Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Baliram S. Hote"'
Autor:
Gajrali M. Patel, Abhijeet S. Kure, Gajanan G. Mandawad, Baliram S. Hote, Shankaraiah G. Konda
Publikováno v:
Results in Chemistry, Vol 4, Iss , Pp 100436- (2022)
In this present communication, one-pot synthesis of bis(indolyl)methane derivatives (3a-t) achieved from the condensation of indole (1) with various substituted benzaldehydes (2a-t) using [DSIM][AlCl3]x-@CS chitosan supported ionic liquid (CSIL) as c
Externí odkaz:
https://doaj.org/article/b8c00aba3716404196891aa963cd551b
Publikováno v:
E-Journal of Chemistry, Vol 8, Iss 3, Pp 1339-1345 (2011)
An improved and rapid one pot synthesis of 2,4,6-triphenyl-1H-imidazoles on condensation with benzil, aromatic aldehyde and NH4OAc has been carried out using ZnO as an efficient and inexpensive catalyst in high yield at room temperature. The short re
Externí odkaz:
https://doaj.org/article/8a2ff0de31cb4a3cb5e60631c1799684
Autor:
Abhijeet S. Kure, Shankaraiah G. Konda, Santosh S. Chobe, Gajanan G. Mandawad, Baliram S. Hote
In this present communication, four component, one pot synthesis of benzyl pyrazolyl coumarin (5a-m) derivatives achieved from the condensation of phenyl hydrazine (1), ethyl acetoacetate (EAA, 2), various substituted benzaldehyde (3), and 4-hydroxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8ff93ac2a40ec069b9fce2288285d49
Autor:
Gajanan G. Mandawad, Shankaraiah G. Konda, Santosh S. Chobe, Amit Kumar N. Gosar, Baliram S. Hote
Publikováno v:
Current organic synthesis. 19(6)
Aim: The aim of this present work was to design and establish an efficient synthesis of new thienyl pyrazolo[1,5‐a] pyrimidines using an environmentally friendly reaction solvent. Further, the newly synthesized compounds were evaluated for antimi-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f9be7e080d8aaea84897874fb6f8b04
https://pubmed.ncbi.nlm.nih.gov/35249494
https://pubmed.ncbi.nlm.nih.gov/35249494
A simple and efficient procedure for the synthesis of polyhydroquinolines (5a-l) was developed, involving one pot four component Hantzsch condensation of dimedone 1, various substituted benzaldehydes 2, ethyl acetoacetate (EAA) 3 and ammonium acetate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8654677ed22b18bc8ed3c4293f404f52
One of the synthetic intermediates is used in many organic transformations. We have developed highly efficient N-formylation of anilines (3a–l) under solvent- and catalyst free using 150 W tungsten lamp under visible light. High yields of products,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b3ea754a8e5abe68a2113a0e775221e
A mild and highly efficient stereoselective reaction using silica supported bismuth(III) chloride (SiO2-BiCl3) has been successfully employed in the synthesis of 6-methyl-2-aryl-4, 5-dihydropyridazin-3(2H)-one derivatives (3a-o) with a variety of phe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48c2540109299eca5cf6153ee84de533
An efficient procedure has been developed for the synthesis of bis(indolyl)methanes (3a-m) from condensation of indole (1) and various substituted aromatic aldehydes (2a-m) is described. The aromatic electrophilic substitution reactions of indole (1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e950a4889b61934fb42b5bf03232c3a6
Simple, mild and highly efficient protocol has been developed by using heterogeneous silica supported SiO2-BiCl3 (5 mol%) catalyst from the condensation of pyrrole (1, 2 mol%) and various substituted aryl aldehyde(2, 1 mol%) to afforded meso-dipyrrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44e41dd66fecae9ddad466485ad9fd32
An efficient and clean method was developed for the three components, one-pot synthesis of pyrimidinone/thione derivatives using cyclopentanone, variety of aromatic aldehydes, and urea/thiourea by using cyanuric chloride catalyzed Biginelli-type reac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f54a1cbc95ae0915bc85c9acb01fb83