28883-94-5Relevant academic research and scientific papers
2 H-Azirines as Potential Bifunctional Chemical Linkers of Cysteine Residues in Bioconjugate Technology
Chen, Yang,Jiang, Yaojia,Loh, Teck-Peng,Sun, Wangbin,Wu, Jiamin,Yang, Wenjie
supporting information, p. 2038 - 2043 (2020/03/24)
2H-Azirine-2-caboxamides have been designed to perform as a new type of bifunctional thiol linker under very mild reaction conditions. The cleavage of a C-N double bond of 2H-azirine furnishes an amino amide functional group in situ through a thiol addition and ring-opening process. It works with a broad scope of thiols and 2H-azirines in the absence of any catalysts at room temperature. Cysteine-containing peptides have also been demonstrated to work efficiently in a completely water solution.
Synthetic method of alpha-amino acid derivative
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Paragraph 0021-0023; 0025, (2019/08/03)
The invention relates a synthetic method of an alpha-amino acid derivative. The synthetic method comprises the step of attacking carbon and nitrogen double bonds of an azacyclo-propylene compound which is taken as a raw material with a sulfhydryl compound
Hoveyda-Grubbs II Catalyst: A Useful Catalyst for One-Pot Visible-Light-Promoted Ring Contraction and Olefin Metathesis Reactions
Ge, Yun,Sun, Wangbin,Pei, Bingbing,Ding, Jia,Jiang, Yaojia,Loh, Teck-Peng
supporting information, p. 2774 - 2777 (2018/05/22)
A one-pot reaction to synthesize functionalized 2H-azirines through visible-light-mediated ring contraction and olefin metathesis of isoxazoles is described. Hoveyda-Grubbs II catalyst was found to function as a photocatalyst for these transformations, al
