| Year |
Citation |
Score |
| 2016 |
Fu W, Carr PJ, Lecours MJ, Burt M, Marta RA, Steinmetz V, Fillion E, McMahon TB, Hopkins WS. Intramolecular cation-π interactions in protonated phenylalanine derivatives. Physical Chemistry Chemical Physics : Pccp. PMID 27929166 DOI: 10.1039/C6Cp07337A |
0.352 |
|
| 2016 |
Fillion E, Kavoosi A, Nguyen K, Ieritano C. B(C6F5)3-Catalyzed transfer 1,4-hydrostannylation of α,β-unsaturated carbonyls using iPr-tricarbastannatrane. Chemical Communications (Cambridge, England). PMID 27731869 DOI: 10.1039/C6Cc07819B |
0.324 |
|
| 2016 |
Fillion E, Beaton E, Nguyen Y, Wilsily A, Bondarenko G, Jacq J. Facile Hydrogenolysis of C(sp3)-C(sp3) σ Bonds Advanced Synthesis & Catalysis. 358: 3422-3434. DOI: 10.1002/Adsc.201600535 |
0.476 |
|
| 2015 |
Kavoosi A, Fillion E. Synthesis and characterization of tricarbastannatranes and their reactivity in B(C6F5)3-promoted conjugate additions. Angewandte Chemie (International Ed. in English). 54: 5488-92. PMID 25754121 DOI: 10.1002/Anie.201500983 |
0.343 |
|
| 2014 |
Ahmar S, Fillion E. Expedient synthesis of complex γ-butyrolactones from 5-(1-arylalkylidene) meldrum's acids via sequential conjugate alkynylation/Ag(I)-catalyzed lactonization. Organic Letters. 16: 5748-51. PMID 25337888 DOI: 10.1021/Ol502811J |
0.48 |
|
| 2014 |
Hopkins WS, Hasan M, Burt M, Marta RA, Fillion E, McMahon TB. Persistent Intramolecular C-H···X (X = O or S) Hydrogen-Bonding in Benzyl Meldrum's Acid Derivatives. The Journal of Physical Chemistry. A. PMID 24785148 DOI: 10.1021/Jp5029245 |
0.338 |
|
| 2014 |
Lou T, Liao E, Wilsily E, Fillion E. Catalytic Intramolecular Friedel‐Crafts Reaction of Benzyl Meldrum's Acid Derivatives: Preparation of 5,6‐Dimethoxy‐2‐Methyl‐1‐Indanone Organic Syntheses. 115-125. DOI: 10.1002/0471264229.Os089.13 |
0.493 |
|
| 2012 |
Mahoney SJ, Lou T, Bondarenko G, Fillion E. Carbon-based leaving group in substitution reactions: functionalization of sp3-hybridized quaternary and tertiary benzylic carbon centers. Organic Letters. 14: 3474-7. PMID 22697467 DOI: 10.1021/Ol301442Z |
0.481 |
|
| 2012 |
Fillion E, Lou T, Liao ET, Wilsily A. Catalytic intramolecular friedel-crafts reaction of benzyl meldrum's acid derivatives: Preparation of 5,6-dimethoxy-2-methyl-1-indanone Organic Syntheses. 89: 115-125. DOI: 10.15227/orgsyn.089.0115 |
0.382 |
|
| 2010 |
Dumas AM, Fillion E. Meldrum's acids and 5-alkylidene meldrum's acids in catalytic carbon-carbon bond-forming processes Accounts of Chemical Research. 43: 440-454. PMID 20000793 DOI: 10.1021/Ar900229Z |
0.533 |
|
| 2010 |
LAUTENS M, FILLION E, SAMPAT M. ChemInform Abstract: The Effect of the Acidifying Group on the Regioselectivity of the Base-Induced Ring Opening of Hetero-oxabicyclic [3.2.1] and [3.3.1] Systems. Cheminform. 29: no-no. DOI: 10.1002/chin.199822116 |
0.34 |
|
| 2009 |
Mahoney SJ, Dumas AM, Fillion E. Asymmetric addition of alkenylstannanes to alkylidene Meldrum's acids. Organic Letters. 11: 5346-9. PMID 19856944 DOI: 10.1021/Ol902216Y |
0.43 |
|
| 2009 |
Fillion E, Zorzitto AK. Enantioselective rhodium-catalyzed conjugate alkynylation of 5-benzylidene Meldrum's acids with TMS-acetylene Journal of the American Chemical Society. 131: 14608-14609. PMID 19824719 DOI: 10.1021/Ja905336P |
0.487 |
|
| 2009 |
Wilsily A, Fillion E. Asymmetric synthesis of all-carbon benzylic quaternary stereocenters via conjugate addition to alkylidene and indenylidene Meldrum's acids. The Journal of Organic Chemistry. 74: 8583-94. PMID 19824691 DOI: 10.1021/Jo901559D |
0.396 |
|
| 2009 |
Wilsily A, Nguyen Y, Fillion E. Hydrogenolysis of unstrained carbon-carbon sigma bonds: stereoselective entry into benzylic tertiary centers. Journal of the American Chemical Society. 131: 15606-7. PMID 19810747 DOI: 10.1021/ja9076815 |
0.303 |
|
| 2009 |
Dumas AM, Fillion E. Sc(OTf)3-catalyzed conjugate allylation of alkylidene Meldrum's acids. Organic Letters. 11: 1919-22. PMID 19341311 DOI: 10.1021/Ol9003959 |
0.513 |
|
| 2009 |
Fillion E, Wilsily A, Fishlock D. Probing persistent intramolecular C-H...X (X = O, S, Br, Cl, and F) bonding in solution using benzyl Meldrum's acid derivatives. The Journal of Organic Chemistry. 74: 1259-67. PMID 19113820 DOI: 10.1021/Jo802311W |
0.39 |
|
| 2009 |
Wilsily A, Lou T, Fillion E. Enantioselective copper-catalyzed conjugate addition of dimethylzinc to 5-(1-arylalkylidene) Meldrum's acids Synthesis. 2066-2072. DOI: 10.1055/S-0029-1216845 |
0.461 |
|
| 2009 |
Fillion E, Trépanier VE, Heikkinen JJ, Remorova AA, Carson RJ, Goll JM, Seed A. Palladium-catalyzed intramolecular reactions of (E)-2,2-disubstituted 1-alkenyldimethylalanes with aryl triflates Organometallics. 28: 3518-3531. DOI: 10.1021/Om900286X |
0.457 |
|
| 2009 |
Dumas AM, Fillion E. Sc(OTf)3-catalyzed conjugate allylation of alkylidene meldrum's acids Organic Letters. 11: 1919-1922. DOI: 10.1021/ol9003959 |
0.365 |
|
| 2009 |
Mahoney SJ, Moon DT, Hollinger J, Fillion E. Functionalization of Csp3-H bond-Sc(OTf)3-catalyzed domino 1,5-hydride shift/cyclization/Friedel-Crafts acylation reaction of benzylidene Meldrum's acids Tetrahedron Letters. 50: 4706-4709. DOI: 10.1016/J.Tetlet.2009.06.007 |
0.486 |
|
| 2009 |
Fillion E, Fishlock D. Scandium triflate-catalyzed intramolecular Friedel-Crafts acylation with Meldrum's acids: insight into the mechanism Tetrahedron. 65: 6682-6695. DOI: 10.1016/J.Tet.2009.05.058 |
0.447 |
|
| 2008 |
Wilsily A, Fillion E. Asymmetric synthesis of carboxylic acid derivatives having an all-carbon alpha-quaternary center through Cu-catalyzed 1,4-addition of dialkylzinc reagents to 2-aryl acetate derivatives. Organic Letters. 10: 2801-4. PMID 18510334 DOI: 10.1021/Ol800923Q |
0.466 |
|
| 2008 |
Fillion E, Dumas AM. Synthesis of fused 4,5-disubstituted indole ring systems by intramolecular friedel-crafts acylation of 4-substituted indoles Journal of Organic Chemistry. 73: 2920-2923. PMID 18321122 DOI: 10.1021/Jo702591P |
0.416 |
|
| 2008 |
Fillion E, Carret S, Mercier LG, Trépanier VE. Sequential Rh(l)/Pd-catalyzed 1,4-addition/Lntramolecular allylation: Stereocontrolled construction of γ-butyrolactones and cyclopropanes Organic Letters. 10: 437-440. PMID 18183992 DOI: 10.1021/Ol702613F |
0.416 |
|
| 2008 |
Goll JM, Fillion E. Tuning the reactivity of palladium carbenes derived from diphenylketene Organometallics. 27: 3622-3625. DOI: 10.1021/Om800390W |
0.361 |
|
| 2007 |
Trépanier VE, Fillion E. Ambiphilic vinylcarbenoid reactivity of (α-(tributylstannyl)-,π- allyl)palladium(II) species Organometallics. 26: 30-32. DOI: 10.1021/Om0609416 |
0.385 |
|
| 2007 |
Dumas AM, Seed A, Zorzitto AK, Fillion E. A general and practical preparation of alkylidene Meldrum's acids Tetrahedron Letters. 48: 7072-7074. DOI: 10.1016/J.Tetlet.2007.08.012 |
0.444 |
|
| 2006 |
Fillion E, Dumas AM, Hogg SA. Modular synthesis of tetrahydrofluorenones from 5-alkylidene Meldrum's acids Journal of Organic Chemistry. 71: 9899-9902. PMID 17168619 DOI: 10.1021/Jo0618876 |
0.5 |
|
| 2006 |
Fillion E, Wilsily A. Asymmetric synthesis of all-carbon benzylic quaternary stereocenters via Cu-catalyzed conjugate addition of dialkylzinc reagents to 5-(1-arylalkylidene) Meldrum's acids. Journal of the American Chemical Society. 128: 2774-5. PMID 16506736 DOI: 10.1021/Ja056692E |
0.47 |
|
| 2006 |
Fillion E, Dumas AM, Kuropatwa BA, Malhotra NR, Sitler TC. Yb(OTf)3-catalyzed reactions of 5-alkylidene Meldrum's acids with phenols: One-pot assembly of 3,4-dihydrocoumarins, 4-chromanones, coumarins, and chromones Journal of Organic Chemistry. 71: 409-412. PMID 16388672 DOI: 10.1021/Jo052000T |
0.49 |
|
| 2006 |
Fillion E, Wilsily A, Liao ET. Asymmetric Cu-catalyzed 1,6-conjugate addition of dialkylzinc reagents to 5-(3-aryl-2-propenylidene) Meldrum's acids Tetrahedron Asymmetry. 17: 2957-2959. DOI: 10.1016/J.Tetasy.2006.11.009 |
0.428 |
|
| 2005 |
Fillion E, Fishlock D. Total synthesis of (±)-Taiwaniaquinol B via a domino intramolecular Friedel-Crafts acylation/carbonyl α-tert-alkylation reaction Journal of the American Chemical Society. 127: 13144-13145. PMID 16173732 DOI: 10.1021/Ja054447P |
0.483 |
|
| 2005 |
Fillion E, Fishlock D, Wilsily A, Goll JM. Meldrum's acids as acylating agents in the catalytic intramolecular Friedel-Crafts reaction. The Journal of Organic Chemistry. 70: 1316-27. PMID 15704966 DOI: 10.1021/Jo0483724 |
0.518 |
|
| 2005 |
Fillion E, Trépanier VE, Mercier LG, Remorova AA, Carson RJ. Oxidative coupling of 2-substituted 1,2-dihydro-1-naphthols using Jones reagent: A simple entry into 3,3′-disubstituted 1,1′-binaphthyl-4, 4′-diols Tetrahedron Letters. 46: 1091-1094. DOI: 10.1016/J.Tetlet.2004.12.099 |
0.354 |
|
| 2004 |
Fillion E, Carson RJ, Trépanier VE, Goll JM, Remorova AA. Palladium-catalyzed carbon-carbon bond-forming 1,2-ligand migration of organoalanes. Journal of the American Chemical Society. 126: 15354-5. PMID 15563142 DOI: 10.1021/Ja045783T |
0.403 |
|
| 2003 |
Fillion E, Beingessner RL. Enantioselective Synthesis of Bicyclo[6.1.0]nonane-9-carboxylic Acids via Me2AlOTf-Promoted Intramolecular Friedel-Crafts Alkylation of Arenes with the γ-Lactone Moiety of 3-Oxabicyclo[3.1.0]hexan-2-ones Journal of Organic Chemistry. 68: 9485-9488. PMID 14629177 DOI: 10.1021/Jo0351419 |
0.485 |
|
| 2003 |
Fillion E, Fishlock D. Convenient access to polysubstituted 1-indanones by Sc(OTf)3-catalyzed intramolecular Friedel-Crafts acylation of benzyl Meldrum's acid derivatives. Organic Letters. 5: 4653-6. PMID 14627407 DOI: 10.1021/Ol035817M |
0.503 |
|
| 2003 |
Fillion E, Taylor NJ. Cine-substitution in the Stille coupling: evidence for the carbenoid reactivity of sp3-gem-organodimetallic iodopalladio-trialkylstannylalkane intermediates. Journal of the American Chemical Society. 125: 12700-1. PMID 14558805 DOI: 10.1021/Ja037409J |
0.342 |
|
| 2003 |
Fillion E, Fishlock D. Convenient Access to Polysubstituted 1-Indanones by Sc(OTf) 3-Catalyzed Intramolecular Friedel-Crafts Acylation of Benzyl Meldrum's Acid Derivatives Organic Letters. 5: 4653-4656. DOI: 10.1021/ol035817m |
0.398 |
|
| 1998 |
Lautens M, Fillion E. Exploring the Reactivity of Dioxacyclic Compounds as a Route to Polysubstituted Decalins and Fused Polycycles. The Journal of Organic Chemistry. 63: 647-656. PMID 11672056 DOI: 10.1021/Jo971567+ |
0.434 |
|
| 1998 |
Lautens M, Fillion E, Sampat M. The effect of the acidifying group on the regioselectivity of the base-induced ring opening of hetero-oxabicyclic [3.2.1] and [3.3.1] systems Tetrahedron Letters. 39: 1501-1504. DOI: 10.1016/S0040-4039(98)00052-5 |
0.392 |
|
| 1997 |
Lautens M, Fillion E, Sampat M. Base-Induced Ring Opening of Aza- and Thiaoxa[3.2.1] and -[3.3.1]bicycles as an Enantioselective Approach to Azepines, Thiepines, and Thiocines. The Journal of Organic Chemistry. 62: 7080-7081. PMID 11671802 DOI: 10.1021/Jo971474S |
0.342 |
|
| 1997 |
Lautens M, Fillion E. An Expedient Route for the Stereoselective Construction of Bridged Polyheterocyclic Ring Systems Using the Tandem "Pincer" Diels-Alder Reaction. The Journal of Organic Chemistry. 62: 4418-4427. PMID 11671769 DOI: 10.1021/Jo9701593 |
0.454 |
|
| 1996 |
Lautens M, Fillion E. New Strategy for the Stereocontrolled Construction of Decalins and Fused Polycycles via a Tandem Diels-Alder Ring-Opening Sequence. The Journal of Organic Chemistry. 61: 7994-7995. PMID 11667775 DOI: 10.1021/Jo961635C |
0.315 |
|
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