نتایج جستجو برای: utylbenzofuran pyrazoles synthesis

تعداد نتایج: 409489  

Journal: :International Journal of Molecular Sciences 2020

Journal: :Angewandte Chemie 2022

The α-arylation of cyclic and fluoroalkyl 1,3-diketones is made challenging by the highly stabilized nature corresponding enolates, especially difficult for sterically demanding aryl partners. As a general solution to this problem, we report Bi-mediated oxidative coupling acidic diones ortho-substituted arylboronic acids. Starting from bench-stable bismacycle precursor, sequence B-to-Bi transme...

Journal: :iranian journal of catalysis 0
rameshwar r. magar department of chemistry, dr. babasaheb ambedkar marathwada university, aurangabad (m.s.), 431004, india. ganesh t. pawar department of chemistry, dr. babasaheb ambedkar marathwada university, aurangabad (m.s.), 431004, india. sachin p. gadekar department of chemistry, dr. babasaheb ambedkar marathwada university, aurangabad (m.s.), 431004, india. machhindra k. lande department of chemistry, dr. babasaheb ambedkar marathwada university, aurangabad (m.s.), 431004, india.

the fe-mcm-22 zeolite was found to be an efficient solid heterogeneous catalyst for synthesis of dihydropyrano [2,3-c] pyrazoles via one pot four component reaction of ethyl acetoacetate, hydrazine hydrate, aromatic aldehyde and malononitrile in aqueous alcohol. the catalyst was synthesized by hydrothermal method under autogenous pressure and modified by fe (iii) ion exchange. the prepared cata...

2014
Konstantinos M. Kasiotis Evangelia N. Tzanetou Serkos A. Haroutounian

Angiogenesis is a mulit-step process by which new blood vessels are formed from preexisting vasculature. It is a key rate limiting factor in tumor growth since new blood vessels are necessary to increase tumor size. In this context it has been shown that anti-angiogenic factors can be used in cancer therapy. Among the plethora of heterocyclic compounds administered as anti-angiogenesis agents, ...

Journal: :Chemical communications 2016
Pradeep Sadhu Tharmalingam Punniyamurthy

A copper(II)-mediated regioselective N-arylation of azoles has been developed using 8-aminoquinoline amide as a directing group. This reaction shows a broad substrate scope with different azoles such as pyrroles, indoles, pyrazoles and carbazole with good yields.

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