2020
194. Cu-TEMPO Catalyzed Dehydrogenative Friedlander Annulation/ sp3 C-H functionalization/spiroanulation towards spiro[indoline-3,3'-pyrrolizin]-2'-yl)-4-phenylquinoline-3-carboxylates.
194. Cu-TEMPO Catalyzed Dehydrogenative Friedlander Annulation/ sp3 C-H functionalization/spiroanulation towards spiro[indoline-3,3'-pyrrolizin]-2'-yl)-4-phenylquinoline-3-carboxylates.
Dalavai Pavithra, K. R. Ethiraj, Fazlur Rahman Nawaz Khan* European Journal of Organic Chemistry, 2020,2020, 7035-7050 (Impact factor: 3.261 [Link]
Dalavai Pavithra, K. R. Ethiraj, Fazlur Rahman Nawaz Khan* European Journal of Organic Chemistry, 2020,2020, 7035-7050 (Impact factor: 3.261 [Link]
193. Radical Transformations towards the Synthesis of Quinoline: A review
193. Radical Transformations towards the Synthesis of Quinoline: A review
Chitrala Teja; Fazlur-Rahman Nawaz Khan, Chemistry- An Asian Journal 15, 2020, 4153-4167 (Impact factor: 4.839) [Link]
Chitrala Teja; Fazlur-Rahman Nawaz Khan, Chemistry- An Asian Journal 15, 2020, 4153-4167 (Impact factor: 4.839) [Link]
192. Recent Advances in the Synthesis of Thienoquinolines (Quinoline‐fused heterocycle)
192. Recent Advances in the Synthesis of Thienoquinolines (Quinoline‐fused heterocycle)
Chitrala Teja, Fazlur-Rahman Nawaz Khan, Asian Journal of Organic Chemistry, 9, 2020, 1889-1900 (Impact factor: 3.116) [Link]
Chitrala Teja, Fazlur-Rahman Nawaz Khan, Asian Journal of Organic Chemistry, 9, 2020, 1889-1900 (Impact factor: 3.116) [Link]
191. Ir(I) Catalyzed Sequential Dehydrogenative Friedlander annulation-sp3 C-H activation towards (E)-4-benzylidenylacridin-1(2H)-ones, (E)-2-styryl quinoline-3-carboxamides"
191. Ir(I) Catalyzed Sequential Dehydrogenative Friedlander annulation-sp3 C-H activation towards (E)-4-benzylidenylacridin-1(2H)-ones, (E)-2-styryl quinoline-3-carboxamides"
Soda Prameela, Fazlur-Rahman Nawaz Khan* European Journal of Organic Chemistry, 2020, 2020 (33), 5394-5410, (Impact factor: 3.261) [Link]
Soda Prameela, Fazlur-Rahman Nawaz Khan* European Journal of Organic Chemistry, 2020, 2020 (33), 5394-5410, (Impact factor: 3.261) [Link]
190. Ru- catalyzed sequential dehydrogenative Friedlander reaction/Csp3-H activation/Knovenagel condensation in the regioselective synthesis of Chimanine B analogues
190. Ru- catalyzed sequential dehydrogenative Friedlander reaction/Csp3-H activation/Knovenagel condensation in the regioselective synthesis of Chimanine B analogues
Soda Prameela, Fazlur-Rahman Nawaz Khan* European Journal of Organic Chemistry, 2020, (19) 2888-2903 (Impact factor: 3.261) [Link]
Soda Prameela, Fazlur-Rahman Nawaz Khan* European Journal of Organic Chemistry, 2020, (19) 2888-2903 (Impact factor: 3.261) [Link]
189 Facile synthesis of 2-acylthieno[2,3-b]quinolines via Cu-TEMPO catalyzed dehydrogenation, sp2-C-H functionalization (Nucleophilic-thiolation by S8) of 2-haloquinolinyl ketones
189 Facile synthesis of 2-acylthieno[2,3-b]quinolines via Cu-TEMPO catalyzed dehydrogenation, sp2-C-H functionalization (Nucleophilic-thiolation by S8) of 2-haloquinolinyl ketones
Chitrala Teja and F Nawaz Khan, Organic Letters, 2020, 22, 5, 1726-1730 (Impact factor: 6.072 [Link]
Chitrala Teja and F Nawaz Khan, Organic Letters, 2020, 22, 5, 1726-1730 (Impact factor: 6.072 [Link]
188. Design, synthesis and biological evaluation of novel 9-methylbenzo (2, 3) (1, 4) oxazepino (7, 6-b) quinolines as potential antidiabetic agents
188. Design, synthesis and biological evaluation of novel 9-methylbenzo (2, 3) (1, 4) oxazepino (7, 6-b) quinolines as potential antidiabetic agents
P. Thiyagamurthy, Ramesh Dalavai , Gomathi Kannayiram , Naresh, Chirala Teja, Fazlur-Rahman Nawaz Khan*, Medicinal Chemistry Research 2020, 29, 1882–1901 (Impact factor: 2.351) [Link]
P. Thiyagamurthy, Ramesh Dalavai , Gomathi Kannayiram , Naresh, Chirala Teja, Fazlur-Rahman Nawaz Khan*, Medicinal Chemistry Research 2020, 29, 1882–1901 (Impact factor: 2.351) [Link]
187. Cu/TEMPO catalyzed dehydrogenation followed by 1,3-dipolar cycloaddition and their biological evaluation as potential antidiabetic agents
187. Cu/TEMPO catalyzed dehydrogenation followed by 1,3-dipolar cycloaddition and their biological evaluation as potential antidiabetic agents
Chitrala Teja, Spoorthy N Babu, Ayesha Noor, J. Arul Daniel, S. Asha Devi, and Fazlur Rahman Nawaz Khan*, RSC Advances 2020, 10, 12262-12271 (Impact factor: 4.036) [Link]
Chitrala Teja, Spoorthy N Babu, Ayesha Noor, J. Arul Daniel, S. Asha Devi, and Fazlur Rahman Nawaz Khan*, RSC Advances 2020, 10, 12262-12271 (Impact factor: 4.036) [Link]
186. A Base free Pd-Precatalyst Mediated Suzuki-Miyaura and Sonogashira cross-couplings in Deep Eutectic Solvents
186. A Base free Pd-Precatalyst Mediated Suzuki-Miyaura and Sonogashira cross-couplings in Deep Eutectic Solvents
P. Thiyagamurthy, FR. Nawaz Khan, Chemistry Select, 2020, 5, 2610-2617 (Impact factor: 2.307) [Link]
P. Thiyagamurthy, FR. Nawaz Khan, Chemistry Select, 2020, 5, 2610-2617 (Impact factor: 2.307) [Link]
185. Tetrabutylammonium-bromide promoted one-pot domino synthesis of spirooxindoles from alkyne-aldehyde coupling and 1,3-dipolar cycloaddition of azomethine ylides utilizing ytterbium triflate catalyst.
185. Tetrabutylammonium-bromide promoted one-pot domino synthesis of spirooxindoles from alkyne-aldehyde coupling and 1,3-dipolar cycloaddition of azomethine ylides utilizing ytterbium triflate catalyst.
Chitrala Teja and F Nawaz Khan, ChemistrySelect , 2020 5(21) 6470-6474, (Impact factor:2.307) [Link]
Chitrala Teja and F Nawaz Khan, ChemistrySelect , 2020 5(21) 6470-6474, (Impact factor:2.307) [Link]
184. RUCY-XylBINAP catalyzed and autoclave assisted rapid enantioselective synthesis of benzhydrols
184. RUCY-XylBINAP catalyzed and autoclave assisted rapid enantioselective synthesis of benzhydrols
183. In water: Green chemical approach of 4-iodo-3-(trimethylsilyl)-1H-pyrano[4,3-b]quinolines through 1,3-diiodo-5,5-dimethylhydantoin (DIH) mediated regioselective electrophilic
183. In water: Green chemical approach of 4-iodo-3-(trimethylsilyl)-1H-pyrano[4,3-b]quinolines through 1,3-diiodo-5,5-dimethylhydantoin (DIH) mediated regioselective electrophilic
