Efficient Conversion of Biginelli 3,4-Dihydropyrimidin-2(1H)-one to Pyrimidines via PyBroP-Mediated Coupling
Author:
Affiliation:
1. Johnson & Johnson Pharmaceutical Research and Development, LLC, 1000 Route 202, Raritan, New Jersey 08869 %fkang@prdus.jnj.com
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo040281j
Reference38 articles.
1. 100 years of the biginelli dihydropyrimidine synthesis
2. Recent Advances in the Biginelli Dihydropyrimidine Synthesis. New Tricks from an Old Dog
3. A New Substrate for the Biginelli Cyclocondensation: Direct Preparation of 5-Unsubstituted 3,4-Dihydropyrimidin-2(1H)-ones from a β-Keto Carboxylic Acid
4. New Regioselective Multicomponent Reaction: One Pot Synthesis of Spiro Heterobicyclic Aliphatic Rings
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