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Synthesis of 6H,7H-pyrido[2,1-a]isoquinolinium zwitterions from 6-nitro-2-polyfluoroalkylchromones and 1,3,3-trimethyl-3,4-dihydroisoquinolines. /
Sosnovskikh, V. Ya; Usachev, B. I.; Vshivkova, T. S. et al.
In:
Russian Chemical Bulletin, Vol. 63, No. 6, 01.01.2014, p. 1337-1343.
Research output: Contribution to journal › Article › peer-review
Harvard
Sosnovskikh, VY, Usachev, BI, Vshivkova, TS & Shklyaev, YV 2014, '
Synthesis of 6H,7H-pyrido[2,1-a]isoquinolinium zwitterions from 6-nitro-2-polyfluoroalkylchromones and 1,3,3-trimethyl-3,4-dihydroisoquinolines',
Russian Chemical Bulletin, vol. 63, no. 6, pp. 1337-1343.
https://doi.org/10.1007/s11172-014-0600-0
APA
Sosnovskikh, V. Y., Usachev, B. I., Vshivkova, T. S., & Shklyaev, Y. V. (2014).
Synthesis of 6H,7H-pyrido[2,1-a]isoquinolinium zwitterions from 6-nitro-2-polyfluoroalkylchromones and 1,3,3-trimethyl-3,4-dihydroisoquinolines.
Russian Chemical Bulletin,
63(6), 1337-1343.
https://doi.org/10.1007/s11172-014-0600-0
Vancouver
Author
BibTeX
@article{11545297aeb04e92a26596bfbee57191,
title = "Synthesis of 6H,7H-pyrido[2,1-a]isoquinolinium zwitterions from 6-nitro-2-polyfluoroalkylchromones and 1,3,3-trimethyl-3,4-dihydroisoquinolines",
abstract = "1,3,3-Trimethyl-3,4-dihydroisoquinolines and their crown-containing derivatives react with 6-nitro-2-polyfluoroalkylchromones in THF at room temperature with the formation of zwitterionic axially chiral 6H,7H-pyrido[2,1-a]isoquinolinium derivatives, which were converted to 2,6-diaryl-4-polyfluoroalkylpyridines, including those with the benzocrown-ether fragment. {\textcopyright} 2014 Springer Science+Business Media New York.",
keywords = "1 3 3-trimethyl-3 4-dihydroisoquinolines, 2 6-diaryl-4-poly-fluoroalkylpyridines, 2-polyfluoroalkylchromones, atropisomerism, benzocrown ethers, pyrido[2 1-a]isoquinolinium zwitterions",
author = "Sosnovskikh, {V. Ya} and Usachev, {B. I.} and Vshivkova, {T. S.} and Shklyaev, {Yu V.}",
year = "2014",
month = jan,
day = "1",
doi = "10.1007/s11172-014-0600-0",
language = "English",
volume = "63",
pages = "1337--1343",
journal = "Russian Chemical Bulletin",
issn = "1066-5285",
publisher = "Springer",
number = "6",
}
RIS
TY - JOUR
T1 - Synthesis of 6H,7H-pyrido[2,1-a]isoquinolinium zwitterions from 6-nitro-2-polyfluoroalkylchromones and 1,3,3-trimethyl-3,4-dihydroisoquinolines
AU - Sosnovskikh, V. Ya
AU - Usachev, B. I.
AU - Vshivkova, T. S.
AU - Shklyaev, Yu V.
PY - 2014/1/1
Y1 - 2014/1/1
N2 - 1,3,3-Trimethyl-3,4-dihydroisoquinolines and their crown-containing derivatives react with 6-nitro-2-polyfluoroalkylchromones in THF at room temperature with the formation of zwitterionic axially chiral 6H,7H-pyrido[2,1-a]isoquinolinium derivatives, which were converted to 2,6-diaryl-4-polyfluoroalkylpyridines, including those with the benzocrown-ether fragment. © 2014 Springer Science+Business Media New York.
AB - 1,3,3-Trimethyl-3,4-dihydroisoquinolines and their crown-containing derivatives react with 6-nitro-2-polyfluoroalkylchromones in THF at room temperature with the formation of zwitterionic axially chiral 6H,7H-pyrido[2,1-a]isoquinolinium derivatives, which were converted to 2,6-diaryl-4-polyfluoroalkylpyridines, including those with the benzocrown-ether fragment. © 2014 Springer Science+Business Media New York.
KW - 1 3 3-trimethyl-3 4-dihydroisoquinolines
KW - 2 6-diaryl-4-poly-fluoroalkylpyridines
KW - 2-polyfluoroalkylchromones
KW - atropisomerism
KW - benzocrown ethers
KW - pyrido[2 1-a]isoquinolinium zwitterions
UR - http://www.scopus.com/inward/record.url?scp=84924253449&partnerID=8YFLogxK
UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000350877500012
U2 - 10.1007/s11172-014-0600-0
DO - 10.1007/s11172-014-0600-0
M3 - Article
AN - SCOPUS:84924253449
VL - 63
SP - 1337
EP - 1343
JO - Russian Chemical Bulletin
JF - Russian Chemical Bulletin
SN - 1066-5285
IS - 6
ER -
