A versatile synthesis of new pyrimidinyl nitronyl nitroxides
Chemical Communications2003Iss. 21, pp. 2722–2723
Citations Over Time
Abstract
Pyrimidinyl nitronyl nitroxides where the bis-N-oxy fragment is included in a six-membered ring were prepared from diacetonamine by a sequence of reactions including a Grignard reaction, a Ritter reaction and oxidation of the intermediate pyrimidine; the properties of the 2-phenyl-substituted representative are fully described.
Related Papers
- → Recent Applications of Ritter Reactions in Organic Syntheses(2020)52 cited
- → Ritter-type Reactions(1991)42 cited
- → ChemInform Abstract: Safe and Efficient Ritter Reactions in Flow.(2011)
- → ChemInform Abstract: One‐Pot Protocol to Synthesize N‐(β‐Nitro)amides by Tandem Henry/Ritter Reaction.(2015)
- → Tropylium-Catalyzed Ritter Reaction under Flow Conditions(2022)