Study of Pd Catalyzed Cross Coupling Reactions toward Ailanthoidols and Sexipyridines
碩士 === 國立彰化師範大學 === 化學系 === 92 === Abstract: Ailanthoidol 1, which can be isolated from Chinese herbal medicine, is achieved in which the longest linear sequence is only six steps in 48% overall yield from commercially available 5-bromo-2-hydroxy-3- methoxybenzaldehyde 9. The key transformations i...
Main Authors: | Shun-Yu Lin, 林順裕 |
---|---|
Other Authors: | Yean-Jang Lee |
Format: | Others |
Language: | zh-TW |
Published: |
2004
|
Online Access: | http://ndltd.ncl.edu.tw/handle/49698795411889173489 |
Similar Items
-
Synthesis of Kynapcins and Sexipyridines
by: Chih-Lung Chen, et al.
Published: (2005) -
Synthesisi of demethylwedelolactone and derivatives and supermolecular sexipyridine's monomer
by: 張筱微
Published: (2007) -
Theoretical Study on Pd-catalyzed Cross-Coupling Reactions.
by: García Melchor, Maximiliano
Published: (2012) -
Pd-Catalyzed Cross-Coupling Reactions of Amides and Aryl Mesylates
by: Dooleweerdt, Karin, et al.
Published: (2012) -
Inhibitory effect of Ailanthoidol on TPA induced inflammation and tumor promotion
by: Yea-Huey, et al.