Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Siddhartha, Maiti"'
Autor:
Farzana Naushin, Srishti Sen, Mukul Kumar, Hemang Bairagi, Siddhartha Maiti, Jaydeep Bhattacharya, Somaditya Sen
Publikováno v:
ACS Omega, Vol 9, Iss 1, Pp 464-473 (2023)
Externí odkaz:
https://doaj.org/article/80aad1a6dbe6460e8ac0c25cfc325bb1
Autor:
Manisha Poudyal, Komal Patel, Laxmikant Gadhe, Ajay Singh Sawner, Pradeep Kadu, Debalina Datta, Semanti Mukherjee, Soumik Ray, Ambuja Navalkar, Siddhartha Maiti, Debdeep Chatterjee, Jyoti Devi, Riya Bera, Nitisha Gahlot, Jennifer Joseph, Ranjith Padinhateeri, Samir K. Maji
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-21 (2023)
Abstract Liquid-liquid phase separation (LLPS) has emerged as a crucial biological phenomenon underlying the sequestration of macromolecules (such as proteins and nucleic acids) into membraneless organelles in cells. Unstructured and intrinsically di
Externí odkaz:
https://doaj.org/article/b30a93f83546417b873e83f6d8ce220c
Autor:
Ranjini Laskar, Tanay Pal, Trisha Bhattacharya, Siddhartha Maiti, Munetaka Akita, Debabrata Maiti
Publikováno v:
Green Chemistry. 24:2296-2320
This tutorial review gathers landmark work on transition-metal mediated C–H activation reactions using more sustainable approaches. We endeavour to promote and propagate such lines of research, reducing the usage of hazardous synthetic routes in ch
Publikováno v:
Chemical Society Reviews. 51:7358-7426
Transition metal catalysis has contributed immensely to C-C bond formation reactions over the last few decades, and alkylation is no exception. The superiority of such methodologies over traditional alkylation is evident from minimal reaction steps,
Autor:
Jaishri Chopra, Mohamed Mokhtar, Siddhartha Maiti, Tanay Pal, Debabrata Maiti, Prabhat Kumar Baroliya, Shaeel A. Al-Thabaiti
Publikováno v:
ChemCatChem. 13:4655-4678
Autor:
Nesreen S.I. Ahmed, Debabrata Maiti, Mohamed Mokhtar M. Mostafa, Siddhartha Maiti, Sandeep Pimparkar, Adithyaraj Koodan
Publikováno v:
Chemical Communications. 57:2210-2232
Nitrile or cyano compounds are an important part of structural motifs in dyes, agrochemicals, medicinal compounds, and electronic materials. Also, aryl nitrile is an important intermediate in the preparation of numerous compounds via transformations
Publikováno v:
Nutrition and Cancer. 73:2477-2490
Medicinal plants offer enormous possibilities in the quest of novel bioactive formulation for cancer therapy. Here, we studied the anticancer efficacy of the extract of edible tuber Amorphophallus paeoniifolius (Dennst.) (APTE) against estrogen posit
Autor:
Sandhya Bhatia, Amrendra K. Singh, Jaladhar Mahato, Soumik Ray, Ranjith Padinhateeri, Samir K. Maji, Laxmikant G. Gadhe, Siddhartha Maiti, Ambuja Navalkar, Roland Riek, Debdeep Chatterjee, Rajlaxmi Panigrahi, G. Krishnamoorthy, Nitu Singh, Sushil Kumar Pandey, Rakesh Kumar, Arindrajit Chowdhury, Komal Patel, Surabhi Mehra, Juan Gerez, Debalina Datta, Ashutosh Kumar
Publikováno v:
Nature Chemistry. 12:705-716
α-Synuclein (α-Syn) aggregation and amyloid formation is directly linked with Parkinson's disease pathogenesis. However, the early events involved in this process remain unclear. Here, using the in vitro reconstitution and cellular model, we show t
Autor:
Manisha Poudyal, Komal Patel, Ajay Singh Sawner, Laxmikant Gadhe, Pradeep Kadu, Debalina Datta, Semanti Mukherjee, Soumik Ray, Ambuja Navalkar, Siddhartha Maiti, Debdeep Chatterjee, Riya Bera, Nitisha Gahlot, Ranjith Padinhateeri, Samir K. Maji
Liquid-liquid phase separation (LLPS) has emerged as a crucial biological mechanism for sequestering macromolecules (such as proteins and nucleic acids) into membraneless organelles in cells. Unstructured and intrinsically disordered domains are know
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51abe59636e8b30d021cf54d27fa5012
https://doi.org/10.1101/2021.12.31.474648
https://doi.org/10.1101/2021.12.31.474648
Publikováno v:
Polyhedron. 172:120-124
Aromatic nitro compounds are extensively used in synthetic chemistry. We disclose a new approach to obtain nitroarenes regioselectively starting from carboxylic acids under acid-free reaction conditions.