Design and synthesis of novel thiazolidinone hybrid as α-amylase inhibitor, glucose uptake and antioxidant activity

Autor: Rameshwar M. More, Ashwini L. Jakkawad, Archana B. Kadam, Harish B. Musale, Vivek T. Humne, Subhash B. Junne

Publikováno v: Results in Chemistry, Vol 9, Iss , Pp 101657- (2024)

A design and synthesis of novel series of substituted thiazolidinone has been synthesised from 2-amino-thiazole and pyrazole-2-aldehyde using DCC under mild condition. These compounds were first examined for α-amylase inhibition, glucose uptake acti

Externí odkaz: https://doaj.org/article/e57ae60b429e4727ad0ca60d74501dc9

List of contributors

Autor: Charles Oluwaseun Adetunji, Sarfraz Ahmad, null Aiyshwaryalakshmi, O.O. Ajani, Romana Akhtar, Farah F. Al-Mamoori, G.D. Ametefe, M.K. Anusree, M.A. Aparna, Amit K. Bajhaiya, Asmita N. Bambole, Sagar Barale, Dinesh Chaudhari, Yogita Chavan, S.N. Chinedu, Sharda Choudhary, Elaine Da Costa, Mudasir Ahmad Dar, Pooja Doshi, Tahira Fardos, Rajesh Gacche, Sunil Gairola, Manish Gautam, Umesh B. Gawas, Sehrish Gazal, Sanjeev C. Ghadi, Savita Girawale, Ashok P. Giri, D.K. Gothwal, Puja Gupta, Vivek T. Humne, Khalid Hussain, Md Imran, E.E.J. Iweala, Swapnil Jadhav, Devika R. Jadhav, Shreeram Suresh Joglekar, Rakesh S. Joshi, Anup Atul Kale, Swapnil C. Kamble, Deepak M. Kasote, Lina Khandare, Priyanka Khot, Kisan M. Kodam, Hetika Kotecha, Gayatri D. Kotkar, Mohan Kulkarni, Brijesh Kumar, Naresh Kumar, Varsha Kumari, Poonam Kumari, Priyanka Kumawat, Navanath M. Kumbhar, Jisun H.J. Lee, Mahendra N. Lokhande, Mithil Mahale, Mahesh S. Majik, K. Manasa Leela, Surya Nandan Meena, Sharada D. Mohite, Vinod S. Nandre, Snehal K. Nimal, Osemwegie Osarenkhoe Omorefosa, Monika Pandita, Jyoti Parihar, Sarita Parihar, Sonia Parsekar, Yogita P. Patil, Dadasaheb Patil, Preethi Poduval, Madhu Raina, Subhisha Raj, Shyam Singh Rajput, Gulzar A. Rather, Nitin Rode, Beenish Sadaqat, Akshyakumar Sahoo, Sakshi Saini, Ramesh Saini, Joyita Sarkar, Rajashri Satvekar, Mohd Shahnawaz, Radheshyam Sharma, Abhijit D. Shetgaonkar, Pallavi Shewale, Bharat Shinde, Heena Shoket, Bhuri Singh, Mohd Yaseen Sirwal, Yogini Soman, Harshada Sowani, M. Sreehari, Arathi Sreenikethanam, Jianzhong Sun, Aafaq Tantray, Santosh Terdale, Amanpreet Thakur, Santosh G. Tilve, Chirag Varshney, Rongrong Xie, S.B. Yeri, Vasudeo Zambare, Daochen Zhu, Smita Zinjarde

Publikováno v: New Horizons in Natural Compound Research ISBN: 9780443152320

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::aa069d864e0cd86f0246cdd55e3e599c
https://doi.org/10.1016/b978-0-443-15232-0.01002-x

Copper-mediated rapid and facile oxidative dehydrogenation of dihydrobenzocarbazoles

Autor: Vivek T. Humne, Avinash G. Ulhe

Publikováno v: Synthetic Communications. 50:1064-1074

Rapid method for the oxidative dehydrogenation of dihydrobenzocarbazoles has been introduced by using bench scale and commercially available reagent; copper chloride, in excellent yield with easy workup. The scope of the reaction has been studied wit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bafd8c4e9090f0bc558e143778f94cd
https://doi.org/10.1080/00397911.2020.1731757

A one-pot direct regioselective iodination of Fischer-Borsche product using periodic acid in PEG-400

Autor: Vivek T. Humne, Monica H. Ghom, Mahavir S. Naykode, Pradeep D. Lokhande

Publikováno v: Tetrahedron Letters. 60:1029-1031

A metal-free and greener approach for the one-pot direct iodination and dehydrogenation of dihydrobenzo[a]carbazoles has been developed using periodic acid in polyethylene glycol-400 (PEG-400) under mild condition. This method has been proven to be t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7d859b200cf30e622d0b83f008de7e4a
https://doi.org/10.1016/j.tetlet.2019.03.022

Total synthesis of diverse oxygenated carbazoles by modified aromatization using molecular iodine

Autor: Monica H. Ghom, Mahavir S. Naykode, Vivek T. Humne, Pradeep D. Lokhande

Publikováno v: Tetrahedron Letters. 57:688-691

A convenient route has been developed for mono and dioxygenated carbazole alkaloids from 1-oxotetrahydrocarbazoles. The key step of the synthetic route is the aromatic process of 1-oxotetrahydrocarbazoles using molecular iodine. To our knowledge, thi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::690b6f97ed7f4515f85c675cbe5a7ea6
https://doi.org/10.1016/j.tetlet.2016.01.002