169762-37-2Relevant academic research and scientific papers
A mild catalytic synthesis of 2-oxazolines: Via oxetane ring-opening: Rapid access to a diverse family of natural products
Huang, Hai,Yang, Wen,Chen, Zuliang,Lai, Zengwei,Sun, Jianwei
, p. 9586 - 9590 (2019/11/05)
A new catalytic protocol for the expedient synthesis of oxazolines from oxetanes is disclosed. This mild process complements the conventional oxazoline synthesis based on non-catalytic cyclization of β-hydroxy or unsaturated amides. It is also a new addition to the reactivity profile of oxetanes leading to heterocycles. In the presence of In(OTf)3, various 3-amido oxetanes underwent smooth intramolecular cyclization to form the corresponding 2-oxazolines, including some valuable oxazoline-based bidentate ligands. This protocol also provides rapid access to various natural products and antibacterial molecules.
Phenylthio-oxazoline compounds and their use as pesticides
-
, (2008/06/13)
The invention relates to new phenylthio-oxazoline derivatives of the formula (I) in which A represents optionally substituted phenyl; B represents optionally substituted phenyl; D represents hydrogen or alkyl; and n represents 0, 1 or 2; to a plurality of
Oxazoline derivative, its production and its use
-
, (2008/06/13)
An oxazoline derivative having the formula: STR1 which is useful for control of insects, mites and/or ticks. R1 is H, halo, (halo) alkyl, alkoxy alkyl, (halo) alkoxy alkyl, (halo) alkyl thio, (halo) cycloalkyl, alkylcycloalkyl, (halo) cycloalkoxy, alkylcycloalkoxy or (R5) phenyl, phenoxyl or phenylthio or (R5) pyridyl, pyridoxyl or pyridylthio, R3 is H or methyl, R4 is phenyl or mono or disubstituted phenyl.
