Facile aromatization of 3,4-dihydropyrimidin-2(1H)-ones (DHPMs) by iodine
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference41 articles.
1. Highly Enantioseletive Biginelli Reaction Using a New Chiral Ytterbium Catalyst: Asymmetric Synthesis of Dihydropyrimidines
2. Highly Enantioselective Organocatalytic Biginelli Reaction
3. Highly Chemoselective Multicomponent Biginelli-Type Condensations of Cycloalkanones, Urea or Thiourea and Aldehydes
4. Concise Synthesis of Guanidine-Containing Heterocycles Using the Biginelli Reaction
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1. A Green Chemical Approach for Iodination of Pyrimidine Derivatives by Mechanical Grinding under Solvent-Free Conditions;Molecules;2022-09-27
2. Emerging Role of Green Oxidant I2/DMSO in Organic Synthesis;Current Organic Synthesis;2018-08-29
3. Advances in the Oxidation of Biginelli Compounds;Current Organic Chemistry;2018-05-31
4. In situ formed tert-butyl hypoiodite as an efficient oxidant for rapid, room temperature, metal-free aromatization of Biginelli 3,4-dihydropyrimidin-2(1H)-ones under basic conditions;Arkivoc;2016-04-19
5. Microwave-assisted and iodine mediated synthesis of 5-n-alkyl-cycloalkane[d]-pyrazolo[3,4-b]pyridines from 5-aminopyrazoles and cyclic ketones;Tetrahedron Letters;2014-03
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