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1
Perhalopyridines: Synthesis and Synthetic Utility
Bentham Books
Ranjbar-Karimi R.
,
Poorfreidoni A.
synthesis
reaction
dx.doi.org
pentafluoropyridine
synthetic
perhalopyridines
utility
reactions
compounds
pyridine
pentachloropyridine
karimi
ranjbar
nucleophilic
poorfreidoni
nucleophiles
derivatives
perfluoropyridines
substitution
tetrachloro
soc
presence
pmid
substituted
tetrafluoropyridine
products
systems
formation
aromatic
sodium
fluorine
pentabromopyridine
chemistry
pyridines
heterocyclic
nucleophile
bond
tetrachloropyridine
addition
coupling
obtained
oxidation
product
fluorinated
nitrogen
perchloropyridines
salt
atom
centered
lithium
Anno:
2020
Lingua:
english
File:
PDF, 13.49 MB
I tuoi tag:
0
/
0
english, 2020
2
Perhalopyridines: Synthesis and Synthetic Utility
Bentham Science Publishers
Reza Ranjbar-Karimi
,
Alireza Poorfreidoni
synthesis
reaction
dx.doi.org
pentafluoropyridine
synthetic
perhalopyridines
utility
reactions
compounds
pyridine
pentachloropyridine
karimi
ranjbar
nucleophilic
poorfreidoni
nucleophiles
derivatives
perfluoropyridines
substitution
tetrachloro
soc
presence
pmid
substituted
tetrafluoropyridine
products
systems
formation
aromatic
sodium
fluorine
pentabromopyridine
chemistry
pyridines
heterocyclic
nucleophile
bond
tetrachloropyridine
addition
coupling
obtained
oxidation
product
fluorinated
nitrogen
perchloropyridines
salt
atom
centered
lithium
Anno:
2020
Lingua:
english
File:
PDF, 18.79 MB
I tuoi tag:
0
/
0
english, 2020
3
Organometallic Fluorine Chemistry
Springer International Publishing
Thomas Braun
,
Russell P. Hughes (eds.)
bond
reaction
catalyzed
fluorination
complexes
complex
activation
fluoride
aryl
reactions
transition
fluorous
formation
reported
hdf
fluorine
soc
bonds
equiv
catalytic
mol
palladium
synthesis
ligand
groups
fluorinated
oxidative
reagents
elimination
catalyst
mediated
cf3
mechanism
addition
coupling
reactivity
hydrodefluorination
nucleophilic
alkyl
ligands
product
presence
species
chemistry
electrophilic
nickel
intermediate
radical
electron
aromatic
Anno:
2015
Lingua:
english
File:
PDF, 14.33 MB
I tuoi tag:
0
/
0
english, 2015
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