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- Sequential multicomponent catalytic synthesis of pyrrole-3-carboxaldehydes: evaluation of antibacterial and antifungal activities along with docking studies. Nisar A. Mir, Panduga Ramaraju, Satheeshvarma Vanaparthi, Sachin Choudhary, Rajnish P. Singh, Preetika Sharma, Rajni Kant, Rajpal Singh, Murugesan Sankaranarayanan, Indresh Kumar
, New J. Chem.
, 2020
, 44
, 16329
- One-pot sequential multicomponent reaction between in situ generated aldimines and succinaldehyde: facile synthesis of substituted pyrrole-3-carbaldehydes and applications towards medicinally important fused heterocycles. Anoop Singh, Nisar A. Mir, Sachin Choudhary, Deepika Singh, Preetika Sharma, Rajni Kant, Indresh Kumar
, RSC Adv.
, 2018
, 8
, 15448
- Sequential multicomponent site-selective synthesis of 4-iodo and 5-iodopyrrole-3-carboxaldehydes from a common set of starting materials by tuning the conditions. Sachin Choudhary, Jyothi Yadav, Mamta, Amol Prakash Pawar, Satheeshvarma Vanaparthi, Nisar A. Mir, Eldhose Iype, Ratika Sharma, Rajni Kant, Indresh Kumar
, Org. Biomol. Chem.
, 2020
, 18
, 1155
- Two-pot synthesis and photophysical studies of 1,6-disubstituted 5-aza-indoles from succinaldehyde and N-aryl propargylic-imines. Satheeshvarma Vanaparthi, Mamta, Jyothi Yadav, Amol Prakash Pawar, Eldhose Iype, Sravendra Rana, Indresh Kumar
, Org. Biomol. Chem.
, 2021
, 19
, 10601
- Two-pot sequential multicomponent metal-free synthesis of pyrrolo[2,3-d]pyridazin-7-ones and pyrrolo[2,3-d]pyrizidines. Mamta, Nisar A. Mir, Jyothi Yadav, Amol Prakash Pawar, Ratika Sharma, Rajni Kant, Krishnan Rangan, Eldhose Iype, Bharti Khungar, Indresh Kumar
, New J. Chem.
, 2023
, 47
, 14637
- Microwave assisted aminocatalyzed [3 + 2] annulation between α-iminonitriles and succinaldehyde: synthesis of pyrrole-3-methanols and related polycyclic ring systems. Nisar A. Mir, Sachin Choudhary, Panduga Ramaraju, Deepika Singh, Indresh Kumar
, RSC Adv.
, 2016
, 6
, 39741
- A carbon nitride supported copper nanoparticle composite: a heterogeneous catalyst for the N-arylation of hetero-aromatic compounds. Debkumar Nandi, Samarjeet Siwal, Kaushik Mallick
, New J. Chem.
, 2017
, 41
, 3082
- Selective synthesis of pyrrolidin-2-ones and 3-iodopyrroles via the ring contraction and deformylative functionalization of piperidine derivatives. Fang Wang, Xinying Zhang, Yan He, Xuesen Fan
, Org. Biomol. Chem.
, 2019
, 17
, 156
- N-(1-Oxy-2-picolyl)oxalamic acids as a new type of O,O-ligands for the Cu-catalyzed N-arylation of azoles with aryl halides in water or organic solvent. Yongbin Wang, Yu Zhang, Beibei Yang, Ao Zhang, Qizheng Yao
, Org. Biomol. Chem.
, 2015
, 13
, 4101
- Pyrrole: a resourceful small molecule in key medicinal hetero-aromatics. Varun Bhardwaj, Divya Gumber, Vikrant Abbot, Saurabh Dhiman, Poonam Sharma
, RSC Adv.
, 2015
, 5
, 15233