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  4. The metalation of fluoroanisoles: optional regioselectivity due to metal mediated control
 
research article

The metalation of fluoroanisoles: optional regioselectivity due to metal mediated control

Katsoulos, Georges
•
Takagishi, Sadahito
•
Schlosser, Manfred  
1991
Synlett

2- And 4-Fluoroanisole undergo hydrogen/metal exchange at the position next to the alkoxy moiety if n-BuLi or tert-BuLi is used and at the position next to the halogen atom if the stoichiometric mixt. of butyllithium and potassium tert-butoxide serves as the reagents. 3-Fluoroanisole is always attacked at the position flanked by the 2 hetero-substituents. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1055/s-1991-34754
Author(s)
Katsoulos, Georges
•
Takagishi, Sadahito
•
Schlosser, Manfred  
Date Issued

1991

Published in
Synlett
Issue

10

Start page

731

End page

732

Subjects

Carboxylation (of lithiated fluoroanisoles); Regiochemistry (of lithiation of fluoroanisoles with butyllithium); Metalation (regioselective

•

of fluoroanisoles with butyllithium)

•

metalation flouroanisole regioselective

Note

CAN 116:20731

25-9

Benzene, Its Derivatives, and Condensed Benzenoid Compounds

Inst. Chim. Org.,Univ. Lausanne,Lausanne,Switz.

Journal

written in English.

68359-59-1P; 137654-22-9P (2-Fluoro-5-phenoxybenzoic acid) Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of, from regioselective lithiation and carboxylation of Ph fluorophenyl ether); 367-83-9P (2-Fluoro-5-methoxybenzoic acid); 394-04-7P (5-Fluoro-2-methoxybenzoic acid); 106428-05-1P (3-Fluoro-2-methoxybenzoic acid); 137654-20-7P (2-Fluoro-3-methoxybenzoic acid); 137654-21-8P (2-Fluoro-6-methoxybenzoic acid) Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of, from regioselective lithiation and carboxylation of fluoroanisole); 321-28-8 (2-Fluoroanisole); 330-84-7; 456-49-5 (3-Fluoroanisole); 459-60-9 (4-Fluoroanisole) Role: RCT (Reactant), RACT (Reactant or reagent) (regioselective lithiation and carboxylation of); 109-72-8P (Butyllithium) Role: RCT (Reactant), PREP (Preparation), RACT (Reactant or reagent) (regioselective lithiation by, of fluoroanisoles); 594-19-4 (tert-Butyllithium); 598-30-1 Role: RCT (Reactant), RACT (Reactant or reagent) (regioselective lithiation by, of fluoroanisoles)

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSCO  
Available on Infoscience
March 3, 2006
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/226873
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