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Transformations of N -arylpropiolamides to indoline-2,3-diones and acids via C≡C triple bond oxidative cleavage and C(sp 2 )–H functionalization
Science China Chemistry ( IF 9.6 ) Pub Date : 2019-10-22 , DOI: 10.1007/s11426-019-9633-x
Ming-Bo Zhou , Yang Li , Xuan-Hui Ouyang , Jin-Heng Li

A new palladium-catalyzed oxidative conversion of N-arylpropiolamides and H2O to various indoline-2,3-diones and acids through the C≡C triple bond cleavage and C(sp2)–H functionalization is described, which is promoted by a cooperative action of catalytic CuBr2, 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) and O2. The method provides a practical tool for transformations of alkynes by means of a C–H functionalization strategy, which enables the formation of one C–C bond and multiple C–O bonds in a single reaction with high substrates compatibility and excellent functional group tolerance.

中文翻译:

通过C≡C三键氧化裂解和C(sp 2)-H功能化将N-芳基丙酰胺转化为吲哚啉2,3-二酮和酸

描述了通过C tripleC三键裂解和C(sp 2)-H官能化作用,将新的钯催化的N-丙酰胺和H 2 O氧化转化为各种二氢吲哚-2,3-二酮和酸的过程,这一点受到促进。催化的CuBr的协作动作2,2,2,6,6-四甲基-1-哌啶氧(TEMPO)和O 2。该方法通过C–H官能化策略为炔烃的转化提供了实用的工具,该方法可在单个反应中形成一个C–C键和多个C–O键,并具有高的底物相容性和出色的官能团耐受性。
更新日期:2019-10-25
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