A New Substrate for the Biginelli Cyclocondensation: Direct Preparation of 5-Unsubstituted 3,4-Dihydropyrimidin-2(1H)-ones from a β-Keto Carboxylic Acid
✍ Scribed by Bussolari, Jacqueline C.; McDonnell, Patricia A.
- Book ID
- 115542949
- Publisher
- American Chemical Society
- Year
- 2000
- Tongue
- English
- Weight
- 49 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0022-3263
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
## Abstract A novel __Biginelli__‐like cyclocondensation reaction is efficiently catalyzed by iodotrimethylsilane (Me~3~SiI) in MeCN. The reaction proceeds at room temperature by a three‐component one‐pot condensation of ketones with aldehydes and urea to afford 5‐unsubstituted 3,4‐dihydropyrimidin
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.