen Energy 2006:31(9), 1113–1128)
6. ChemInform Abstract: Origin of the Torquoselectivity Observed in the Thermal Ring-Opening of Cyclobutenes Based on the Cplex-isoelectronic Theory and Expanded Robinson Electronic Theory
7. ChemInform Abstract: Thiadiazolium Ylides: Substituted 2H-1,3,5-Thiadiazines and 1,4,5-Trisubstituted-imidazoles from 1,2,4- and 1,2,5-Thiadiazolium-2-unsubstituted Methanide (Ylide) Systems: Ring Expansions and Ring Interconversions via Sulfur-Nitrogen H
8. ChemInform Abstract: Synthesis of Heterocycles by Radical Cyclization.
9. ChemInform Abstract: Cascade Radical Synthesis of Heteroarenes via Iminyl Radicals.
10. Synthesis of heteroarenes using cascade radical cyclisation via iminyl radicals
11. The reaction of unstabilised 1,3,4-oxadiazolium-N-methanide 1,3-dipoles with alkenes: N-substituted Δ-2-pyrrolines: contrast with the 1,3,4-thiadiazolium analogue
12. ChemInform Abstract: A New Tricyclic Ring and a Nitrogen—Sulfur Analogue of the Tri‐pentagon Bowl. Substituted 5,6,7,7a‐Tetrahydropyrrolo [2,1‐b]‐1,3,4‐thiadiazole‐endo‐6,7‐dicarboxyimides.
13. Synthesis of heterocycles by radical cyclisation
14. ChemInform Abstract: Synthesis of Heteroarenes via Radical Cyclization onto Nitriles.
15. Synthesis of Heteroarenes via Radical Cyclisation onto Nitriles
16. ChemInform Abstract: 1,2,3‐Thiadiazol‐3‐ium‐3‐methanide (ylide) 1,3‐Dipoles: Cycloaddition—Rearrangement Sequences Leading to Substituted 1‐(2‐Vinylthioethenyl)pyrazole Systems: Azolium 1,3‐Dipoles.
17. 1,2,3-Thiadiazol-3-ium-3-methanide (ylide) 1,3-dipoles: cycloaddition–rearrangement sequences leading to substituted 1-(2-vinylthioethenyl)pyrazole systems: azolium 1,3-dipoles
18. Thiadiazolium ylides: Substituted 2H-1,3,5-thiadiazines and 1,4,5-trisubstituted-imidazoles from 1,2,4- and 1,2,5-thiadiazolium-2-unsubstituted methanide (ylide) systems: ring expansions and ring interconversions via sulfur-nitrogen heterotriene intermediates. Mechanistic ab initio calculations. Azolium 1,3-dipoles
19. New 1,3,4-thiadiazolium-3-(unsubstituted) methanide 1,3-dipoles (azolium 1,3-dipoles): useful synthons at −60 °C: a new ring interconversion route to 1,2,3-trisubstituted and 1,2,3,4-tetrasubstituted 1-{[1-(vinylthio)-1-phenylmethylidene]amino}pyrroles
20. A new tricyclic ring and a nitrogensulfur analogue of the tri-pentagon bowl. Substituted 5,6,7,7a-tetrahydropyrrolo[2,1-b]-1,3,4-thiadiazole-endo-6,7-dicarboxyimides
21. ChemInform Abstract: Cascade Radical Synthesis of Heteroarenes via Iminyl Radicals.
22. ChemInform Abstract: Synthesis of Heterocycles by Radical Cyclization.
23. ChemInform Abstract: Thiadiazolium Ylides: Substituted 2H-1,3,5-Thiadiazines and 1,4,5-Trisubstituted-imidazoles from 1,2,4- and 1,2,5-Thiadiazolium-2-unsubstituted Methanide (Ylide) Systems: Ring Expansions and Ring Interconversions via Sulfur-Nitrogen Heterotriene Intermediates. Mechanistic ab initio Calculations. Azolium 1,3-Dipoles.
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