@article { ISI:000362919100021,
	title = {Mild regiospecific alcoholysis and aminolysis of epoxides catalyzed by zirconium(IV) oxynitrate},
	journal = {Tetrahedron Letters},
	volume = {56},
	number = {43},
	year = {2015},
	month = {OCT},
	pages = {5916-5919},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A regiospecific method for the ring-opening reaction of epoxides by the primary, secondary, tertiary alcohols, and aryl, aliphatic amines has been developed using non-toxic metal nitrate salt as a catalyst. The best results were obtained using zirconium(IV) oxynitrate among the various screened metal nitrate salts. The reported protocol works efficiently for styrene epoxide and aliphatic as well. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Alcoholysis, Aminolysis, Epoxide, Lewis acid, Zirconia},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2015.09.031},
	author = {Shinde, Sandip S. and Said, Madhukar S. and Surwase, Trupti B. and Kumar, Pradeep}
}
@article {43054,
	title = {Molybdenum oxide-mediated facile aliphatic nucleophilic fluorination},
	journal = {Tetrahedron Letters},
	volume = {58},
	year = {2017},
	month = {NOV},
	pages = {59-62},
	type = {Article},
	doi = {10.1016/j.tetlet.2016.11.099},
	author = {Said, Madhukar S. and Khandare, Leena and Shinde, Sandip S.}
}
@article {47588,
	title = {Metal-free, Tf2NH-catalyzed 1, 6-conjugate addition of imidazopyridine to para-quinone methides: easy access to C3-functionalized triarylmethane imidazopyridine},
	journal = {Tetrahedron},
	volume = {101},
	year = {2021},
	month = {NOV},
	pages = {132510},
	type = {Article},
	abstract = {An inexpensive and commercially available Tf2NH-catalyzed 1,6-conjugate addition of imidazopyridine (IMPY) heterocycles to para-quinone methides (p-QMs) is reported. The present transformation provides a diverse class of C3-functionalized triarylmethanes heterocyclic derivatives of imidazopyridine. These metal-free transformations provided a very broad substrate scope of conjugate addition product with a high yield up to 97\% within a short duration. (C) 2021 Elsevier Ltd. All rights reserved.},
	keywords = {1, 6-Conjugate addition, Bronsted acid, C3-functionalization, Imidazopyridine, para-Quinone methide},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2021.132510},
	author = {Khonde, Nilesh S. and Said, Madhukar S. and Sabane, Jagjivan K. and Gajbhiye, Jayant M. and Kumar, Pradeep}
}
@article {50143,
	title = {Marine Arthrobacter enclensis NIO-1008T as a salicylic acid producing biocontrol agent against Fusarium oxysporum},
	journal = {European Journal of Plant Pathology},
	volume = {174},
	year = {2026},
	month = {JUN},
	pages = {1103-1120},
	type = {Article},
	abstract = {<p>
	The importance of microorganisms in plant growth promotion (PGP) and disease control has long been acknowledged. However, marine bacteria have been largely neglected in agricultural applications. In this study, previously identified marine strain Arthrobacter enclensis NIO-1008T has been explored for mitigation of Fusarium oxysporum NCIM 1281 infestation on wheat plants. A genome analysis study confirmed strain NIO-1008T has protein encoding genes associated with stress tolerance, antifungal activity and PGP. A growth attributes study showed strain NIO-1008T has the ability to grow at 4-11 pH, 6\% NaCl and in presence of heavy metals. PGP traits, such as ammonia, siderophore and total indole (640 +/- 9 mu g/mL), were also confirmed. Moreover, an antagonistic assay showed 66 +/- 2\% F. oxysporum mycelial growth inhibition. Furthermore, NMR data confirmed strain NIO-1008T produced salicylic acid (SA), which inhibited spore germination and mycelial growth. A greenhouse pot experiment showed that disease incidence significantly reduced to 70\% in the presence of strain NIO-1008T, and 45.7\% in SA, compared to control wheat plants. This study concludes A. enclensis NIO-1008T is a potential biocontrol candidate against F. oxysporum.</p>
},
	keywords = {<italic>F. oxysporum</italic>, Antifungal compound, Biocontrol activity, Marine bacteria, Salicylic acid},
	issn = {0929-1873},
	doi = {10.1007/s10658-026-03187-5},
	author = {Kharat, Bharat A. and Said, Madhukar S. and Dastager, Syed G.}
}
