Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Shrikant M. Ghodse"'
Publikováno v:
Journal of Heterocyclic Chemistry. 59:800-803
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c61b7c9e414aa5c59c901d531e3d7363
https://doi.org/10.1002/jhet.4412
https://doi.org/10.1002/jhet.4412
Autor:
Shrikant M. Ghodse, Navnath T. Hatvate
Publikováno v:
Synthetic Communications. 50:3676-3683
A mild and convenient route for the synthesis of isoxazole derivatives has been developed using ZSM-5 as a heterogeneous catalyst. The reaction was carried out under a solvent-free condition to aff...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37b23bdbc3538c87f8c4f3c52cb02947
https://doi.org/10.1080/00397911.2020.1815786
https://doi.org/10.1080/00397911.2020.1815786
Publikováno v:
Letters in Organic Chemistry. 17:613-617
Metal-free synthesis of pyrimidinone (alky/aryl) via Biginelli reaction in the presence of aqueous sodium dichloroiodate (NaICl2) was studied under reflux conditions. Herein, we first time report the synthesis of the aliphatic Biginelli product by us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e88cd628ba2f46bfcfe21abae0b82ead
https://doi.org/10.2174/1570178617666191126095808
https://doi.org/10.2174/1570178617666191126095808
Autor:
Shrikant M. Ghodse, Pallavi Barde
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38d5ed3564d65b9286b500e1ec8228d8
https://doi.org/10.2139/ssrn.4215102
https://doi.org/10.2139/ssrn.4215102
Publikováno v:
Synthetic Communications. 49:3553-3559
In this paper, we report one-pot three-component synthesis of 5-substituted-1H-tetrazoles from aldehyde using zeolite-based heterogeneous catalyst (ZSM-5). Wide functional group tolerance with high chemical yield has been achieved. Moreover, heteroge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2c1f69e41ae30c9ac007df25f29e8a8
https://doi.org/10.1080/00397911.2019.1679185
https://doi.org/10.1080/00397911.2019.1679185
Publikováno v:
ChemistrySelect. 3:4168-4172
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f8967b5f8ddfc5079604c4104251a94
https://doi.org/10.1002/slct.201800690
https://doi.org/10.1002/slct.201800690
Publikováno v:
Tetrahedron Letters. 59:3892-3894
While continuing our research on Hunsdiecker reaction, we came across an interesting application of bleach, sodium hypochlorite (NaOCl) for decarboxylative chlorination reaction. The reaction is easily scaled up to 10 mmol. The reaction has good tole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38b902389f15513685afab4bf156c859
https://doi.org/10.1016/j.tetlet.2018.09.034
https://doi.org/10.1016/j.tetlet.2018.09.034
An efficient one-pot synthesis of 2-amino-1,3,4-thiadiazoles from easily available aldehydes and thiosemicarbazide using TBHP as an oxidant has been described. Notably, these reactions were carried out at room temperature using ethanol as solvent. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a149c257bc9f2e11b3778283d880c6a2
Publikováno v:
Journal of Chemical Sciences. 130
An efficient aqueous sodium dichloroiodate ( $$\hbox {NaICl}_{2})$$ mediated protocol is developed for the synthesis of benzofused azoles by the cyclization of 2-amino anilines/thiophenols/phenols with $$\beta $$ -diketone compounds. The reactions ga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9fe75f7cf48b6df7826cb5df9b2ba11
https://doi.org/10.1007/s12039-017-1414-z
https://doi.org/10.1007/s12039-017-1414-z
Autor:
Krishna N. Mundlod, Navnath T. Hatvate, Ghanshyam B. Jadhav, Shrikant M. Ghodse, Vikas N. Telvekar
Publikováno v:
Research Journal of Pharmacy and Technology. 13:4529
A novel series of 3-(4,5-dihydro-1H-pyrazol-3-yl)-4-hydroxy-2H-chromen-2-one derivatives was designed based on molecular hybridization technique. A series of 3-(1-benzoyl-5-phenyl-4,5-dihydro-1H-pyrazol-3-yl)-4-hydroxy-2H-chromen-2-one derivatives (6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59194a70925cd4b01752daeb7bf1911b
https://doi.org/10.5958/0974-360x.2020.00798.2
https://doi.org/10.5958/0974-360x.2020.00798.2