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  4. Selective Functionalization of 2-Fluoropyridine, 2,3-Difluoropyridine, and 2,5-Difluoropyridine at Each Vacant Position
 
research article

Selective Functionalization of 2-Fluoropyridine, 2,3-Difluoropyridine, and 2,5-Difluoropyridine at Each Vacant Position

Bobbio, Carla
•
Schlosser, Manfred  
2005
The Journal of Organic Chemistry

The concept of "regioexhaustive substitution" has been successfully applied to 2-fluoro-, 2,3-difluoro-, and 2,5-difluoropyridine. All vacant positions were amenable to regioselective metalation and subsequent carboxylation by employing either chlorine as a neighboring site activating protective group or trimethylsilyl as a neighboring site screening protective group. In this way, approx. half a dozen fluorinated pyridinecarboxylic acids were derived from each starting material. [on SciFinder (R)]

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Type
research article
DOI
10.1021/jo047979h
Web of Science ID

WOS:000228367100016

Author(s)
Bobbio, Carla
Schlosser, Manfred  
Date Issued

2005

Published in
The Journal of Organic Chemistry
Volume

70

Issue

8

Start page

3039

End page

3045

Subjects

Protective groups (regioselective metalation and subsequent carboxylation of fluoropyridines by employing either chlorine as a neighboring site activating protective group or trimethylsilyl as a neighboring site screening protective group); Metalation (

•

fluoropyridine regioselective metalation carboxylation; pyridinecarboxylic acid fluoro prepn

Note

CAN 142:447088 27-16 Heterocyclic Compounds (One Hetero Atom) Institute of Chemical Sciences and Engineering (ISIC-BCh),Ecole Polytechnique Federale,Lausanne,Switz. Journal 0022-3263 written in English. 372-48-5 (2-Fluoropyridine); 994-30-9 (Chlorotriethylsilane); 1513-66-2 (2,3-Difluoropyridine); 84476-99-3 (2,5-Difluoropyridine) Role: RCT (Reactant), RACT (Reactant or reagent) (selective functionalization of 2-fluoropyridine, 2,3-difluoropyridine, and 2,5-difluoropyridine at each vacant position via regioselective metalation and subsequent carboxylation); 1480-64-4P (3-Chloro-2-fluoropyridine); 741683-19-2P; 851178-99-9P; 851179-03-8P; 851386-27-1P; 851386-28-2P; 851386-29-3P; 851386-30-6P; 851386-32-8P; 851386-34-0P; 851386-35-1P; 851386-36-2P; 851386-37-3P; 851386-40-8P; 851386-41-9P; 851386-42-0P; 851386-44-2P; 851386-46-4P; 851386-47-5P; 851386-48-6P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (selective functionalization of 2-fluoropyridine, 2,3-difluoropyridine, and 2,5-difluoropyridine at each vacant position via regioselective metalation and subsequent carboxylation); 393-55-5P (2-Fluoropyridine-3-carboxylic acid); 402-65-3P (2-Fluoropyridine-4-carboxylic acid); 402-69-7P (6-Fluoropyridine-2-carboxylic acid); 403-45-2P (6-Fluoropyridine-3-carboxylic acid); 851386-31-7P; 851386-33-9P; 851386-38-4P; 851386-39-5P; 851386-43-1P; 851386-45-3P Role: SPN (Synthetic preparation), PREP (Preparation) (selective functionalization of 2-fluoropyridine, 2,3-difluoropyridine, and 2,5-difluoropyridine at each vacant position via regioselective metalation and subsequent carboxylation)

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/20.500.14299/227041
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