Unknown

Dataset Information

0

An efficient route to N-alkylated 3,4-dihydroisoquinolinones with substituents at the 3-position.


ABSTRACT: A facile synthetic procedure for the production of N-alkylated 3,4-dihydroisoquinolinone derivatives is described. The desired products were obtained by N-alkylation of 3,3'-dimethyl-3,4-dihydroisoquinoline derivatives followed by oxidation of the resulting iminium salts. Reaction conditions for both steps were very mild and the desired cyclization products could be obtained in good yield. This strategy allows the generation of N-substituted 3,4-dihydroisoquinolinone derivatives with substituents at the 3-position.

SUBMITTER: Tazawa A 

PROVIDER: S-EPMC9078240 | biostudies-literature | 2018 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

An efficient route to <i>N</i>-alkylated 3,4-dihydroisoquinolinones with substituents at the 3-position.

Tazawa Aoi A   Ando Junki J   Ishizawa Kohei K   Azumaya Isao I   Hikawa Hidemasa H   Tanaka Minoru M  

RSC advances 20180207 11


A facile synthetic procedure for the production of <i>N</i>-alkylated 3,4-dihydroisoquinolinone derivatives is described. The desired products were obtained by <i>N</i>-alkylation of 3,3'-dimethyl-3,4-dihydroisoquinoline derivatives followed by oxidation of the resulting iminium salts. Reaction conditions for both steps were very mild and the desired cyclization products could be obtained in good yield. This strategy allows the generation of <i>N</i>-substituted 3,4-dihydroisoquinolinone derivat  ...[more]

Similar Datasets

| S-EPMC6071743 | biostudies-literature
| S-EPMC6241324 | biostudies-literature
| S-EPMC4660899 | biostudies-literature
| S-EPMC2811074 | biostudies-literature
| S-EPMC3281748 | biostudies-literature
| S-EPMC9658173 | biostudies-literature
| S-EPMC5974014 | biostudies-literature
| S-EPMC8025870 | biostudies-literature
| S-EPMC1450324 | biostudies-literature
| S-EPMC7497243 | biostudies-literature