65269-96-7Relevant articles and documents
An Easy, General and Practical Method for the Construction of Alkyl Sulfonyl Fluorides
Zhang, Xu,Fang, Wan-Yin,Lekkala, Ravindar,Tang, Wenjian,Qin, Hua-Li
supporting information, p. 3358 - 3363 (2020/07/13)
A visible light-induced reductive addition of 1°, 2° and 3° alkyl iodides to ethenesulfonyl fluoride, employing Hantzsch ester as a hydrogen source at room temperature was developed. This method featured a wide substrate scope and great functional group compatibility, providing facile and robust process to alkyl sulfonyl fluorides including enzyme inhibitors, natural products and drugs derivatives in up to 99percent yield. Further derivatization of resultant aliphatic sulfonyl fluorides was also achieved through sulfur fluoride exchange (SuFEx) reactions to deliver sulfonates and sulfonamides as privileged motifs for medicinal chemistry. (Figure presented.).