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

碩士 === 國立中山大學 === 化學系研究所 === 88 === 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 carboli...

Full description

Bibliographic Details
Main Authors:	Shi-Ta Tsai, 蔡昕達
Other Authors:	Chih-Shone Lee
Format:	Others
Language:	zh-TW
Published:	1999
Online Access:	http://ndltd.ncl.edu.tw/handle/11576091249793199247

id	ndltd-TW-088NSYS5065001
record_format	oai_dc
spelling	ndltd-TW-088NSYS50650012016-07-08T04:22:56Z http://ndltd.ncl.edu.tw/handle/11576091249793199247 Part I Synthesis of Yohimbane AlkaloidsPart II Synthetic Study of 3-aminoisoquinolines 主題一：育亨賓鹼生物鹼之合成研究主題二：3-胺基異□□化合物之合成研究 Shi-Ta Tsai 蔡昕達碩士國立中山大學化學系研究所 88 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. Chih-Shone Lee 李志雄 1999 學位論文 ; thesis 101 zh-TW
collection	NDLTD
language	zh-TW
format	Others
sources	NDLTD
description	碩士 === 國立中山大學 === 化學系研究所 === 88 === 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.
author2	Chih-Shone Lee
author_facet	Chih-Shone Lee Shi-Ta Tsai 蔡昕達
author	Shi-Ta Tsai 蔡昕達
spellingShingle	Shi-Ta Tsai 蔡昕達 Part I Synthesis of Yohimbane AlkaloidsPart II Synthetic Study of 3-aminoisoquinolines
author_sort	Shi-Ta Tsai
title	Part I Synthesis of Yohimbane AlkaloidsPart II Synthetic Study of 3-aminoisoquinolines
title_short	Part I Synthesis of Yohimbane AlkaloidsPart II Synthetic Study of 3-aminoisoquinolines
title_full	Part I Synthesis of Yohimbane AlkaloidsPart II Synthetic Study of 3-aminoisoquinolines
title_fullStr	Part I Synthesis of Yohimbane AlkaloidsPart II Synthetic Study of 3-aminoisoquinolines
title_full_unstemmed	Part I Synthesis of Yohimbane AlkaloidsPart II Synthetic Study of 3-aminoisoquinolines
title_sort	part i synthesis of yohimbane alkaloidspart ii synthetic study of 3-aminoisoquinolines
publishDate	1999
url	http://ndltd.ncl.edu.tw/handle/11576091249793199247
work_keys_str_mv	AT shitatsai partisynthesisofyohimbanealkaloidspartiisyntheticstudyof3aminoisoquinolines AT càixīndá partisynthesisofyohimbanealkaloidspartiisyntheticstudyof3aminoisoquinolines AT shitatsai zhǔtíyīyùhēngbīnjiǎnshēngwùjiǎnzhīhéchéngyánjiūzhǔtíèr3ànjīyìhuàhéwùzhīhéchéngyánjiū AT càixīndá zhǔtíyīyùhēngbīnjiǎnshēngwùjiǎnzhīhéchéngyánjiūzhǔtíèr3ànjīyìhuàhéwùzhīhéchéngyánjiū
_version_	1718340713793454080

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

Similar Items