Erratum: Palladium-Catalyzed Carbonylative Reactions of 1-Bromo-2-fluorobenzenes with Various Nucleophiles: Effective Combination of Carbonylation and Nucleophilic Substitution (Chemistry - A European Journal (2014) 20 DOI: 10.1002/chem.201405221)

Full text of DOI:10.1002/chem.201504244

Contents
CORRIGENDUM
J. Chen, K. Natte, H. Neumann,
X.-F. Wu* ........................ 16107–16110
The authors found that the structures shown in Table 2 in their Communication are
incorrect. They should be chromenones, not isochromenones. The correct structures
for Table 2 are given below. The authors apologize for this mistake.
Palladium-Catalyzed Carbonylative
Reactions of 1-Bromo-2-fluoroben-
zenes with Various Nucleophiles:
Effective Combination of Carbonyla-
tion and Nucleophilic Substitution
Table 2. Palladium-catalyzed carbonylative synthesis of isochromeno-
nes.[a]
Chem. Eur. J., 2014, 20
DOI: 10.1002/chem.201405221
j, 40%
k, 40%
l, 34%
[a] Reaction conditions: 1-bromo-2-fluorobenzene (0.5 mmol), 2-phenyla-
cetophenone (1.0 equiv), [Pd(cinnamyl)Cl]2 (3 mol%), DPPB (9 mol%),
Cs2CO3 (3.0 equiv), DMAc (3 mL), CO (50 bar), 1408C, 40 h. Yield of the iso-
lated product.
Chem. Eur. J. 2015, 21, 17526 – 17542
17542
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