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., 2005, том 15, выпуск 3,страницы 125

Эта публикация цитируется в 4 статьях

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. Shklyaev^a, V. A. Glushkov^a, M. A. El'tsov^a, Yu. V. Gatilov^a, I. Yu. Bagryanskaya^b, A. G. Tolstikov^a

^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

Аннотация: 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.

Язык публикации: английский

DOI: 10.1070/MC2005v015n03ABEH001948