Radical fluorosulfonylation is emerging as an appealing approach for the synthesis of
sulfonyl fluorides, which have widespread applications in many fields, in particular in the …

Although nature uses the aqueous environment in most of its chemical/biochemical
transformations, water as solvent was totally neglected in organic transformations till the end …

An electroreductive strategy for radical hydroxyl fluorosulfonylation of alkenes with sulfuryl
chlorofluoride and molecular oxygen from air is described. This mild protocol displays …

The influence of added surfactant to aqueous reaction mixtures containing various IREDs
has been determined. Just the presence of a nonionic surfactant tends to increase both rates …

A visible-light-mediated catalyst-and additive-free method for radical ring-opening
fluorosulfonylation of methylenecyclobutanols is reported. Sulfuryl chlorofluoride acts as a …

Naturally occurring phospholipids, such as phosphatidyl glycerol (PG), are gaining interest
due to the roles they play in disease mechanisms. To elucidate the metabolism of PG, an …

The accidental discovery of crown ethers by Pedersen generated a new field of research for
scientists [1–8]. Crown ethers are macrocyclic polyethers ranging from 3 to 20 oxygen atoms …

The world of modern organic chemistry, a very traditional but unsustainable 200-year-old
discipline, relies heavily on the use of environmentally harmful chemicals. From the 12 …

[1309573‐60‐1] C66H120O21 (MW 1249.6) InChI= 1S/C65H118O21/c1‐54 (2) 15‐16‐56
(4) 13‐10‐12‐55 (3) 14‐11‐20‐65 (8) 21‐19‐60‐59 (7) 63 (57 (5) 58 (6) 64 (60) 86‐65) 85 …