Three Component Reaction: An Efficient Synthesis and Reactions of 3,4-Dihydropyrimidin-2(1H)-Ones and Thiones Using New Natural Catalyst

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Three Component Reaction: An Efficient Synthesis and Reactions of 3,4-Dihydropyrimidin-2(1H)-Ones and Thiones Using New Natural Catalyst

Synthesis of 3,4-dihydropyrimidin-2(1H)-one and 3,4-dihydropyrimidin-2(1H)-thione derivatives from aldehydes, 1,3-dicarbonyl derivatives and urea or thiourea using granite and quartz as new, natural and reusable catalysts. Some of the 3,4-dihydropyrimidin-2(1H)-thione derivatives were used to prepare new heterocyclic compounds. The antimicrobial activity of selected examples of the synthesized ...

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New method for preparation of MWCNT-SO3H as an efficient and reusable catalyst for the solvent-free synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones

Multiwalled carbon nanotubes (MWCNTs) have been functionalized with -SO3H groups using new three steps chemical routes. Firstly, OH groups have been attached to CNT surfaces through a radical reaction. The second step involves converting the hydroxyl groups into the oxide one and last step included the attachment of –SO3H groups on the MWCNTs surfaces in the presence of 1-butyl-3-methyl imidazo...

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New method for preparation of MWCNT-SO3H as an efficient and reusable catalyst for the solvent-free synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones

Multiwalled carbon nanotubes (MWCNTs) have been functionalized with -SO3H groups using new three steps chemical routes. Firstly, OH groups have been attached to CNT surfaces through a radical reaction. The second step involves converting the hydroxyl groups into the oxide one and last step included the attachment of –SO3H groups on the MWCNTs surfaces in the presence of 1-butyl-3-methyl imidazo...

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A rapid and convenient synthesis of 5-unsubstituted 3,4-dihydropyrimidin- 2-ones and thiones

A rapid and convenient synthesis of 5-unsubstituted 3,4-dihydropyrimidin-2-ones and thiones was developed. The reaction involves a one-pot reaction between oxalacetic acid, thiourea/urea, and aldehyde under microwave irradiation and provides the products in good yields and much shorter reaction times. 2010 Elsevier Ltd. All rights reserved.

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ژورنال

عنوان ژورنال: ISRN Organic Chemistry

سال: 2013

ISSN: 2090-5157

DOI: 10.1155/2013/706437