Product Details of 696-59-3In 2021 ,《Primary Sulfonamide Functionalization via Sulfonyl Pyrroles: Seeing the N-Ts Bond in a Different Light》 was published in Chemistry – A European Journal. The article was written by Ozaki, Tomoya; Yorimitsu, Hideki; Perry, Gregory J. P.. The article contains the following contents:
Easy-to-access arylsulfonyl pyrroles I (R = 4-MeC6H4, 4-FC6H4, etc.) as synthetic linchpins for sulfonamides RC6H4S(O)2R1 (R1 = CH3, F, 5-(trifluoromethyl)pyridin-2-yl, etc.) functionalization have been described. The versatility of the sulfonyl pyrrole unit is shown by generating a variety of products through chem., electrochem. and photochem. pathways. Preliminary results on the direct functionalization of primary sulfonamides are also provided, which may lead to new modes of activation. In the part of experimental materials, we found many familiar compounds, such as 2,5-Dimethoxytetrahydrofuran(cas: 696-59-3Product Details of 696-59-3)
2,5-Dimethoxytetrahydrofuran(cas: 696-59-3) is a member of ether. When aromatic ethers are exposed to halogen in the presence or absence of a catalyst, they undergo halogenation, such as bromination.Product Details of 696-59-3
Referemce:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem