Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Rathod Aravind Kumar"'
Autor:
Kashanna Jajula, Rathod Aravind Kumar, Ravada Kishore, Prakash Raj Thommandru, Ravula Shrikanth, Sirasani Satyanarayana, Pilli V. V. N. Kishore
Publikováno v:
New Journal of Chemistry. 46:2662-2668
The silver(i)-catalyzed dehydrogenative cross-coupling reaction of 2-aroylbenzofurans with phosphites to afford 2-aroyl-3-phosphonylbenzofurans is reported.
Autor:
Vijaya Babu Kummari, Rathod Aravind Kumar, Kalavakuntla Chiranjeevi, Alleni Suman Kumar, Jhillu S. Yadav
Publikováno v:
Synthetic Communications. 49:3335-3342
An efficient method for the synthesis of benzoxazoles and benzothiazoles via montmorillonite KSF clay catalyzed condensation reaction between 2-aminophenols or 2-aminothiophenols and β-diketones is reported. The efficiency of the reaction reflects f
Publikováno v:
RSC Advances. 9:31162-31168
The palladium(II)-catalyzed carbocyclization of benzenecarbaldehydes with internal alkynes to afford 2,3-disubstituted indenones was reported. The annulation reaction proceeded through the transmetalation of Pd(II) with an aromatic aldehyde and the i
Publikováno v:
ChemistrySelect. 3:8019-8022
Autor:
Nandkumar Doijad., Sowjanya Thatikonda, Chandraiah Godugu, Rathod Aravind Kumar, Nandan Kumar Duddukuri
Publikováno v:
ChemistrySelect. 3:6859-6864
Autor:
Jajula Kashanna, Duddukuri Nandan Kumar, Ravada Kishore, Rathod Aravind Kumar, Alleni Suman Kumar
Publikováno v:
Chemistrybiodiversity. 15(11)
Novel 2,3-dihydrofuran derivatives were synthesized through a tandem Knoevenagel-Michael cyclization in good yield by reacting α-tosyloxy ketone, 5,5-dimethyl-1,3-cyclohexanedione, and various aldehydes in the presence of phthalazine in acetonitrile
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
World Journal of Applied Chemistry. 4:14
The formation of amides from carboxylic acids and amines has been catalyzed efficiently with sodium hydrogen sulfate adsorbed on silica gel (NaHSO4.SiO2) at room temperature to give the products in high yields. The conversion carried out under reflux
Publikováno v:
European Journal of Chemistry. 4:191-194
A simple stereoselective synthesis of (+)-[6]-gingerdiol has been accomplished starting from vanillin. The synthetic sequence involves Mouroka allylation, diasterioselective iodine induced electrophilic cyclization and ring-opening of an epoxide as t
Publikováno v:
Tetrahedron Letters. 54:1634-1637
The conjugate addition on a natural bioactive pseudoguaianolide sesquiterpene lactone parthenin with various Grignard reagents leads to 13-C alkylated products chemo and diastereoselectively in fair overall yields. Compared with other Grignard reagen