Central Asia and the Caucasus.
CA and CC Press AB.
Vol. 17.
2016.
P. 70-79
Domino reactions of 1-substituted N-(cyanomethyl)isoquinolinium salts with salicylic aldehydes
[Figure not available: see fulltext.] Transformations of N-cyanomethyl-substituted 1-methyl- and 1-phenylisoquinolinium salts were studied in the presence of various o-hydroxybenzaldehydes, leading to the formation of substituted chromeno[2',3':4,5]imidazo[2,1-a]isoquinolines. 1,8-Diazabicyclo- [5.4.0]undec-7-ene was shown to be a superior base in this reaction compared to sodium carbonate. © 2016, Springer Science+Business Media New York.
Authors
Voskressensky L.G.
1
,
Sokolova E.A.
1
,
Festa A.A.
1
,
Enina D.A.
1
,
Aksenov A.V.2
,
Varlamov A.V.
1
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
6
Language
English
Pages
415-420
Status
Published
Link
Volume
52
Year
2016
Organizations
- 1 Peoples’ Friendship University of Russia, 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation
- 2 North-Caucasus Federal University, 1 Pushkina St, Stavropol, 350009, Russian Federation
Keywords
domino reaction; isoquinoline; quaternary salts; salicylic aldehyde
Date of creation
19.10.2018
Date of change
19.10.2018
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Other records
Eurasian Soil Science.
Vol. 49.
2016.
P. 632-639