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Front Cover: A Convenient Palladium‐Catalyzed Aminocarbonylation of Aryl Iodides to Primary Amides under Gas‐Free Conditions (Eur. J. Org. Chem. 48/2017)
Author(s) -
Qi Xinxin,
Ai HanJun,
Cai ChuangXu,
Peng JinBao,
Ying Jun,
Wu XiaoFeng
Publication year - 2017
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201701686
Subject(s) - chemistry , palladium , aryl , phosphine , formic acid , catalysis , organic chemistry , primary (astronomy) , ligand (biochemistry) , ammonium bicarbonate , medicinal chemistry , combinatorial chemistry , raw material , biochemistry , alkyl , physics , receptor , astronomy
The Front Cover shows sweet cherries, which contain amides. In this picture, the two cherries represent formic acid and ammonium bicarbonate, which are sources of CO and NH 3 , respectively. In the presence of palladium and the phosphine ligand, aryl iodides were transformed into the corresponding primary amides under gas‐free conditions. More information can be found in the Communication by X.‐F. Wu et al.