Dipak vachhani - Publications

Affiliations: 
LABORATORY OF ORGANIC AND MICROWAVE ASSISTED CHEMISTRY Katholieke Universiteit Leuven, Leuven, Vlaanderen, Belgium 

34 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Singh S, Butani HH, Vachhani DD, Shah A, Van der Eycken EV. Ruthenium-catalysed one-pot regio- and diastereoselective synthesis of pyrrolo[1,2-a]indoles via cascade C-H functionalization/annulation. Chemical Communications (Cambridge, England). PMID 28920982 DOI: 10.1039/C7Cc06276A  0.695
2015 Vachhani DD, Butani HH, Sharma N, Bhoya UC, Shah AK, Van der Eycken EV. Domino Heck/borylation sequence towards indolinone-3-methyl boronic esters: trapping of the σ-alkylpalladium intermediate with boron. Chemical Communications (Cambridge, England). 51: 14862-5. PMID 26300449 DOI: 10.1039/c5cc05193b  0.701
2015 Sharma UK, Sharma N, Vachhani DD, Van der Eycken EV. Metal-mediated post-Ugi transformations for the construction of diverse heterocyclic scaffolds. Chemical Society Reviews. 44: 1836-60. PMID 25652577 DOI: 10.1039/c4cs00253a  0.602
2015 Vachhani DD, Kumar A, Modha SG, Sharma SK, Parmar VS, Van Der Eycken EV. Diversely substituted indoloazepinones and indoloazocinones: A post-ugi gold-catalyzed regioselective carbocyclization approach Synthesis (Germany). 47: 1337-1347. DOI: 10.1055/S-0034-1379894  0.778
2015 Butani HH, Vachhani DD, Bhoya UC, Shah AK, Van der Eycken EV. Remote Amide-Controlled Gold-Catalyzed Stereoselective Hydro-heteroarylation of Acrylamides: Access to Pyrido[3,4-b]indoles European Journal of Organic Chemistry. 2015: 2124-2128. DOI: 10.1002/EJOC.201403682  0.587
2015 Vachhani DD, Kumar A, Modha SG, Sharma SK, Parmar VS, Van der Eycken EV. ChemInform Abstract: Diversely Substituted Indoloazepinones and Indoloazocinones: A Post-Ugi Gold-Catalyzed Regioselective Carbocyclization Approach. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201539161  0.46
2015 Butani HH, Vachhani DD, Bhoya UC, Shah AK, Van der Eycken EV. ChemInform Abstract: Remote Amide-Controlled Gold-Catalyzed Stereoselective Hydro-Heteroarylation of Acrylamides: Access to Pyrido[3,4-b]indoles. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201530215  0.592
2015 Butani HH, Vachhani DD, Bhoya UC, Shah AK, Van der Eycken EV. ChemInform Abstract: Regio- and Chemoselective Formation of Spiroindolinone-Isoindolinone by a Palladium-Catalyzed Buchwald-Hartwig Addition-Elimination Sequence. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201514121  0.591
2015 Li Z, Kumar A, Vachhani DD, Sharma SK, Parmar VS, Van der Eycken EV. ChemInform Abstract: Regioselective Synthesis of Diversely Substituted Diazoninones Through a Post-Ugi Gold-Catalyzed Intramolecular Hydroarylation Process. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201505192  0.428
2014 Ambasana PA, Vachhani DD, Galli M, Jacobs J, Van Meervelt L, Shah AK, Van der Eycken EV. Solvent switchable cycloaddition: a (one-pot) metal-free approach towards N-substituted benzo[e]- or [f]isoindolones via C(sp(2))-H functionalization. Organic & Biomolecular Chemistry. 12: 8861-5. PMID 25257733 DOI: 10.1039/c4ob01644k  0.676
2014 Li Z, Legras L, Kumar A, Vachhani DD, Sharma SK, Parmar VS, Van der Eycken EV. Microwave-assisted synthesis of 4H-benzo[f]imidazo[1,4]diazepin-6-ones via a post-Ugi copper-catalyzed intramolecular Ullmann coupling Tetrahedron Letters. 55: 2070-2074. DOI: 10.1016/J.TETLET.2014.02.023  0.385
2014 Butani HH, Vachhani DD, Bhoya UC, Shah AK, Van der Eycken EV. Regio- and Chemoselective Formation of Spiroindolinone-Isoindolinone by a Palladium-Catalyzed Buchwald-Hartwig Addition-Elimination Sequence European Journal of Organic Chemistry. 2014: 6634-6638. DOI: 10.1002/EJOC.201402909  0.586
2014 Li Z, Kumar A, Vachhani DD, Sharma SK, Parmar VS, Van der Eycken EV. Regioselective Synthesis of Diversely Substituted Diazoninones Through a Post-Ugi Gold-Catalyzed Intramolecular Hydroarylation Process European Journal of Organic Chemistry. 2014: 2084-2091. DOI: 10.1002/EJOC.201301507  0.428
2014 Li Z, Legras L, Kumar A, Vachhani DD, Sharma SK, Parmar VS, Van der Eycken EV. ChemInform Abstract: Microwave-Assisted Synthesis of 4H-Benzo[f]imidazo[1,4]diazepin-6-ones via a Post-Ugi Copper-Catalyzed Intramolecular Ullmann Coupling. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201436187  0.389
2014 Kumar A, Vachhani DD, Modha SG, Sharma SK, Parmar VS, Van der Eycken EV. ChemInform Abstract: Post Ugi Gold(I)- and Platinum(II)-Catalyzed Alkyne Activation: Synthesis of Diversely Substituted Fused Azepinones and Pyridones. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201407204  0.389
2013 Kumar A, Vachhani DD, Modha SG, Sharma SK, Parmar VS, Van der Eycken EV. Post-Ugi gold-catalyzed diastereoselective domino cyclization for the synthesis of diversely substituted spiroindolines. Beilstein Journal of Organic Chemistry. 9: 2097-102. PMID 24204421 DOI: 10.3762/Bjoc.9.246  0.798
2013 Vachhani DD, Galli M, Jacobs J, Van Meervelt L, Van der Eycken EV. Synthesis of (spiro)cyclopentapyridinones via C(sp3)-H functionalization: a post-Ugi gold-catalyzed regioselective tandem cyclization. Chemical Communications (Cambridge, England). 49: 7171-3. PMID 23831954 DOI: 10.1039/c3cc43418d  0.668
2013 Vachhani DD, Sharma A, Van der Eycken E. Copper-catalyzed direct secondary and tertiary C-H alkylation of azoles through a heteroarene-amine-aldehyde/ketone coupling reaction. Angewandte Chemie (International Ed. in English). 52: 2547-50. PMID 23341157 DOI: 10.1002/Anie.201209312  0.737
2013 Kumar A, Vachhani DD, Modha SG, Sharma SK, Parmar VS, Eycken EVVd. Post Ugi Gold(I)- and Platinum(II)-Catalyzed Alkyne Activation: Synthesis of Diversely Substituted Fused Azepinones and Pyridinones Synthesis. 45: 2571-2582. DOI: 10.1055/S-0033-1339474  0.793
2013 Hooyberghs G, De Coster H, Vachhani DD, Ermolat'ev DS, Van der Eycken EV. Synthesis of [1,2,3]-triazolo[1,5-a][1,4]benzodiazepines via an unprecedented one-pot Cu-catalyzed azidation–cyclization reaction Tetrahedron. 69: 4331-4337. DOI: 10.1016/J.TET.2013.03.031  0.352
2013 Vachhani D, Modha S, Sharma A, Eycken EVd. A facile diversity-oriented synthesis of imidazo[1,2-a]pyrazinones via gold-catalyzed regioselective heteroannulation of propynylaminopyrazinones Tetrahedron. 69: 359-365. DOI: 10.1016/J.Tet.2012.10.019  0.805
2013 Kumar A, Vachhani DD, Modha SG, Sharma SK, Parmar VS, Eycken EVVd. Gold(I)‐Catalyzed Post‐Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles European Journal of Organic Chemistry. 2013: 2288-2292. DOI: 10.1002/Ejoc.201300132  0.789
2013 Vachhani DD, Kumar A, Modha SG, Sharma SK, Parmar VS, Eycken EVVd. Diversely Substituted Triazolo[1,5‐a][1,4]benzodiazepinones: A Post‐Ugi Copper‐Catalyzed Tandem Azide–Alkyne Cycloaddition/Ullmann C–N Coupling Approach European Journal of Organic Chemistry. 2013: 1223-1227. DOI: 10.1002/Ejoc.201201587  0.721
2013 Mishra NM, Vachhani DD, Modha SG, Eycken EVVd. Diversely Substituted Imidazo[1,2-a]pyrazine-8-oxo-3-carbaldehydes: An Iodine-Mediated Cyclization/Oxidation Approach European Journal of Organic Chemistry. 2013: 693-700. DOI: 10.1002/Ejoc.201201150  0.768
2013 Hooyberghs G, De Coster H, Vachhani DD, Ermolat'ev DS, Van der Eycken EV. ChemInform Abstract: Synthesis of [1,2,3]-Triazolo[1,5-a][1,4]benzodiazepines via an Unprecedented One-Pot Cu-Catalyzed Azidation-Cyclization Reaction. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201338174  0.38
2013 Kumar A, Vachhani DD, Modha SG, Sharma SK, Parmar VS, Van der Eycken EV. ChemInform Abstract: Gold(I)-Catalyzed Post-Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201338173  0.357
2013 Vachhani DD, Kumar A, Modha SG, Sharma SK, Parmar VS, Van der Eycken EV. ChemInform Abstract: Diversely Substituted Triazolo[1,5-a][1,4]benzodiazepinones: A Post-Ugi Copper-Catalyzed Tandem Azide-Alkyne Cycloaddition/Ullmann C-N Coupling Approach. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201335168  0.402
2012 Modha SG, Kumar A, Vachhani DD, Sharma SK, Parmar VS, Van der Eycken EV. Gold(I) and platinum(II) switch: a post-Ugi intramolecular hydroarylation to pyrrolopyridinones and pyrroloazepinones. Chemical Communications (Cambridge, England). 48: 10916-8. PMID 23032641 DOI: 10.1039/C2Cc35900F  0.782
2012 Vachhani DD, Sharma A, Van der Eycken E. Pd/Cu-catalyzed C-H arylation of 1,3,4-thiadiazoles with (hetero)aryl iodides, bromides, and triflates. The Journal of Organic Chemistry. 77: 8768-74. PMID 22957511 DOI: 10.1021/Jo301401Q  0.7
2012 Modha SG, Kumar A, Vachhani DD, Jacobs J, Sharma SK, Parmar VS, Van Meervelt L, Van der Eycken EV. A diversity-oriented approach to spiroindolines: post-Ugi gold-catalyzed diastereoselective domino cyclization. Angewandte Chemie (International Ed. in English). 51: 9572-5. PMID 22907654 DOI: 10.1002/Anie.201205052  0.801
2012 Modha SG, Vachhani DD, Jacobs J, Van Meervelt L, Van der Eycken EV. A concise route to indoloazocines via a sequential Ugi-gold-catalyzed intramolecular hydroarylation. Chemical Communications (Cambridge, England). 48: 6550-2. PMID 22622200 DOI: 10.1039/C2Cc32586A  0.816
2012 Sharma A, Vachhani D, Van der Eycken E. Direct heteroarylation of tautomerizable heterocycles into unsymmetrical and symmetrical biheterocycles via Pd/Cu-catalyzed phosphonium coupling. Organic Letters. 14: 1854-7. PMID 22416815 DOI: 10.1021/Ol300455E  0.644
2012 Vachhani DD, Mehta VP, Modha SG, Van Hecke K, Van Meervelt L, Van der Eycken EV. ChemInform Abstract: Microwave-Assisted Synthesis of Pyrazino[2,1-b]quinazolines and 3-Indolyl-2(1H)-pyrazinones Employing a Chemoselective Silver(I)- and Gold(I)-Catalyzed Reaction. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201241176  0.454
2012 Vachhani DD, Mehta VP, Modha SG, Hecke KV, VanMeervelt L, Eycken EVVd. Microwave‐Assisted Synthesis of Pyrazino[2,1‐b]quinazolines and 3‐Indolyl‐2(1H)‐pyrazinones Employing a Chemoselective Silver(I)‐ and Gold(I)‐Catalyzed Reaction Advanced Synthesis & Catalysis. 354: 1593-1599. DOI: 10.1002/Adsc.201100881  0.768
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