620152-24-1Relevant academic research and scientific papers
Chemoselective Nucleophilic Attack on N-Acyl Derivatives of (S)-Ethyl 4,4-Dimethyl Pyroglutamate (DMPG)
Mantecon, Susana,Vaquero, Juan J.,Alvarez-Builla, Julio,De La Puente, Maria Luz,Espinosa, Juan F.,Ezquerra, Jesus
, p. 3791 - 3794 (2007/10/03)
(Matrix presented) Heteronucleophiles and C-nucleophiles chemoselectively react with N-acyl (S)-ethyl 4,4-dimethyl pyroglutamate (DMPG) affording esters, amides, and ketones in high yield. The intramolecular process allows the stereoselective formation of β-hydroxy acids likely by formation and ring opening of the corresponding β-lactones.
Aryl and heteroarylcylopropyl oxime ethers and their use as fungicides and insecticides
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, (2008/06/13)
Certain cyclopropyl oxime ethers substituted by aryl and heterocyclic moieties possess broad spectrum fungicidal and insecticidal properties. These compounds are disclosed along with compositions containing these compounds and methods for controlling fungi and insects by the use of a fungitoxic or insecticidal amount of these compounds.
Aryl and heteroarylcyclopropyl oxime ethers and their use as fungicides and insecticides
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, (2008/06/13)
Certain cyclopropyl oxime ethers substituted by aryl and heterocyclic moieties possess broad spectrum fungicidal and insecticidal properties. These compounds are disclosed along with compositions containing these compounds and methods for controlling fung
