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Frontispiece: Rapid Deoxyfluorination of Alcohols with N ‐Tosyl‐4‐chlorobenzenesulfonimidoyl Fluoride (SulfoxFluor) at Room Temperature
Author(s) -
Guo Junkai,
Kuang Cuiwen,
Rong Jian,
Li Lingchun,
Ni Chuanfa,
Hu Jinbo
Publication year - 2019
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201983063
Subject(s) - reagent , tosyl , ball (mathematics) , fluoride , chemistry , organic chemistry , inorganic chemistry , mathematics , geometry
The new deoxyfluorination reagent SulfoxFluor is represented by a fast‐running car. SulfoxFluor is capable of rapid fluorination of various alcohols. The chemical structure is drawn on the car. Shown at bottom right of the graphic is the ball‐and‐stick model. The traffic sign shows three directions (substrates): left for diols, middle for primary alcohols, and right for secondary alcohols. A representative fluorinated product is shown on each road (direction). For more details, see the Communication by C. Ni, J. Hu and co‐workers on page 7259 ff.