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Molecules 1997, 2(8), M25; doi:10.3390/M25

1,2,3,4-Tetrahydroisoquinoline from Acid Catalysed Cyclisation of N,N'-Dibenzylethylenediamine

Faculty of Science, Northern Territory University, Casuarina, Darwin, Northern, Territory, Australia 9090
Received: 8 August 1997 / Published: 12 August 1997
(This article belongs to the Section Molbank Section of Molecules, 1997-2001)
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1,2,3,4-Tetrahydroisoquinolines have been traditionally prepared by the Bischler- Napieralski, Pictet-Gams, Pictet-Spengler, Pomeranz-Fritsch reactions and various Friedel- Crafts cyclization procedures of N-(haloalkyl)aryl derivatives [1].[...] View Full-Text
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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MDPI and ACS Style

Peerzada, N. 1,2,3,4-Tetrahydroisoquinoline from Acid Catalysed Cyclisation of N,N'-Dibenzylethylenediamine. Molecules 1997, 2, M25.

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