Chalcogenative spirocyclization of N-aryl propiolamides with diselenides/disulfides promoted by Selectfluor

JW Yuan, GC Huang, LL Wang, XY Wang… - … für Naturforschung B, 2022 - degruyter.com
A practical and efficient synthetic route to construct a variety of 3-arylselenenyl/3-arylthio
spiro [4.5] trienones was developed using Selectfluor reagent as a mild oxidant. This …
被引用次数：4 相关文章

Chalcogenative spirocyclization of N-aryl propiolamides with diselenides/disulfides promoted by Selectfluor.

JW Yuan, GC Huang, LL Wang… - … Naturforschung B: A …, 2022 - search.ebscohost.com
A practical and efficient synthetic route to construct a variety of 3-arylselenenyl/3-arylthio
spiro [4.5] trienones was developed using Selectfluor reagent as a mild oxidant. This …

Chalcogenative spirocyclization of N-aryl propiolamides with diselenides/disulfides promoted by Selectfluor

JW Yuan, GC Huang, LL Wang, XY Wang, LR Yang… - Z …, 2022 - degruyter.com
A practical and efficient synthetic route to construct a variety of 3-arylselenenyl/3-arylthio
spiro [4.5] trienones was developed using Selectfluor reagent as a mild oxidant. This …

Chalcogenative spirocyclization of N-aryl propiolamides with diselenides/disulfides promoted by Selectfluor

JW Yuan, GC Huang, LL Wang… - … für Naturforschung B, 2022 - ingentaconnect.com
A practical and efficient synthetic route to construct a variety of 3-arylselenenyl/3-arylthio
spiro [4.5] trienones was developed using Selectfluor reagent as a mild oxidant. This …

[引用][C] Chalcogenative spirocyclization of N-aryl propiolamides with diselenides/disulfides promoted by Selectfluor

JW Yuan, GC Huang, LL Wang, XY Wang, LR Yang… - 2022