Unknown

Dataset Information

0

An Efficient, Eco-friendly and Sustainable One-Pot Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones Directly from Alcohols Catalyzed by Heteropolyanion-Based Ionic Liquids.


ABSTRACT: Efficient, eco-friendly and sustainable access to 3,4-dihydropyrimidin-2(1H)-ones directly from alcohols under microwave and solvent-free conditions has been reported. The practical protocol involves heteropolyanion-based catalyzed oxidation of alcohols to aldehydes with NaNO? as the oxidant followed by cyclocondensation with dicarbonyl compounds and urea or thiourea in a two-step, one-pot manner. Compatibility with different functional groups, good to excellent yields and reusable catalysts are the main highlights. The utilization of alcohols instead of aldehydes is a valid and green alternative to the classical Biginelli reaction.

SUBMITTER: Fu R 

PROVIDER: S-EPMC6151647 | biostudies-literature | 2017 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications

An Efficient, Eco-friendly and Sustainable One-Pot Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones Directly from Alcohols Catalyzed by Heteropolyanion-Based Ionic Liquids.

Fu Renzhong R   Yang Yang Y   Ma Xudong X   Sun Yu Y   Li Jin J   Gao Hang H   Hu Huaxing H   Zeng Xiaojun X   Yi Jun J  

Molecules (Basel, Switzerland) 20170911 9


Efficient, eco-friendly and sustainable access to 3,4-dihydropyrimidin-2(1<i>H</i>)-ones directly from alcohols under microwave and solvent-free conditions has been reported. The practical protocol involves heteropolyanion-based catalyzed oxidation of alcohols to aldehydes with NaNO₃ as the oxidant followed by cyclocondensation with dicarbonyl compounds and urea or thiourea in a two-step, one-pot manner. Compatibility with different functional groups, good to excellent yields and reusable cataly  ...[more]

Similar Datasets

| S-EPMC7603249 | biostudies-literature
| S-EPMC6331848 | biostudies-other
| S-EPMC6972632 | biostudies-literature
| S-EPMC3008624 | biostudies-literature
| S-EPMC11357439 | biostudies-literature
| S-EPMC6689602 | biostudies-literature
| S-EPMC2649439 | biostudies-literature
| S-EPMC5505966 | biostudies-literature
| S-EPMC9122962 | biostudies-literature
| S-EPMC5099407 | biostudies-literature