13787-96-7Relevant articles and documents
Hydrazones as Substrates in the Synthesis of Isoxazolidines via a KOH-Promoted One-Pot Three-Component Cycloaddition with Nitroso Compounds and Olefins
Chen, Wenwen,Li, Wenhui,Li, Xing,Lin, Jianying,Wei, Wen-Long,Zhai, Pingan
, p. 17710 - 17721 (2021/12/09)
Hydrazones have been employed as the starting materials in a KOH-mediated one-pot three-component cycloaddition with readily accessible nitroso compounds and olefins to construct various isoxazolidines. Compared with diazo compounds as starting materials, this methodology could afford a wider range of products in good to excellent yields and diastereoselectivities for most substrates, and hydrazones are cheaper, more accessible, and safer substrates. The experimental study shows that the choice of suitable hydrazones is crucial.
Conversion of nitrosobenzenes to isoxazolidines: An efficient cascade process utilizing reactive nitrone intermediates
Kang, Jun Yong,Bugarin, Alejandro,Connell, Brian T.
supporting information; experimental part, p. 3522 - 3524 (2009/02/05)
Reactive nitrones can be generated directly in situ by an unusual reaction of nitrosobenzene with styrene. The Royal Society of Chemistry.
Novel Catalytic System consisting of a 3,3'-Tetramethylene-bridged 4-Methylthiazolium Salt Leading to the Partial Reduction of Nitrobenzene with Benzaldehyde to a Nitrone
Inoue, Hiroo,Tamura, Shigeo
, p. 141 - 142 (2007/10/02)
A 3,3'-tetramethylene-bridged 4-methylthiazolium salt catalyses the reduction of nitrobenzene with benzaldehyde and triethylamine in methanol-water to give a nitrone.
