Journal of Heterocyclic Chemistry p. 767 - 771 (2000)
Update date:2022-08-03
Topics:
Prat
Bureau
Daveu
Levacher
Dupas
Queguiner
Bourguignon
The synthesis of N-methyl-4-pyridyl-1,2,3,4-tetrahydroisoquinolines (6a,b,c) was achieved via a Pictet-Spengler cyclization of an activated amino group derivatized in a carbamate form. The obtained compounds have been designed as potential serotonin analo
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Doi:10.1021/jo00367a019
(1986)Doi:10.1071/CH99134
(2000)Doi:10.1139/v71-124
(1971)Doi:10.1039/b005353h
(2000)Doi:10.3390/ijms22041907
(2021)Doi:10.1039/b004782L
(2000)
