Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ashok S. Pise"'
Publikováno v:
ChemistrySelect. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99eedcc2d1e7bcacf04576e3c06d43e7
https://doi.org/10.1002/slct.202201590
https://doi.org/10.1002/slct.202201590
Publikováno v:
International Journal of Scientific Research in Science and Technology. :06-12
The protecting group plays important role in synthesis of multifunctional targets. A simple rapid efficient and green method for chemo-selective N-Boc protection of amines using Lithium hydroxide as a green catalyst. In the present work amine protect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ec1adfbfde5b51a7c6ed8401b050d14
https://doi.org/10.32628/ijsrst20751
https://doi.org/10.32628/ijsrst20751
Publikováno v:
International Journal of Scientific Research in Science and Technology. :332-339
A simple, convenient, and environmentally friendly method for the synthesis of 1,3-oxazine derivatives has been developed under aqueous conditions. The reaction proceeds via one pot multicomponent condensation of ? or ?- naphthol, aromatic aniline an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f19734f3b9f23d2042e2112cc9e215ae
https://doi.org/10.32628/ijsrst207482
https://doi.org/10.32628/ijsrst207482
Publikováno v:
Asian Journal of Chemistry. 32:575-579
A new efficient and convenient approach towards the synthesis of pyrazole is described. The α,β-unsaturated cyanoesters were obtained from substituted benzaldehyde and ethyl cyanoacetate by reported methods. 1,5-Disubstituted pyrazoles were synthes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d2af41cd095085b5ed07bf975a3948a
https://doi.org/10.14233/ajchem.2020.22432
https://doi.org/10.14233/ajchem.2020.22432
Publikováno v:
Asian Journal of Organic & Medicinal Chemistry. 5:36-39
The β-amino compounds were synthesized from α,β-unsaturated esters, nitriles and amine using water as a solvent in the presence of 10 mol % Cu(I) catalyst in high yields within 2-5 min under ultrasound irradiation at room temperature. The reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::065a6fa6b04f3676d6c00b5f8b1f34e8
https://doi.org/10.14233/ajomc.2020.ajomc-p232
https://doi.org/10.14233/ajomc.2020.ajomc-p232
Publikováno v:
Asian Journal of Chemistry. 31:2841-2845
The epoxides were obtained from substituted phenols and epichlorohydrin by reported methods. The regioselective ring opening of epoxides were studied in different solvents by reaction with Grignard’s reagent in presence of dilithium tetrachloromang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c156713f1458add864d46f7db76fa5e6
https://doi.org/10.14233/ajchem.2019.22270
https://doi.org/10.14233/ajchem.2019.22270
Publikováno v:
Asian Journal of Organic & Medicinal Chemistry. 4:194-199
The regioselective epoxide ring opening at less substituted carbon atom of epoxide were reported by nucleophiles like heterocyclic amines which gives well known 1,2-difunctionalized amino alcohols. These are present in many synthetic as well as natur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d95262b0a28e8afdb4a2b2fb63310aba
https://doi.org/10.14233/ajomc.2019.ajomc-p213
https://doi.org/10.14233/ajomc.2019.ajomc-p213
Sulfated tungstate catalyzed an efficient and ecofriendly protocol has been described for the synthesis of 2-substituted benzothiazoles. The corresponding benzothiazoles were obtained using a condensation reaction of 2-aminothiophenol with various al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c2567ee2837659d6d16d4bf66bf6241
Publikováno v:
Asian Journal of Chemistry. 31:348-352
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2a7eb4ed8ff1e7aa348595171bd96fe
https://doi.org/10.14233/ajchem.2019.21613
https://doi.org/10.14233/ajchem.2019.21613
Publikováno v:
Asian Journal of Chemistry. 30:894-896
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::350e5d649484f004fca48b3f36d2196e
https://doi.org/10.14233/ajchem.2018.21131
https://doi.org/10.14233/ajchem.2018.21131