Oxidative dehydrogenative [3+3] annulation of benzylhydrazines with N-sulfonylaziridines is described.A series of complex tetrahydro-1,2,4-triazines were produced under mild reaction conditions.
An oxidative tandem(4+2)-cyclization/aromatization of N-aryl glycine derivatives with electron-deficient alkenes was first achieved using Ru(bpy)_(3)Cl_(2) as a photocatalyst and TBHP as an oxidant in combination with...An oxidative tandem(4+2)-cyclization/aromatization of N-aryl glycine derivatives with electron-deficient alkenes was first achieved using Ru(bpy)_(3)Cl_(2) as a photocatalyst and TBHP as an oxidant in combination with visible-light irradiation by blue LEDs.One-electron oxidation and the followingα-deprotonation of glycine derivatives affordα-amino alkyl radicals,which were then trapped by electrophilic maleimides.As an atom-economic and efficient method,a variety of pyrrolo[3,4-c]quinoline-1,3-diones have been obtained in good yields under mild reaction conditions.展开更多
A new protocol for the NiC12-catalyzed cross-electrophile coupling of aryl bromides with pyrimidin-2-yl tosyl- ates to give the corresponding C2-arylation pyrimidine derivatives has been developed. This study provides...A new protocol for the NiC12-catalyzed cross-electrophile coupling of aryl bromides with pyrimidin-2-yl tosyl- ates to give the corresponding C2-arylation pyrimidine derivatives has been developed. This study provides an improvement over previous methods by using pyrimidin-2-yl tosylates instead of halides as coupling partners that are stable and easily available.展开更多
Summary of main observation and conclusion A Cu(OAc)2/DDQ/DTBP/Py system catalyzed oxidative dehydrogenative silylation-alkenation tandem reaction of readily available alkyl aromatic compounds with silanes was establi...Summary of main observation and conclusion A Cu(OAc)2/DDQ/DTBP/Py system catalyzed oxidative dehydrogenative silylation-alkenation tandem reaction of readily available alkyl aromatic compounds with silanes was established.A variety of functionalized alkenyl organosilicon compounds were provided in good to high yields with a totalβ-(E)selectivity.The control experiments revealed that the transformation might proceed through a radical pathway.展开更多
基金We thank the National Natural Science Foundation of China (No. 21562037) for financially supporting this work.
文摘Oxidative dehydrogenative [3+3] annulation of benzylhydrazines with N-sulfonylaziridines is described.A series of complex tetrahydro-1,2,4-triazines were produced under mild reaction conditions.
基金We thank the National Natural Science Foundation of China(No.21961033)for financially supporting this work.
文摘An oxidative tandem(4+2)-cyclization/aromatization of N-aryl glycine derivatives with electron-deficient alkenes was first achieved using Ru(bpy)_(3)Cl_(2) as a photocatalyst and TBHP as an oxidant in combination with visible-light irradiation by blue LEDs.One-electron oxidation and the followingα-deprotonation of glycine derivatives affordα-amino alkyl radicals,which were then trapped by electrophilic maleimides.As an atom-economic and efficient method,a variety of pyrrolo[3,4-c]quinoline-1,3-diones have been obtained in good yields under mild reaction conditions.
基金We are thankful for the financial support from the National Natural Science Foundation of China （Nos. 21362032, 21362031 and 21562036） and Northwest Normal University （No. NWNU-LKQN- 15-1 ）.
文摘A new protocol for the NiC12-catalyzed cross-electrophile coupling of aryl bromides with pyrimidin-2-yl tosyl- ates to give the corresponding C2-arylation pyrimidine derivatives has been developed. This study provides an improvement over previous methods by using pyrimidin-2-yl tosylates instead of halides as coupling partners that are stable and easily available.
基金We thank the National Natural Science Foundation of China(No.21961033)for financially supporting this work.
文摘Summary of main observation and conclusion A Cu(OAc)2/DDQ/DTBP/Py system catalyzed oxidative dehydrogenative silylation-alkenation tandem reaction of readily available alkyl aromatic compounds with silanes was established.A variety of functionalized alkenyl organosilicon compounds were provided in good to high yields with a totalβ-(E)selectivity.The control experiments revealed that the transformation might proceed through a radical pathway.
