An Easy and Efficient Protocol for the Synthesis of 2,3-Dihydroquinazolinones Using a Low Cost and Reusable Heterogeneous Catalyst
نویسندگان
چکیده
منابع مشابه
nano-rods zno as an efficient catalyst for the synthesis of chromene phosphonates, direct amidation and formylation of amines
چکیده ندارد.
Clean, reusable and low cost heterogeneous catalyst for amide synthesis.
We have developed a heterogeneous silica catalyst that can effectively catalyse amide synthesis from acid and amine, without production of toxic by-products and with the advantage of being readily available, low cost, environmentally benign and reusable.
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Silica sulfuric acid as an efficient and reusable heterogeneous catalyst has been used for the preparation of amidines 2 from formimidate 1 by reaction with aromatic amines at room temperature in good to excellent yields. Imidate was prepared by treatment of equimolar quantities of triethyl orthoformate and diaminomaleonitrile in refluxing dioxane. All the compounds were characterized fully by ...
متن کاملSilica sulfuric acid as an efficient and reusable heterogeneous catalyst for the synthesis of formamidines from the diaminomaleonitrile
Silica sulfuric acid as an efficient and reusable heterogeneous catalyst has been used for the preparation of amidines 2 from formimidate 1 by reaction with aromatic amines at room temperature in good to excellent yields. Imidate was prepared by treatment of equimolar quantities of triethyl orthoformate and diaminomaleonitrile in refluxing dioxane. All the compounds were characterized fully by ...
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To prepare ultra-clean gasoline fuel, a new nanocomposite TBA-PV2Mo10@PVA was introduced as an efficient and green catalyst for oxidative desulfurization (ODS) process. The nanocomposite was successfully prepared by reaction of tetrabutylammonium bromide (TBA), H5PMo10V2O40, and poly vinyl alcohol (PVA) at room temperature via sol–gel method under oil-bath condition. The synthesized TBA-PV2Mo10...
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ژورنال
عنوان ژورنال: American Journal of Chemistry
سال: 2012
ISSN: 2165-8749
DOI: 10.5923/j.chemistry.20120205.02