Sun, Wei’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2022 | 10541-78-3

Chemical Communications (Cambridge, United Kingdom) published new progress about Aromatic amines Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 10541-78-3 belongs to class ethers-buliding-blocks, and the molecular formula is C8H11NO, Product Details of C8H11NO.

Sun, Wei; Raimbach, William A. T.; Elliott, Luke D.; Booker-Milburn, Kevin I.; Harrowven, David C. published the artcile< New approaches to ondansetron and alosetron inspire a versatile, flow photochemical method for indole synthesis>, Product Details of C8H11NO, the main research area is aryl amino cycloalkenone iodine catalyst oxidative photocyclization; tetrahydro cycloalkaindolone preparation; arylamino alkenone iodine catalyst oxidative photocyclization; indolyl alkenone preparation.

An oxidative photocyclization of N-arylenaminones to indoles was described, that mirrored the Fischer indole synthesis but used anilines in place of arylhydrazines. Its value was exemplified with new approaches to the WHO-listed APIs ondansetron and alosetron.

Chemical Communications (Cambridge, United Kingdom) published new progress about Aromatic amines Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 10541-78-3 belongs to class ethers-buliding-blocks, and the molecular formula is C8H11NO, Product Details of C8H11NO.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem