Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tukaram D. Urmode"'
Autor:
Prashant A. Kulkarni, Mahendra A. More, Tukaram D. Urmode, Kisan M. Kodam, Navanath Kumbhar, Vinod S. Nandre, Rahul V. Khade
Publikováno v:
ACS Omega
ACS Omega, Vol 5, Iss 17, Pp 9668-9673 (2020)
ACS Omega, Vol 5, Iss 17, Pp 9668-9673 (2020)
In this study, a siderophore, pyoverdine (PVD), has been isolated from Pseudomonas sp. and used to develop a fluorescence quenching-based sensor for efficient detection of nitrotriazolone (NTO) in aqueous media, in contrast to other explosives such a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e30dbe3b1857db53f175d1c4a4e5fc6d
http://europepmc.org/articles/PMC7203702
http://europepmc.org/articles/PMC7203702
Autor:
Sajad Malik, Radhika S. Kusurkar, Saroj S. Ghaskadbi, Smriti P.K. Mittal, Tukaram D. Urmode, Swati Khole
Publikováno v:
Journal of Traditional and Complementary Medicine, Vol 9, Iss 1, Pp 38-44 (2019)
Livotrit®, a polyherbal formulation (Zandu, India) is commonly prescribed for liver health. The present study was undertaken to elucidate possible mechanism of antioxidant potential of Livotrit®. Livotrit® exhibited concentration dependent radical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce25b90eb4d3d203e28c8272e5c87871
https://doi.org/10.1016/j.jtcme.2017.08.007
https://doi.org/10.1016/j.jtcme.2017.08.007
Publikováno v:
Tetrahedron. 73:4348-4354
A recyclable catalyst, β-cyclodextrin-SO3H in aqueous medium was used effectively for the synthesis of spiroindolones (tetrahydrospiro-β-carbolines as well as tetrahydrospiro-γ-carbolines) in a Pictet-Spengler spirocyclisation. The products were o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbacfde97c6261da2d096feca73933b2
https://doi.org/10.1016/j.tet.2017.05.089
https://doi.org/10.1016/j.tet.2017.05.089
Publikováno v:
ChemistrySelect. 2:2552-2555
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3bb072434d1474a0a55fa291f2bb51b
https://doi.org/10.1002/slct.201700215
https://doi.org/10.1002/slct.201700215
Three differently substituted, naturally occurring, biologically active carbazole derivatives (viz. ekeberginine, murrayaquinone A, and glycozoline) were synthesized in good yield using short and simple routes. The prenyl group was selectively introd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::198f58328e3016f13ac1c561f17e7314
Three differently substituted naturally occurring, biologically active carbazole derivatives viz. ekeberginine, murrayaquinone A and glycozoline were synthesized in good yield using short and simple routes. Prenyl group was selectively introduced at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::738a346e7a2cfec1ba5b5a8045e9406c
Publikováno v:
ChemInform. 45
Two novel routes are elaborated for the synthesis of the naturally occurring alkaloid bouchardatine (I).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5c652a626069274a799792528f75375
https://doi.org/10.1002/chin.201408222
https://doi.org/10.1002/chin.201408222
Publikováno v:
Australian Journal of Chemistry. 66:1112
Two new, efficient and simple routes using Heck-type reaction and intramolecular cyclization were developed for the synthesis of the naturally occurring cytotoxic alkaloid 2-(4-oxo-3,4-dihydroquinazolin-2-yl)-1H-indole-3-carbaldehyde (bouchardatine).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb716d0ee6c33ab223dc302ca6d5ed7e
https://doi.org/10.1071/ch13331
https://doi.org/10.1071/ch13331
Autor:
Momin, Aadil A.1 (AUTHOR), Urmode, Tukaram D.1 (AUTHOR), Bhosale, Shrikar M.1 (AUTHOR), Kusurkar, Radhika S.1 (AUTHOR) rsk@chem.unipune.ac.in
Publikováno v:
Synthetic Communications. 2016, Vol. 46 Issue 15, p1292-1298. 7p. 6 Diagrams.
Autor:
Naik, Nilesh H.1,2, Urmode, Tukaram D.1, Sikder, Arun K.2, Kusurkar, Radhika S.1 rsk@chem.unipune.ac.in
Publikováno v:
Australian Journal of Chemistry. 2013, Vol. 66 Issue 9, p1112-1114. 7p.