Search Results - "Gaware, Sujeet"

Theophylline Hydrogen Sulfate: A green and efficient catalyst for synthesis of 3,3-bis(1H-indol-3-yl)indolin-2-one derivatives by Pund, Ganesh B., Wahul, Diksha B., Deshmukh, Tejshri R., Dhumal, Sambhaji T., Mandave, Krishna R., Gaware, Sujeet A., Farooqui, Mazahar, Dobhal, Bhagwansing S., Hebade, Madhav J.

“…A new green protocol for the synthesis of 3,3-bis(1H-indol-3-yl)indolin-2-one derivatives by reacting isatin with indole in the presence of Theophylline…”
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Meglumine Sulfate: An Efficient Catalyst for the Synthesis of Quinoxalines by Wahul, Diksha B., Pund, Ganesh B., Deshmukh, Tejshri R., Gaware, Sujeet A., Mandave, Krishna R., Hebade, Madhav J., Dhumal, Sambhaji T.

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Metal-free one-pot synthesis of 2-substituted benzimidazoles from N-aryl imines and TMSN3 by Gaware, Sujeet, Chatterjee, Rana, Dhayalan, Vasudevan, Dandela, Rambabu

“…[Display omitted] Iodine-catalysed efficient synthesis of 2-substituted benzimidazoles has been developed under aerobic condition. The one-pot oxidative…”
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Efficient Cross‐Dehydrogenative Coupling (CDC) Enabled by Cu‐PMo12 towards the Synthesis of Pyrimidinyl Carbamates at Room Temperature by Gaware, Sujeet, Chatterjee, Rana, Kotkondawar, Abhay Vijay, Dandela, Rambabu

“…A novel and efficient approach has been developed for the direct synthesis of pyrimidinyl dimethylcarbamate using Cu‐PMo12 complex. Basically, Cu‐PMA catalyst…”
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Efficient Cross‐Dehydrogenative Coupling (CDC) Enabled by Cu‐PMo 12 towards the Synthesis of Pyrimidinyl Carbamates at Room Temperature by Gaware, Sujeet, Chatterjee, Rana, Kotkondawar, Abhay Vijay, Dandela, Rambabu

“…Abstract A novel and efficient approach has been developed for the direct synthesis of pyrimidinyl dimethylcarbamate using Cu‐PMo 12 complex. Basically, Cu‐PMA…”
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An alternative synthetic strategy to construct apixaban analogues by Gaikwad, Dattatray, Chatterjee, Rana, Gaware, Sujeet, Acharya, Achyuta Nanda, Dandela, Rambabu

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Quadrol-Pd(II) complexes: phosphine-free precatalysts for the room-temperature Suzuki-Miyaura synthesis of nucleoside analogues in aqueous media by Serrano, José Luis, Gaware, Sujeet, Pérez, Jose Antonio, Pérez, José, Lozano, Pedro, Kori, Santosh, Dandela, Rambabu, Sanghvi, Yogesh S, Kapdi, Anant R

“…Commercially available Quadrol, , , ', '-tetrakis(2-hydroxypropyl)ethylenediamine (THPEN), has been used for the first time as a N^N-donor neutral hydrophilic…”
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Iodine‐Promoted Cascade Redox Cyclization to Access 2‐Arylbenzothiazoles Using Elemental Sulfur by Chiranjeevi, Yakkanti, Gaware, Sujeet, Chatterjee, Rana, Solanke, Jayshree, Venkateshwarlu, Rapolu, Rao, L. Vaikunta, Simhachalam, Gorle, Dandela, Rambabu

“…ABSTRACT A straightforward and efficient method has been developed to access a variety of benzothiazole derivatives via cascade reductive annulation. Iodine…”
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Silver molybdate (Ag‐PMo12) nanocomposite: An efficient catalyst for the one‐pot synthesis of 3,3‐diindolyl derivatives in aqueous medium by Gaware, Sujeet, Kamble, Omkar, Chatterjee, Rana, Kotkondawar, Abhay Vijay, Dandela, Rambabu

“…An efficient methodology has been developed for the synthesis of 3,3‐di(indolyl)oxindoles and bis(indolyl)methanes under mild conditions. The efficient…”
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Rapid plugged flow synthesis of nucleoside analogues via Suzuki-Miyaura coupling and heck Alkenylation of 5-Iodo-2’-deoxyuridine (or cytidine) by Gaware, Sujeet, Kori, Santosh, Serrano, Jose Luis, Dandela, Rambabu, Hilton, Stephen, Sanghvi, Yogesh S., Kapdi, Anant R.

“…Nucleosides modification via conventional cross-coupling has been performed using different catalytic systems and found to take place via long reaction times…”
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Greener Synthetic Approach for 4,4′‐(Arylmethylene)bis(3‐methyl‐1H‐pyrazol‐5‐ol) Derivatives in an Aqueous Medium using Theophylline as a Catalyst by Pund, Ganesh B., Dhumal, Sambhaji T., Deshmukh, Tejshri R., Wahul, Diksha B., Mandave, Krishna R., Gaware, Sujeet A., Chavan, Santosh S., Farooqui, Mazahar, Dobhal, Bhagwansing S., Hebade, Madhav J.

“…Herein, we report an efficient, convenient and environmentally benign method for the synthesis of 4,4′‐(arylmethylene)bis(3‐methyl‐1H‐pyrazol‐5‐ol)…”
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