Synthetic studies directed toward naturally occurring tetramic acids. 3. Synthesis of (-)-methyl ydiginate and the tetramic acid subunit for streptolydigin

1987 ◽  
Vol 52 (3) ◽  
pp. 469-472 ◽  
Author(s):  
Robert K. Boeckman ◽  
Joan C. Potenza ◽  
Eric J. Enholm
1992 ◽  
Vol 40 (10) ◽  
pp. 2614-2619 ◽  
Author(s):  
Hisashi ISHII ◽  
Tsutomu ISHIKAWA ◽  
Hisaya WADA ◽  
Hidetoshi MIYAZAKI ◽  
Yasuko KANEKO ◽  
...  

2015 ◽  
Vol 13 (28) ◽  
pp. 7795-7802 ◽  
Author(s):  
Zhuo Shang ◽  
Li Li ◽  
Breno P. Espósito ◽  
Angela A. Salim ◽  
Zeinab G. Khalil ◽  
...  
Keyword(s):  

Marine-derived fungus Chaunopycnis sp. yielded the tetramic acid F-14329 (1) and new analogues, chaunolidines A–C (2–4), together with the new pyridinone chaunolidone A (5), and pyridoxatin (6).


Author(s):  
Jo�l Poncet ◽  
Patrick Jouin ◽  
Bertrand Castro ◽  
Louisette Nicolas ◽  
Mohamed Boutar ◽  
...  
Keyword(s):  

2015 ◽  
Vol 13 (42) ◽  
pp. 10527-10531 ◽  
Author(s):  
A. R. Healy ◽  
N. J. Westwood

A successful late-stage Diels–Alder cyclisation in the synthesis of JBIR-22 highlights it as a viable biosynthetic event.


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