The study of using intramolecular nucleophile substitution to synthesis the furan ring,and the synthesis of(-)-Pachastrissamine
碩士 === 國立中央大學 === 化學研究所 === 100 === (-)-Pachastrissamine was synthesized using (3R,4R)-hexa- 1,5-diene-3,4-diol 48 as the starting material. We applied Sharpless epoxidation to create the third chirality center. Tert-Butyldimethylsilyl chloride was used to protect the remaing two hydroxyl groups. Li...
Main Authors: | Cheng-Wei Lin, 林振暐 |
---|---|
Other Authors: | Duen-Ren Hou |
Format: | Others |
Language: | zh-TW |
Published: |
2012
|
Online Access: | http://ndltd.ncl.edu.tw/handle/03971992450565539484 |
Similar Items
-
Synthesis and Biological Evaluation of Carbocyclic Analogues of Pachastrissamine
by: Yongseok Kwon, et al.
Published: (2015-02-01) -
Total synthesis of (-)-Pachastrissamine and it''s 4-epimer
by: Shin-wei Liu, et al.
Published: (2010) -
Concise synthesis of truncated pachastrissamine (jaspine B) and its enantiomer
by: S. Chandrasekhar, et al.
Published: (2006-06-01) -
Synthesis of 1H-quinazoline-4-ones using intramolecular aromatic nucleophilic substitution
by: W. Russell Bowman, et al.
Published: (2003-10-01) -
An investigation of the preparation of heterocyclic ring systems via intramolecular nucleophilic aromatic substitution
by: Smith, Philip Henry Gaunt
Published: (1985)