Year |
Citation |
Score |
2020 |
Handy ST, Kafle A, Bhattarai S. An Unusual Triazole Synthesis from Aurones Synthesis. 52: 2337-2346. DOI: 10.1055/s-0040-1708019 |
0.367 |
|
2017 |
Kafle A, Handy ST. A one-pot, copper-catalyzed azidation/click reaction of aryl and heteroaryl bromides in an environmentally friendly deep eutectic solvent Tetrahedron. 73: 7024-7029. DOI: 10.1016/J.TET.2017.10.050 |
0.341 |
|
2014 |
Handy S, Westbrook NM. A mild synthesis of bis(indolyl)methanes using a deep eutectic solvent Tetrahedron Letters. 55: 4969-4971. DOI: 10.1016/j.tetlet.2014.07.024 |
0.378 |
|
2014 |
Handy S, Wright M. An acid-free Pictet-Spengler reaction using deep eutectic solvents (DES) Tetrahedron Letters. 55: 3440-3442. DOI: 10.1016/J.Tetlet.2014.04.077 |
0.354 |
|
2013 |
Handy S, Lavender K. Organic synthesis in deep eutectic solvents: Paal-Knorr reactions Tetrahedron Letters. 54: 4377-4379. DOI: 10.1016/j.tetlet.2013.05.122 |
0.345 |
|
2013 |
Hawkins I, Handy ST. Synthesis of aurones under neutral conditions using a deep eutectic solvent Tetrahedron. 69: 9200-9204. DOI: 10.1016/j.tet.2013.08.060 |
0.318 |
|
2011 |
Bornemann S, Handy ST. Synthetic organic electrochemistry in ionic liquids: the viscosity question. Molecules (Basel, Switzerland). 16: 5963-74. PMID 21769062 DOI: 10.3390/molecules16075963 |
0.383 |
|
2011 |
Bailey L, Handy ST. Aromatic iodination using N-iodosaccharin in room temperature ionic liquids Tetrahedron Letters. 52: 2413-2414. DOI: 10.1016/j.tetlet.2011.03.010 |
0.406 |
|
2010 |
GRIECO PA, COLLINS JL, HANDY ST. ChemInform Abstract: Acid-Catalyzed Ionic Diels-Alder Reactions in Concentrated Solutions of Lithium Perchlorate in Diethyl Ether. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199616051 |
0.344 |
|
2010 |
HANDY ST, GRIECO PA, MINEUR C, GHOSEZ L. ChemInform Abstract: Lithium Trifluoromethanesulfonimide in Acetone or Diethyl Ether as a Safe Alternative to Lithium Perchlorate in Diethyl Ether for Effecting Diels-Alder Reactions. Unexpected Influence of the Counterion on Exo/ Endo Selectivity. Cheminform. 26: no-no. DOI: 10.1002/chin.199539045 |
0.341 |
|
2010 |
GRIECO PA, BECK JP, HANDY ST, SAITO N, DAEUBLE JF. ChemInform Abstract: Acid Catalyzed Intramolecular Diels-Alder Reactions in Lithium Perchlorate-Diethyl Ether: Acid Promoted Migration of Terminal Dienes Prior to (4 + 2) Cycloaddition in Conformationally Restricted Substrates. Cheminform. 26: no-no. DOI: 10.1002/chin.199507061 |
0.349 |
|
2009 |
Ennis E, Handy ST. A facile route to C2-substituted imidazolium ionic liquids. Molecules (Basel, Switzerland). 14: 2235-45. PMID 19553895 DOI: 10.3390/Molecules14062235 |
0.602 |
|
2007 |
Ennis E, Handy ST. The chemistry of the C2 position of imidazolium room temperature ionic liquids Current Organic Synthesis. 4: 381-389. DOI: 10.2174/157017907782408824 |
0.593 |
|
2007 |
Manchanayakage R, Handy ST. Regioselective Barbier reactions of 2-bromomethylcyclohexenone Tetrahedron Letters. 48: 3819-3822. DOI: 10.1016/j.tetlet.2007.03.158 |
0.301 |
|
2007 |
Handy ST, Okello M, Bwambok D. Room temperature ionic liquids as homogeneous supports for synthesis Acs Symposium Series. 950: 116-126. |
0.311 |
|
2006 |
Handy ST. Grignard reactions in imidazolium ionic liquids. The Journal of Organic Chemistry. 71: 4659-62. PMID 16749801 DOI: 10.1021/jo060536o |
0.455 |
|
2006 |
Handy ST, Sabatini JJ. Regioselective dicouplings: application to differentially substituted pyrroles. Organic Letters. 8: 1537-9. PMID 16597104 DOI: 10.1021/ol0530981 |
0.317 |
|
2006 |
Handy ST. One-pot halogenation-Heck coupling reactions in ionic liquids Synlett. 3176-3178. DOI: 10.1055/s-2006-948192 |
0.338 |
|
2006 |
Handy ST, Okello M, Bwambok D. Imidazolium ionic liquids: C2 substitution and acidity Proceedings - Electrochemical Society. 548-555. |
0.493 |
|
2005 |
Handy ST, Okello M. Homogeneous supported synthesis using ionic liquid supports: tunable separation properties. The Journal of Organic Chemistry. 70: 2874-7. PMID 15787592 DOI: 10.1021/jo047807k |
0.327 |
|
2005 |
Handy ST, Okello M. The 2-position of imidazolium ionic liquids: substitution and exchange. The Journal of Organic Chemistry. 70: 1915-8. PMID 15730322 DOI: 10.1021/jo0480850 |
0.436 |
|
2003 |
Handy ST, Okello M, Dickinson G, Dickenson G. Solvents from biorenewable sources: ionic liquids based on fructose. Organic Letters. 5: 2513-5. PMID 12841768 DOI: 10.1021/Ol034778B |
0.482 |
|
2003 |
Handy ST, Okello M. Fructose-derived ionic liquids: Recyclable homogeneous supports Tetrahedron Letters. 44: 8399-8402. DOI: 10.1016/j.tetlet.2003.09.121 |
0.384 |
|
2003 |
Handy ST, Okello M. Halide effects on the Heck reaction in room temperature ionic liquids Tetrahedron Letters. 44: 8395-8397. DOI: 10.1016/j.tetlet.2003.09.120 |
0.448 |
|
2003 |
Handy ST. Greener solvents: Room temperature ionic liquids from biorenewable sources Chemistry - a European Journal. 9: 2938-2944. DOI: 10.1002/chem.200304799 |
0.391 |
|
2002 |
Handy ST, Egrie CR. Green Synthesis: Aromatic Nitrations in Room-Temperature Ionic Liquids Acs Symposium Series. 818: 134-146. |
0.408 |
|
2001 |
Handy ST, Zhang X. Organic synthesis in ionic liquids: The stille coupling Organic Letters. 3: 233-236. PMID 11430042 DOI: 10.1021/ol0068849 |
0.369 |
|
1997 |
Grieco PA, Handy ST. Magnesium trifluoromethanesulfonimide(triflimide) promoted substitution reactions of allylic and benzylic acetates. Magnesium triflimide as a substitute for magnesium perchlorate. Tetrahedron Letters. 38: 2645-2648. DOI: 10.1016/S0040-4039(97)00441-3 |
0.571 |
|
1997 |
Wender PA, Handy ST, Wright DL. Towards the ideal synthesis Chemistry and Industry (London). X-XI. |
0.419 |
|
1995 |
Grieco PA, Collins JL, Handy ST. Acid Catalyzed Ionic Diels-Alder Reactions in Concentrated Solutions of Lithium Perchlorate in Diethyl Ether Synlett. 1995: 1155-1157. DOI: 10.1055/s-1995-5222 |
0.341 |
|
1994 |
Grieco PA, Handy ST, Beck JP. Acid catalyzed intramolecular Diels-Alder reactions in lithium perchlorate-diethyl ether: Enhanced reaction rates and diastereoselectivity Tetrahedron Letters. 35: 2663-2666. DOI: 10.1016/S0040-4039(00)77000-6 |
0.555 |
|
1994 |
Grieco PA, Beck JP, Handy ST, Saito N, Daeuble JF, Campaigne EE, Carmack M. Acid catalyzed intramolecular Diels-Alder reactions in lithium perchlorate-diethyl ether: Acid promoted migration of terminal dienes prior to [4+2] cycloaddition in conformationally restricted substrates Tetrahedron Letters. 35: 6783-6786. DOI: 10.1016/0040-4039(94)85004-6 |
0.551 |
|
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