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Kahar NM, Jadhav PP, Dawande SG. (2023) Rhodium(II)-catalyzed synthesis of 2-aminoquinoline derivatives from 2-quinolones and -sulfonyl-1,2,3-triazoles. Organic & Biomolecular Chemistry. 21: 8267-8272
Nabar KU, Bhanage BM, Dawande SG. (2023) Copper-catalyzed -arylation of amines with aryliodonium ylides in water. Beilstein Journal of Organic Chemistry. 19: 1008-1014
Jadhav PP, Kahar NM, Dawande SG. (2021) Ruthenium(II)-Catalyzed Highly Chemo- and Regioselective Oxidative C6 Alkenylation of Indole-7-carboxamides. Organic Letters. 23: 8673-8677
Kahar N, Jadhav P, Reddy RVR, et al. (2020) A rhodium(ii) catalysed domino synthesis of azepino fused diindoles from isatin tethered N-sulfonyl-1,2,3-triazoles and indoles. Chemical Communications (Cambridge, England)
Jadhav PP, Kahar NM, Dawande SG. (2019) Ruthenium(II) Catalysed Highly Regioselective C-3 Alkenylation of Indolizines and Pyrrolo[1,2-a ]quinolines European Journal of Organic Chemistry. 2019: 7831-7835
Kahar NM, Nabar KU, Jadhav PP, et al. (2018) Rhodium(II)-Catalyzed Highly Stereoselective C3 Functionalization of Indolizines with N -Sulfonyl-1,2,3-triazoles Asian Journal of Organic Chemistry. 8: 79-82
Dawande SG, Harode M, Kalepu J, et al. (2016) Ag(i)-catalyzed intramolecular transannulation of enynone tethered donor-acceptor cyclopropanes: a new synthesis of 2,3-dihydronaphtho[1,2-b]furans. Chemical Communications (Cambridge, England). 52: 13699-13701
Dawande SG, Lad BS, Prajapati S, et al. (2016) Rhodium-catalyzed pyridannulation of indoles with diazoenals: a direct approach to pyrido[1,2-a]indoles. Organic & Biomolecular Chemistry
Dawande SG, Kanchupalli V, Lad BS, et al. (2014) Synergistic rhodium(II) carboxylate and brønsted acid catalyzed multicomponent reactions of enalcarbenoids: direct synthesis of α-pyrrolylbenzylamines. Organic Letters. 16: 3700-3
Dawande SG, Kanchupalli V, Kalepu J, et al. (2014) Rhodium enalcarbenoids: direct synthesis of indoles by rhodium(II)-catalyzed [4+2] benzannulation of pyrroles. Angewandte Chemie (International Ed. in English). 53: 4076-80
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