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Peroxidation of 3,4-dihydro-1,4-benzoxazin-2-ones
Chemical Communications ( IF 4.9 ) Pub Date : 2020/02/26 , DOI: 10.1039/c9cc09778c
Jie Wang 1, 2, 3, 4, 5 , Xiazhen Bao 1, 2, 3, 4, 5 , Jiayuan Wang 1, 2, 3, 4, 5 , Congde Huo 1, 2, 3, 4, 5
Affiliation  

The sp3-C–H peroxidation of 3,4-dihydro-1,4-benzoxazin-2-ones was achieved under mild and simple catalyst-free reaction conditions. A range of biologically important alkylated benzoxazinone peroxides are synthesized in high yield with a good functional group tolerance. The C(sp3)-OO bond was constructed efficiently and could be further converted into C(sp3)–C(sp3), C(sp3)–C(sp2), C(sp3)–C(sp), C–P and C[double bond, length as m-dash]O bonds by late-stage functional group transformations.

中文翻译:

3,4-二氢-1,4-苯并恶嗪-2-酮的过氧化

3,4-二氢-1,4-苯并恶嗪-2-酮的sp 3 -C–H过氧化是在温和且简单的无催化剂条件下完成的。以高收率和良好的官能团耐受性合成了一系列生物学上重要的烷基化过氧化苯并恶嗪酮过氧化物。C(sp 3)-OO键结构有效,可以进一步转换为C(sp 3)–C(sp 3),C(sp 3)–C(sp 2),C(sp 3)–C( sp),C–P和C [双键,长度为m-破折号]O键通过后期官能团转化而形成。
更新日期:2020-04-03
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