Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Nagi Reddy Modugu"'
Autor:
Goverdhan Mehta, Nagi Reddy Modugu
Publikováno v:
The Journal of Organic Chemistry. 83:10573-10579
A flexible synthesis of the carbocyclic core present in glycosides xylosmin and flacourtosides E and F, natural products exhibiting antimalarial and antiarboviral activities, has been accomplished. Our approach emanates from the Diels-Alder adduct of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::650e015d85a352b75e58788374405cd4
https://doi.org/10.1021/acs.joc.8b01389
https://doi.org/10.1021/acs.joc.8b01389
Publikováno v:
ChemistrySelect. 3:7766-7770
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96fd80a00bdfb334be1ff512f9da8199
https://doi.org/10.1002/slct.201801089
https://doi.org/10.1002/slct.201801089
Autor:
Praveen Kumar Pittala, Rajanarendar Eligeti, Y N Reddy, Nagi Reddy Modugu, Nagaraju Dharavath
Publikováno v:
ChemistrySelect. 2:5110-5114
Polyethylene glycol-400 (PEG-400) has been discovered as an efficient and eco-friendly reaction medium for the synthesis of new isoxazolyl indole-3-carboxylic acid esters 11 from 4-amino-3-methyl-5-styrylisoxazoles 7. Compounds 7 on treatment with β
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bc6611aa1ce34fe5f322941e569211a
https://doi.org/10.1002/slct.201700640
https://doi.org/10.1002/slct.201700640
Publikováno v:
ChemistrySelect. 2:2651-2654
1-Methyl imidazolium tetraflouroborate ([HMIm]BF4) has been discovered to be an effective eco-friendly solvent cum activator for a novel one-pot sequential coupling and oxidative cyclization of 4-amino-3-methyl-5-styrylisoxazoles, 2-aminobenzoyl chlo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d8b3e5d4450b238e6d06814dd27dc03
https://doi.org/10.1002/slct.201700247
https://doi.org/10.1002/slct.201700247
Publikováno v:
New Journal of Chemistry. 41:14062-14066
An efficient, inexpensive and environmentally friendly synthesis of novel isoxazole substituted spirooxindole-pyridopyrimidine/indenopyridine/chromenopyridine/naphthyridine/quinoline derivatives has been developed via one-pot three-component reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::433b7fe393e616a4fa4e798f287b7faf
https://doi.org/10.1039/c7nj03515b
https://doi.org/10.1039/c7nj03515b
Autor:
Goverdhan Mehta, Nagi Reddy Modugu
Publikováno v:
Tetrahedron Letters. 59:4036-4038
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80a150b1b4d51194db34b986a6236526
https://doi.org/10.1016/j.tetlet.2018.09.063
https://doi.org/10.1016/j.tetlet.2018.09.063
Publikováno v:
Tetrahedron Letters. 56:6919-6922
A synthetic approach towards kinamycins that harnesses the proclivities of the norbornyl scaffold is unveiled to access the oxy-functionalized and actively side-armed cyclohexenoid ring-D of these bioactive natural products. This ring-D building bloc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::321f7452d3a169142a0891253795d5ca
https://doi.org/10.1016/j.tetlet.2015.11.001
https://doi.org/10.1016/j.tetlet.2015.11.001
Publikováno v:
In Tetrahedron Letters 20 December 2017 58(51):4790-4795
Autor:
Goverdhan Mehta, Nagi Reddy Modugu
Publikováno v:
Tetrahedron Letters. 56:6030-6033
A new, short, approach toward bioactive antroquinonols has been conceptualized wherein the key carbocyclic core has been readily assembled employing disposable norbornyl scaffold as the regio- and stereo-director and a Wittig olefination based strate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcb12321de530162bb03f99fe17bc471
https://doi.org/10.1016/j.tetlet.2015.09.043
https://doi.org/10.1016/j.tetlet.2015.09.043
Publikováno v:
Cogent Chemistry, Vol 3, Iss 1 (2017)
We report a mild, inexpensive, fast, highly efficient, and eco-friendly protocol for the synthesis of new isoxazolyl dihydro-1H-indol-4(5H)-ones by a catalyst-free, one-pot three-component reaction of 4-amino-3-methyl-5-styrylisoxazoles, dimedone, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdd80bd5f3793743d655980bc032ca7d
https://doaj.org/article/6c5c85775a434137a0fb2b964835259a
https://doaj.org/article/6c5c85775a434137a0fb2b964835259a