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Mendeleev Communications, 2005, Volume 15, Issue 3, Pages 125–127
DOI: https://doi.org/10.1070/MC2005v015n03ABEH001948
(Mi mendc3708)
 

This article is cited in 4 scientific papers (total in 4 papers)

Synthesis of regioisomeric (S)-(+)-3,3,4-trimethyl-8-methoxy-3,4-dihydrobenzo[h]-isoquinolin-1(2H)-one and (S)-(+)-1,2,2-trimethyl-8-methoxy-1,2-dihydrobenzo[f]-isoquinolin-4(3H)-one by the Ritter reaction

Yu. V. Shklyaeva, V. A. Glushkova, M. A. El'tsova, Yu. V. Gatilova, I. Yu. Bagryanskayab, A. G. Tolstikova

a Institute of Technical Chemistry, Ural Branch of the Russian Academy of Sciences, Perm, Russian Federation
b N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
Full-text PDF (226 kB) Citations (4)
Abstract: The conservation of chirality at the α-position to the carbocationic centre of (S)-(−)-2-methyl-3-(6-methoxynaphth-2-yl)butan-2-ol and the formation of regioisomeric (S)-(+)-1,2,2-trimethyl-8-methoxy-1,2-dihydrobenzo[f]isoquinolin-4(3H)-one were found in the synthesis of (S)-(+)-3,3,4-trimethyl-8-methoxy-3,4-dihydrobenzo[h]isoquinolin-1(2H)-one by the Ritter reaction.
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Document Type: Article
Language: English


Citation: Yu. V. Shklyaev, V. A. Glushkov, M. A. El'tsov, Yu. V. Gatilov, I. Yu. Bagryanskaya, A. G. Tolstikov, “Synthesis of regioisomeric (S)-(+)-3,3,4-trimethyl-8-methoxy-3,4-dihydrobenzo[h]-isoquinolin-1(2H)-one and (S)-(+)-1,2,2-trimethyl-8-methoxy-1,2-dihydrobenzo[f]-isoquinolin-4(3H)-one by the Ritter reaction”, Mendeleev Commun., 15:3 (2005), 125–127
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  • https://www.mathnet.ru/eng/mendc/v15/i3/p125
  • This publication is cited in the following 4 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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