Return to search

Part I Synthesis of Yohimbane Alkaloids Part II Synthetic Study of 3-aminoisoquinolines

Part I Studies on methodology development of the syntheses of carboline derivatives using Bischler-Napieralski reaction and electror-eduction gave moderate yields. Carbolines were undergone Mannich reaction to give yohimbane alkaloids. We got oxidative carboline products using Bischler-Napieralski reaction. We got carbolines or dimmer by the reaction of electroreduction in different condition.
Part II Phenylacetamides using Bischler-Napieralski reaction conditions with acetonitrile as a solvent, gave the 3-amino-isoquinolines. Various amides and various nitriles were undergone Bischler-Napieralski reaction conditions to give 3-aminoiso-quinoline products.

Identiferoai:union.ndltd.org:NSYSU/oai:NSYSU:etd-0613100-144945
Date13 June 2000
CreatorsTsai, Shi-Ta
ContributorsChih-Shone Lee, none, none
PublisherNSYSU
Source SetsNSYSU Electronic Thesis and Dissertation Archive
LanguageCholon
Detected LanguageEnglish
Typetext
Formatapplication/pdf
Sourcehttp://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0613100-144945
Rightsnot_available, Copyright information available at source archive

Page generated in 0.0011 seconds