Reactions of isoquinoline derivatives with pyridinium salts yielding 4-naphthylpyridines
S P Gromov
1
,
Publication type: Journal Article
Publication date: 2004-04-01
scimago Q3
SJR: 0.305
CiteScore: 2.8
Impact factor: —
ISSN: 10665285, 15739171
General Chemistry
Abstract
Regiospecific introduction of the 2-naphthyl residue into position 4 of the pyridine ring occurs in the reactions of isoquinolinium salts with 4-methylpyridinium salts through the intermolecular transformation of the isoquinoline bicyclic system involving the methyl group of the pyridinium salt. The reaction occurs under the action of methylammonium sulfite in an aqueous medium on heating. This method provides ring transformation not only for isoquinolinium salts but even for unsubstituted isoquinoline.
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Gromov S. P. et al. Reactions of isoquinoline derivatives with pyridinium salts yielding 4-naphthylpyridines // Russian Chemical Bulletin. 2004. Vol. 53. No. 4. pp. 901-905.
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Gromov S. P., Fomina M. V. Reactions of isoquinoline derivatives with pyridinium salts yielding 4-naphthylpyridines // Russian Chemical Bulletin. 2004. Vol. 53. No. 4. pp. 901-905.
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TY - JOUR
DO - 10.1023/B:RUCB.0000037861.00184.82
UR - http://link.springer.com/10.1023/B:RUCB.0000037861.00184.82
TI - Reactions of isoquinoline derivatives with pyridinium salts yielding 4-naphthylpyridines
T2 - Russian Chemical Bulletin
AU - Gromov, S P
AU - Fomina, M V
PY - 2004
DA - 2004/04/01
PB - Springer Nature
SP - 901-905
IS - 4
VL - 53
SN - 1066-5285
SN - 1573-9171
ER -
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BibTex (up to 50 authors)
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@article{2004_Gromov,
author = {S P Gromov and M V Fomina},
title = {Reactions of isoquinoline derivatives with pyridinium salts yielding 4-naphthylpyridines},
journal = {Russian Chemical Bulletin},
year = {2004},
volume = {53},
publisher = {Springer Nature},
month = {apr},
url = {http://link.springer.com/10.1023/B:RUCB.0000037861.00184.82},
number = {4},
pages = {901--905},
doi = {10.1023/B:RUCB.0000037861.00184.82}
}
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MLA
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Gromov, S. P., et al. “Reactions of isoquinoline derivatives with pyridinium salts yielding 4-naphthylpyridines.” Russian Chemical Bulletin, vol. 53, no. 4, Apr. 2004, pp. 901-905. http://link.springer.com/10.1023/B:RUCB.0000037861.00184.82.
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