scholarly journals Total Synthesis of (−)-Mitrephorone A Enabled by Stereoselective Nitrile Oxide Cycloaddition and Tetrasubstituted Olefin Synthesis

2020 ◽  
Vol 142 (41) ◽  
pp. 17802-17809 ◽  
Author(s):  
Michael Schneider ◽  
Matthieu J. R. Richter ◽  
Erick M. Carreira
2009 ◽  
Vol 74 (6) ◽  
pp. 887-900 ◽  
Author(s):  
Álvaro Enríquez-García ◽  
Steven V. Ley

The bengazoles are marine natural products with unique structure, containing two oxazole rings flanking a single carbon. They show very potent antifungal activity. The total syntheses of bengazole C and E are described following a convergent route which involves diastereoselective cycloaddition of an appropriately substituted nitrile oxide with a butane-1,2-diacetal-protected alkenediol as the key step.


Heterocycles ◽  
1993 ◽  
Vol 36 (2) ◽  
pp. 345 ◽  
Author(s):  
Kozo Shishido ◽  
Koji Umimoto ◽  
Takeshi Takata ◽  
Osamu Irie ◽  
Masayuki Shibuya

2017 ◽  
Vol 19 (21) ◽  
pp. 6004-6007 ◽  
Author(s):  
Hyeonjeong Choe ◽  
Hyukjoon Cho ◽  
Hyun-Jeong Ko ◽  
Jongkook Lee

2016 ◽  
Vol 81 (6) ◽  
pp. 2612-2617 ◽  
Author(s):  
Hyeonjeong Choe ◽  
Thuy Trang Pham ◽  
Joo Yun Lee ◽  
Muhammad Latif ◽  
Haeil Park ◽  
...  

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