85059-38-7Relevant academic research and scientific papers
Divergent Synthesis of Enantioenriched β-Functional Amines via Desymmetrization of meso-Aziridines with Isocyanides
Li, Xiangqiang,Xiong, Qian,Guan, Mingming,Dong, Shunxi,Liu, Xiaohua,Feng, Xiaoming
supporting information, p. 6096 - 6101 (2019/08/20)
A highly enantioselective ring-opening desymmetrization of meso-aziridines with isocyanides was achieved in the presence of a chiral N,N′-dioxide/Mg(OTf)2 complex. The in situ generated chiral 1,4-zwitterionic intermediates were successfully trapped by intramolecular oxygen- and carbon-based nucleophiles or exogenous H2O and TMSN3, enabling a collective synthesis of various chiral vicinal amino-oxazoles, spiroindolines, β-amino amides, and tetrazole derivative in moderate to high yields with excellent enantioselectivities.
Multicomponent synthesis of epoxy-tetrahydronaphthyridine and structural diversification by subsequent fragmentation
Fayol, Aude,Zhu, Jieping
, p. 11511 - 11519 (2007/10/03)
Three-component reaction of an α-isocyanoacetamide 7, an homoallylamine 8 and an aldehyde 9 in methanol at room temperature provides oxa-bridged tricycle 4 in good to excellent yield as a mixture of two separable diastereoisomers. In this one-pot multicom
Antifungal Activities of &α-Isocyano-&β-phenylpropionamides
Takiguchi, Kazuo,Yamada, Kunihiko,Suzuki, Mamoru,Nunami, Ken-ichi,Hayashi, Kimiaki,Matsumoto, Kazuo
, p. 77 - 82 (2007/10/02)
A variety of α-isocyano-β-phenylpropionamides were synthesized and their inhibitory activities examined against Sphaerotheca fuliginea and Cladosporium fulvum.Among them, N-cyclohexyl-α-isocyano-β-phenylpropionamide (3c) was chosen as the first candidate
