z-logo
Premium
Pd‐Catalyzed Cross‐Coupling of Organozinc Pivalates with Arene Thianthrenium Salts Under Ball‐Milling Conditions
Author(s) -
Čarný Tomáš,
Mart Mehmet,
Blauciak Michal,
Steinhüblová Barbora,
Šebesta Radovan
Publication year - 2025
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.202500373
Subject(s) - ball mill , catalysis , ball (mathematics) , chemistry , coupling (piping) , heterogeneous catalysis , polymer chemistry , materials science , chemical engineering , inorganic chemistry , organic chemistry , metallurgy , engineering , geometry , mathematics
Abstract Cross‐coupling reactions are important tools in the synthesis of complex molecules. In this work, we show that the Pd‐catalyzed cross‐coupling of aryl zinc pivalates with aryl thianthrenium salts offers a greener way to realize Negishi cross‐coupling reaction. Our results show that organozinc pivalates are air‐stable alternatives to classical organozinc halides and are suitable for mechanochemical reactions. Arene thianthrenium salts are alternative electrophilic reagents that are more compatible and selective than traditional organic halides. Moreover, the majority of thianthrene can be recovered after the cross‐coupling reaction.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom