Dix, Stefan; Jakob, Michael; Hopkinson, Matthew N. published the artcile< Deoxytrifluoromethylthiolation and Selenylation of Alcohols by Using Benzothiazolium Reagents>, Related Products of 52244-70-9, the main research area is trifluoromethylthio methylbenzothiazolium triflate aliphatic alc deoxytrifluoromethylthiolation; trifluoromethylselenyl methylbenzothiazolium triflate aliphatic alc deoxytrifluoromethylselenylation; alcohols; fluorine; reagent development; trifluoromethylselenyl group; trifluoromethylthio group.
Aliphatic compounds substituted with medicinally important trifluoromethylthio (SCF3) and trifluoromethylselenyl (SeCF3) groups were synthesized directly from alcs. by using the new benzothiazolium salts BT-SCF3 and BT-SeCF3. These bench-stable fluorine-containing reagents are facile to use and can be prepared in two steps from non-fluorinated heteroaromatic starting materials. To the best of our knowledge, these are the first reported examples in which the metal-free deoxytrifluoromethylthiolation process and similarly efficient trifluoromethylselenylation reactions proceeded under mild conditions using BT-SCF3 and BT-SeCF3 resp.
Chemistry – A European Journal published new progress about Aliphatic alcohols Role: RCT (Reactant), RACT (Reactant or Reagent). 52244-70-9 belongs to class ethers-buliding-blocks, and the molecular formula is C11H16O2, Related Products of 52244-70-9.
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem