Year |
Citation |
Score |
2019 |
Vidhani DV, Alabugin IV. Controlled Evolution of the Cope Rearrangement: Transition from Concerted to Interrupted and Aborted Pericyclic Reactions Regulated by a Switch Built from an Intramolecular Frustrated Lewis Pair. The Journal of Organic Chemistry. PMID 31618028 DOI: 10.1021/Acs.Joc.9B02633 |
0.368 |
|
2016 |
Vidhani DV, Krafft ME, Alabugin IV. Gold(I)-catalyzed allenyl Cope rearrangement: evolution from asynchronicity to trappable intermediates assisted by stereoelectronic switching. Journal of the American Chemical Society. PMID 26850567 DOI: 10.1021/Jacs.5B12920 |
0.591 |
|
2015 |
Vidhani DV, Krafft ME. Proximity effect: insight into the fundamental forces governing chemical reactivity of aromatic systems. The Journal of Physical Chemistry. A. 119: 3141-6. PMID 25714920 DOI: 10.1021/Acs.Jpca.5B00482 |
0.601 |
|
2014 |
Vidhani DV, Krafft ME, Alabugin IV. Rh(I)-catalyzed transformation of propargyl vinyl ethers into (E,Z)-dienals: stereoelectronic role of trans effect in a metal-mediated pericyclic process and a shift from homogeneous to heterogeneous catalysis during a one-pot reaction. The Journal of Organic Chemistry. 79: 352-64. PMID 24304338 DOI: 10.1021/Jo402505F |
0.658 |
|
2014 |
Cran J, Vidhani D, Krafft M. Copper-Catalyzed N-tert-Butylation of Aromatic Amines under Mild Conditions Using tert-Butyl 2,2,2-Trichloroacetimidate Synlett. 25: 1550-1554. DOI: 10.1055/S-0033-1339107 |
0.633 |
|
2014 |
Cran JW, Vidhani DV, Krafft ME. ChemInform Abstract: Copper-Catalyzed N-tert-Butylation of Aromatic Amines under Mild Conditions Using tert-Butyl 2,2,2-Trichloroacetimidate. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201451084 |
0.611 |
|
2013 |
Vidhani DV, Krafft ME, Alabugin IV. Stereocontrolled synthesis of (E,Z)-dienals via tandem Rh(I)-catalyzed rearrangement of propargyl vinyl ethers. Organic Letters. 15: 4462-5. PMID 23968534 DOI: 10.1021/Ol4019985 |
0.608 |
|
2013 |
Vidhani DV, Cran JW, Krafft ME, Alabugin IV. Overriding the alkynophilicity of gold: catalytic pathways from higher energy Au(I)-substrate complexes and reactant deactivation via unproductive complexation in the gold(I)-catalyzed propargyl Claisen rearrangement. Organic & Biomolecular Chemistry. 11: 1624-30. PMID 23307145 DOI: 10.1039/C2Ob27231H |
0.638 |
|
2013 |
Vidhani DV, Cran JW, Krafft ME, Manoharan M, Alabugin IV. Gold(I)-catalyzed Claisen rearrangement of allenyl vinyl ethers: missing transition states revealed through evolution of aromaticity, Au(I) as an oxophilic Lewis acid, and lower energy barriers from a high energy complex. The Journal of Organic Chemistry. 78: 2059-73. PMID 23167800 DOI: 10.1021/Jo302152J |
0.646 |
|
2012 |
Krafft ME, Vidhani DV, Cran JW. ChemInform Abstract: Tributyltin Hydride as a Selective Reducing Agent for Aryl Enones. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201205074 |
0.568 |
|
2011 |
Krafft ME, Hallal KM, Vidhani DV, Cran JW. Gold(I)-catalyzed Claisen rearrangement of allenyl vinyl ethers; synthesis of substituted 1,3-dienes. Organic & Biomolecular Chemistry. 9: 7535-8. PMID 21938297 DOI: 10.1039/C1Ob06297B |
0.577 |
|
2011 |
Krafft ME, Vidhani DV, Cran JW, Manoharan M. Solvent controlled mechanistic dichotomy in a Au(III)-catalyzed, heterocyclization triggered, Nazarov reaction. Chemical Communications (Cambridge, England). 47: 6707-9. PMID 21556413 DOI: 10.1039/C1Cc10920K |
0.664 |
|
2011 |
Krafft M, Vidhani D, Cran J. Tributyltin Hydride as a Selective Reducing Agent for Aryl Enones Synlett. 2011: 2355-2358. DOI: 10.1055/S-0030-1261231 |
0.622 |
|
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