Year |
Citation |
Score |
2021 |
Chanson A, Moreau CS, Duplais C. Assessing Biosynthetic Gene Cluster Diversity of Specialized Metabolites in the Conserved Gut Symbionts of Herbivorous Turtle Ants. Frontiers in Microbiology. 12: 678100. PMID 34267736 DOI: 10.3389/fmicb.2021.678100 |
0.605 |
|
2020 |
Birer C, Moreau CS, Tysklind N, Zinger L, Duplais C. Disentangling the assembly mechanisms of ant cuticular bacterial communities of two Amazonian ant species sharing a common arboreal nest. Molecular Ecology. PMID 32133714 DOI: 10.1111/Mec.15400 |
0.703 |
|
2017 |
Birer C, Tysklind N, Zinger L, Duplais C. Comparative analysis of DNA extraction methods to study the body surface microbiota of insects: A case study with ant cuticular bacteria. Molecular Ecology Resources. PMID 28477337 DOI: 10.1111/1755-0998.12688 |
0.705 |
|
2015 |
Leba LJ, Musset L, Pelleau S, Estevez Y, Birer C, Briolant S, Witkowski B, Ménard D, Delves MJ, Legrand E, Duplais C, Popovici J. Use of Plasmodium falciparum culture-adapted field isolates for in vitro exflagellation-blocking assay. Malaria Journal. 14: 234. PMID 26040313 DOI: 10.1186/S12936-015-0752-X |
0.693 |
|
2012 |
Lipshutz BH, Taft BR, Abela AR, Ghorai S, Krasovskiy A, Duplais C. Catalysis in the Service of Green Chemistry: Nobel Prize-Winning Palladium-Catalysed Cross-Couplings, Run in Water at Room Temperature: Heck, Suzuki-Miyaura and Negishi reactions carried out in the absence of organic solvents, enabled by micellar catalysis. Platinum Metals Review. 56: 62-74. PMID 23555153 DOI: 10.1595/147106712X629761 |
0.739 |
|
2011 |
Duplais C, Krasovskiy A, Lipshutz BH. Organozinc Chemistry Enabled by Micellar Catalysis. Palladium-Catalyzed Cross-Couplings between Alkyl and Aryl Bromides in Water at Room Temperature. Organometallics. 30: 6090-6097. PMID 23539206 DOI: 10.1021/Om200846H |
0.596 |
|
2011 |
Lipshutz BH, Ghorai S, Abela AR, Moser R, Nishikata T, Duplais C, Krasovskiy A, Gaston RD, Gadwood RC. TPGS-750-M: a second-generation amphiphile for metal-catalyzed cross-couplings in water at room temperature. The Journal of Organic Chemistry. 76: 4379-91. PMID 21548658 DOI: 10.1021/Jo101974U |
0.767 |
|
2011 |
Krasovskiy A, Thomé I, Graff J, Krasovskaya V, Konopelski P, Duplais C, Lipshutz BH. Cross-couplings of alkyl halides with heteroaromatic halides, in water at room temperature Tetrahedron Letters. 52: 2203-2205. DOI: 10.1016/J.Tetlet.2010.11.160 |
0.563 |
|
2011 |
Krasovskiy A, Thome I, Graff J, Krasovskaya V, Konopelski P, Duplais C, Lipshutz BH. ChemInform Abstract: Cross-Coupling of Alkyl Halides with Heteroaromatic Halides, in Water at Room Temperature. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201130093 |
0.521 |
|
2011 |
Lipshutz BH, Abela AR, Boskovic ZV, Nishikata T, Duplais C, Krasovskiy A. ChemInform Abstract: “Greening Up” Cross-Coupling Chemistry Cheminform. 42: no-no. DOI: 10.1002/chin.201105250 |
0.738 |
|
2010 |
Krasovskiy A, Duplais C, Lipshutz BH. Stereoselective Negishi-like couplings between alkenyl and alkyl halides in water at room temperature. Organic Letters. 12: 4742-4. PMID 20882969 DOI: 10.1021/Ol101885T |
0.572 |
|
2010 |
Duplais C, Forman AJ, Baker BA, Lipshutz BH. UC Pd: a new form of Pd/C for Sonogashira couplings. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 3366-71. PMID 20140914 DOI: 10.1002/Chem.200902471 |
0.476 |
|
2010 |
Duplais C, Krasovskiy A, Wattenberg A, Lipshutz BH. Cross-couplings between benzylic and aryl halides "on water": synthesis of diarylmethanes. Chemical Communications (Cambridge, England). 46: 562-4. PMID 20062862 DOI: 10.1039/B922280D |
0.591 |
|
2010 |
Duplais C, Forman AJ, Baker BA, Lipshutz BH. Sonogashira Coupling with UC Pd under Copper-Free Conditions Synfacts. 2010: 729-729. DOI: 10.1055/S-0029-1219898 |
0.489 |
|
2010 |
Lipshutz BH, Abela AR, Boškovi? ZV, Nishikata T, Duplais C, Krasovskiy A. "Greening up" cross-coupling chemistry Topics in Catalysis. 53: 985-990. DOI: 10.1007/S11244-010-9537-1 |
0.783 |
|
2009 |
Krasovskiy A, Duplais C, Lipshutz BH. Zn-mediated, Pd-catalyzed cross-couplings in water at room temperature without prior formation of organozinc reagents. Journal of the American Chemical Society. 131: 15592-3. PMID 19827762 DOI: 10.1021/Ja906803T |
0.573 |
|
2009 |
Cahiez G, Duplais C, Buendia J. Manganese-catalyzed oxidative cross-coupling of Grignard reagents with oxygen as an oxidant. Angewandte Chemie (International Ed. in English). 48: 6731-4. PMID 19662667 DOI: 10.1002/Anie.200902188 |
0.55 |
|
2009 |
Cahiez G, Duplais C, Buendia J. Chemistry of organomanganese(II) compounds. Chemical Reviews. 109: 1434-76. PMID 19209933 DOI: 10.1021/Cr800341A |
0.485 |
|
2009 |
Cahiez G, Chaboche C, Duplais C, Moyeux A. A new efficient catalytic system for the chemoselective cobalt-catalyzed cross-coupling of aryl Grignard reagents with primary and secondary alkyl bromides. Organic Letters. 11: 277-80. PMID 19093805 DOI: 10.1021/Ol802362E |
0.611 |
|
2009 |
Cahiez G, Chaboche C, Duplais C, Moyeux A. Efficient Cobalt-Catalyzed Coupling of Aryl Grignard Reagentswith Alkyl Bromides Synfacts. 2009: 425-425. DOI: 10.1055/S-0028-1087824 |
0.414 |
|
2009 |
Cahiez G, Duplais C. Iron‐Catalyzed Reactions of Grignard Reagents Patai's Chemistry of Functional Groups. 595-630. DOI: 10.1002/9780470682531.Pat0412 |
0.611 |
|
2008 |
Cahiez G, Chaboche C, Duplais C, Giulliani A, Moyeux A. ChemInform Abstract: Cobalt-Catalyzed Cross-Coupling Reaction Between Functionalized Primary and Secondary Alkyl Halides and Aliphatic Grignard Reagents. Cheminform. 39. DOI: 10.1002/CHIN.200843065 |
0.597 |
|
2008 |
Cahiez G, Chaboche C, Duplais C, Giulliani A, Moyeux A. Cobalt‐Catalyzed Cross‐Coupling Reaction between Functionalized Primary and Secondary Alkyl Halides and Aliphatic Grignard Reagents Advanced Synthesis & Catalysis. 350: 1484-1488. DOI: 10.1002/Adsc.200800166 |
0.602 |
|
2007 |
Cahiez G, Moyeux A, Buendia J, Duplais C. Manganese- or iron-catalyzed homocoupling of grignard reagents using atmospheric oxygen as an oxidant. Journal of the American Chemical Society. 129: 13788-9. PMID 17944469 DOI: 10.1021/Ja075417K |
0.557 |
|
2007 |
Cahiez G, Duplais C, Moyeux A. Iron-catalyzed alkylation of alkenyl Grignard reagents. Organic Letters. 9: 3253-4. PMID 17655319 DOI: 10.1021/Ol7016092 |
0.599 |
|
2007 |
Cahiez G, Habiak V, Duplais C, Moyeux A. Iron-catalyzed alkylations of aromatic grignard reagents. Angewandte Chemie (International Ed. in English). 46: 4364-6. PMID 17465438 DOI: 10.1055/S-2007-968740 |
0.543 |
|
2007 |
Cahiez G, Duplais C, Moyeux A. Iron-Catalyzed Cross-Coupling Reaction Between Alkenyl Grignard Reagents and Alkyl Halides Synfacts. 2007: 1197-1197. DOI: 10.1055/S-2007-991226 |
0.439 |
|
2004 |
Duplais C, Bures F, Sapountzis I, Korn TJ, Cahiez G, Knochel P. An efficient synthesis of diaryl ketones by iron-catalyzed arylation of aroyl cyanides. Angewandte Chemie (International Ed. in English). 43: 2968-70. PMID 15170318 DOI: 10.1002/Anie.200453696 |
0.596 |
|
2004 |
Duplais C, Bures F, Sapountzis I, Korn TJ, Cahiez G, Knochel P. Eine effiziente Synthese von polyfunktionalisierten Diarylketonen durch Eisen-katalysierte Arylierung von Aroylcyaniden Angewandte Chemie. 116: 3028-3030. DOI: 10.1002/Ange.200453696 |
0.536 |
|
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