Year |
Citation |
Score |
2024 |
Benda MC, Evans C, Yuan S, McClish IM, Berkey WJ, Areheart HE, Arnold ES, Tang ML, France S. Modular Enantioselective Total Syntheses of the -7,9-Dihydroxy- and 9-Hydroxy-7-Keto-8,4'-Oxyneolignans. The Journal of Organic Chemistry. PMID 38959240 DOI: 10.1021/acs.joc.4c00710 |
0.418 |
|
2023 |
Evans C, Berkey WJ, Jones CW, France S. Zr-Catalyzed Synthesis of Tetrasubstituted 1,3-Diacylpyrroles from -Acyl α-Aminoaldehydes and 1,3-Dicarbonyls. The Journal of Organic Chemistry. PMID 37294689 DOI: 10.1021/acs.joc.3c00675 |
0.55 |
|
2022 |
Yuan S, Guerra Faura G, Areheart HE, Peulen NE, France S. Lewis Acid-Catalyzed 2,3-Dihydrofuran Acetal Ring-Opening Benzannulations toward Functionalized 1-Hydroxycarbazoles. Molecules (Basel, Switzerland). 27. PMID 36500437 DOI: 10.3390/molecules27238344 |
0.449 |
|
2022 |
Chen D, Jones EV, Williams CW, Huynh TN, McPhail TC, France SA. Intramolecular, Interrupted Homo-Nazarov Cascade Biscyclizations to Angular (Hetero)Aryl-Fused Polycycles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 35700088 DOI: 10.1002/chem.202201368 |
0.395 |
|
2021 |
Guerra Faura G, Nguyen T, France S. Catalyst-Controlled Chemodivergent Reactions of 2-Pyrrolyl-α-diazo-β-ketoesters and Enol Ethers: Synthesis of 1,2-Dihydrofuran Acetals and Highly Substituted Indoles. The Journal of Organic Chemistry. 86: 10088-10104. PMID 34259515 DOI: 10.1021/acs.joc.1c00826 |
0.382 |
|
2020 |
Ronaghi N, Fialho DM, Jones CW, France S. Conversion of Unprotected Aldose Sugars to Polyhydroxyalkyl and -Glycosyl Furans via Zirconium Catalysis. The Journal of Organic Chemistry. PMID 33226804 DOI: 10.1021/acs.joc.0c02176 |
0.805 |
|
2020 |
Benda MC, France S. Chiral disulfonimides: a versatile template for asymmetric catalysis. Organic & Biomolecular Chemistry. PMID 32940322 DOI: 10.1039/d0ob01742f |
0.38 |
|
2019 |
Parker AN, Martin MC, Shenje R, France S. Calcium-Catalyzed Formal [5 + 2] Cycloadditions of Alkylidene β-Ketoesters with Olefins: Chemodivergent Synthesis of Highly Functionalized Cyclohepta[]indole Derivatives. Organic Letters. PMID 31512880 DOI: 10.1021/Acs.Orglett.9B02498 |
0.821 |
|
2018 |
Ward G, Liotta CL, Krishnamurthy R, France S. Base-Mediated Cascade Aldol Addition and Fragmentation Reactions of Dihydroxyfumaric Acid and Aromatic Aldehydes: Controlling Chemodivergence via Choice of Base, Solvent, and Substituents. The Journal of Organic Chemistry. PMID 30223647 DOI: 10.1021/Acs.Joc.8B01867 |
0.412 |
|
2017 |
Sandridge MJ, McLarney BD, Williams CW, France S. α-Alkylidene-γ-butyrolactone Formation via Bi(OTf)3-Catalyzed, Dehydrative, Ring-Opening Cyclizations of Cyclopropyl Carbinols: Understanding Substituent Effects and Predicting E/Z Selectivity. The Journal of Organic Chemistry. PMID 28876932 DOI: 10.1021/acs.joc.7b01706 |
0.42 |
|
2017 |
McLarney BD, Cavitt MA, Donnell TM, Musaev DG, France S. Rh(II) -Catalyzed β-C(sp(2) )-H Alkylation of Enol Ethers, Enamides and Enecarbamates with α-Diazo Dicarbonyl Compounds. Chemistry (Weinheim An Der Bergstrasse, Germany). 23: 1129-1135. PMID 27966244 DOI: 10.1002/Chem.201604518 |
0.796 |
|
2016 |
Williams CW, Shenje R, France S. Catalytic, Interrupted Formal Homo-Nazarov Cyclization with (Hetero)arenes: Access to alpha-(Hetero)aryl Cyclohexanones. The Journal of Organic Chemistry. PMID 27529123 DOI: 10.1021/Acs.Joc.6B01312 |
0.846 |
|
2016 |
Sandridge MJ, France S. Calcium-Catalyzed, Dehydrative, Ring-Opening Cyclizations of Cyclopropyl Carbinols Derived from Donor-Acceptor Cyclopropanes. Organic Letters. 18: 4218-21. PMID 27517711 DOI: 10.1021/acs.orglett.6b01933 |
0.431 |
|
2016 |
Leverett CA, Li G, France S, Padwa A. An IMDAF Cascade Approach Toward the Synthesis of the Alkaloid (+/-)-Minfiensine. The Journal of Organic Chemistry. PMID 27214235 DOI: 10.1021/Acs.Joc.6B00771 |
0.377 |
|
2016 |
Aponte-Guzman J, Phun L, Cavitt M, Taylor JE, Davy JC, France SA. Catalytic, Cascade Ring-Opening Benzannulations of 2,3-Dihydrofuran O,O- and N,O-Acetals. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27136896 DOI: 10.1002/Chem.201601954 |
0.749 |
|
2014 |
Shenje R, Williams CW, Francois KM, France S. Catalysis and chemodivergence in the interrupted, formal homo-Nazarov cyclization using allylsilanes. Organic Letters. 16: 6468-71. PMID 25495709 DOI: 10.1021/Ol503305R |
0.842 |
|
2014 |
Shenje R, Martin MC, France S. A catalytic diastereoselective formal [5+2] cycloaddition approach to azepino[1,2-a]indoles: putative donor-acceptor cyclobutanes as reactive intermediates. Angewandte Chemie (International Ed. in English). 53: 13907-11. PMID 25339510 DOI: 10.1002/Anie.201408429 |
0.848 |
|
2014 |
Aponte-Guzmán J, Taylor JE, Tillman E, France S. Catalytic, formal homo-Nazarov-type cyclizations of alkylidene cyclopropane-1,1-ketoesters: access to functionalized arenes and heteroaromatics. Organic Letters. 16: 3788-91. PMID 25003499 DOI: 10.1021/Ol501676Q |
0.844 |
|
2014 |
Martin MC, Patil DV, France S. Functionalized 4-carboxy- and 4-keto-2,3-dihydropyrroles via Ni(II)-catalyzed nucleophilic amine ring-opening cyclizations of cyclopropanes Journal of Organic Chemistry. 79: 3030-3039. PMID 24601622 DOI: 10.1021/Jo5001059 |
0.838 |
|
2014 |
Orwig SD, Chi PV, Du Y, Hill SE, Cavitt MA, Suntharalingam A, Turnage KC, Dickey CA, France S, Fu H, Lieberman RL. Ligands for glaucoma-associated myocilin discovered by a generic binding assay. Acs Chemical Biology. 9: 517-25. PMID 24279319 DOI: 10.1021/Cb4007776 |
0.747 |
|
2014 |
Cavitt MA, Phun LH, France S. Intramolecular donor-acceptor cyclopropane ring-opening cyclizations. Chemical Society Reviews. 43: 804-18. PMID 24257068 DOI: 10.1039/C3Cs60238A |
0.806 |
|
2012 |
Patil DV, Cavitt MA, Grzybowski P, France S. A general intramolecular Friedel-Crafts approach to functionalized pyrrolo[3,2,1-ij]quinolin-4-ones. Chemical Communications (Cambridge, England). 48: 10337-9. PMID 22968155 DOI: 10.1039/C2Cc34650H |
0.824 |
|
2012 |
Phun LH, Aponte-Guzman J, France S. Indium-catalyzed cycloisomerizations of cyclopropene-3,3-dicarbonyl compounds: efficient access to benzo-fused heteroaromatics and heterobiaryls. Angewandte Chemie (International Ed. in English). 51: 3198-202. PMID 22344854 DOI: 10.1002/Anie.201107717 |
0.775 |
|
2011 |
Patil DV, Cavitt MA, France S. Diastereoselective intramolecular Friedel-Crafts cyclizations of substituted methyl 2-(1H-indole-1-carbonyl)acrylates: efficient access to functionalized 1H-pyrrolo[1,2-a]indoles. Organic Letters. 13: 5820-3. PMID 21988209 DOI: 10.1021/Ol202431X |
0.808 |
|
2011 |
Patil DV, Cavitt MA, Grzybowski P, France S. An efficient synthesis of hydropyrido[1,2-a]indole-6(7H)-ones via an In(III)-catalyzed tandem cyclopropane ring-opening/Friedel-Crafts alkylation sequence. Chemical Communications (Cambridge, England). 47: 10278-80. PMID 21860850 DOI: 10.1039/C1Cc14131G |
0.81 |
|
2011 |
Stout EP, Cervantes S, Prudhomme J, France S, La Clair JJ, Le Roch K, Kubanek J. Bromophycolide A targets heme crystallization in the human malaria parasite Plasmodium falciparum. Chemmedchem. 6: 1572-7. PMID 21732541 DOI: 10.1002/Cmdc.201100252 |
0.646 |
|
2011 |
Phun LH, Patil DV, Cavitt MA, France S. A catalytic homo-Nazarov cyclization protocol for the synthesis of heteroaromatic ring-fused cyclohexanones. Organic Letters. 13: 1952-5. PMID 21417304 DOI: 10.1021/Ol200305N |
0.804 |
|
2010 |
Patil DV, Phun LH, France S. Indium-catalyzed homo-Nazarov cyclizations of alkenyl cyclopropyl ketones. Organic Letters. 12: 5684-7. PMID 21090788 DOI: 10.1021/Ol102497W |
0.803 |
|
2010 |
Liu X, Chan CB, Jang SW, Pradoldej S, Huang J, He K, Phun LH, France S, Xiao G, Jia Y, Luo HR, Ye K. A synthetic 7,8-dihydroxyflavone derivative promotes neurogenesis and exhibits potent antidepressant effect. Journal of Medicinal Chemistry. 53: 8274-86. PMID 21073191 DOI: 10.1021/Jm101206P |
0.766 |
|
2008 |
France S, Boonsombat J, Leverett CA, Padwa A. Cycloaddition across the benzofuran ring as an approach to the morphine alkaloids. The Journal of Organic Chemistry. 73: 8120-3. PMID 18788783 DOI: 10.1021/Jo8016956 |
0.366 |
|
2007 |
Hong X, France S, Padwa A. A Dipolar Cycloaddition Approach Toward the Kopsifoline Alkaloid Framework. Tetrahedron. 63: 5962-5976. PMID 17710185 DOI: 10.1016/J.Tet.2007.01.064 |
0.41 |
|
2006 |
Dogo-Isonagie C, Bekele T, France S, Wolfer J, Weatherwax A, Taggi AE, Lectka T. Scalable methodology for the catalytic, asymmetric alpha-bromination of acid chlorides. The Journal of Organic Chemistry. 71: 8946-9. PMID 17081026 DOI: 10.1021/Jo061522L |
0.796 |
|
2006 |
Hong X, France S, Mejía-Oneto JM, Padwa A. Cycloaddition protocol for the assembly of the hexacyclic framework associated with the kopsifoline alkaloids. Organic Letters. 8: 5141-4. PMID 17048863 DOI: 10.1021/Ol062029Z |
0.344 |
|
2005 |
France S, Bernstein D, Weatherwax A, Lectka T. Performing the synthesis of a complex molecule on sequentially linked columns: toward the development of a "synthesis machine". Organic Letters. 7: 3009-12. PMID 15987192 DOI: 10.1021/Ol050980Y |
0.736 |
|
2005 |
France S, Shah MH, Weatherwax A, Wack H, Roth JP, Lectka T. Bifunctional Lewis acid-nucleophile-based asymmetric catalysis: mechanistic evidence for imine activation working in tandem with chiral enolate formation in the synthesis of beta-lactams. Journal of the American Chemical Society. 127: 1206-15. PMID 15669860 DOI: 10.1021/Ja044179F |
0.817 |
|
2004 |
France S, Weatherwax A, Taggi AE, Lectka T. Advances in the catalytic, asymmetric synthesis of beta-lactams. Accounts of Chemical Research. 37: 592-600. PMID 15311958 DOI: 10.1021/Ar030055G |
0.804 |
|
2004 |
Wack H, France S, Hafez AM, Drury WJ, Weatherwax A, Lectka T. Development of a new dimeric cyclophane ligand: application to enhanced diastereo- and enantioselectivity in the catalytic synthesis of beta-lactams. The Journal of Organic Chemistry. 69: 4531-3. PMID 15202914 DOI: 10.1021/Jo049804D |
0.784 |
|
2004 |
France S, Wack H, Taggi AE, Hafez AM, Wagerle TR, Shah MH, Dusich CL, Lectka T. Catalytic, asymmetric alpha-chlorination of acid halides. Journal of the American Chemical Society. 126: 4245-55. PMID 15053614 DOI: 10.1021/Ja039046T |
0.811 |
|
2003 |
France S, Guerin DJ, Miller SJ, Lectka T. Nucleophilic chiral amines as catalysts in asymmetric synthesis. Chemical Reviews. 103: 2985-3012. PMID 12914489 DOI: 10.1021/Cr020061A |
0.633 |
|
2002 |
France S, Wack H, Hafez AM, Taggi AE, Witsil DR, Lectka T. Bifunctional asymmetric catalysis: a tandem nucleophile/Lewis acid promoted synthesis of beta-lactams. Organic Letters. 4: 1603-5. PMID 11975639 DOI: 10.1021/Ol025805L |
0.81 |
|
2002 |
Taggi AE, Wack H, Hafez AM, France S, Lectka T. Generation of ketenes from acid chlorides using NaH/crown ether shuttle-deprotonation for use in asymmetric catalysis. Organic Letters. 4: 627-9. PMID 11843608 DOI: 10.1021/Ol0172525 |
0.814 |
|
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