ChemInform Abstract: Total Synthesis and Absolute Stereochemistry of Novel Biologically Active Marine Natural Products of Halenaquinol Family: Theoretical Studies of CD Spectra

ChemInform ◽  
2010 ◽  
Vol 27 (15) ◽  
pp. no-no
Author(s):  
N. HARADA ◽  
T. SUGIOKA
2003 ◽  
Vol 75 (2-3) ◽  
pp. 209-221 ◽  
Author(s):  
S. Hanessian ◽  
Roberto Margarita ◽  
Adrian Hall ◽  
Shawn Johnstone ◽  
M. Tremblay ◽  
...  

The total synthesis of dysinosin A, a novel member of the aeruginosin group of marine natural products is discussed. The stereocontrolled synthesis also confirms the proposed structure and absolute stereochemistry of the natural product.


2017 ◽  
Vol 15 (22) ◽  
pp. 4842-4850 ◽  
Author(s):  
Subhendu Das ◽  
Rajib Kumar Goswami

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 ◽  
2009 ◽  
Vol 78 (1) ◽  
pp. 1 ◽  
Author(s):  
Daisuke Uemura ◽  
Kazuhiko Nakamura ◽  
Makoto Kitamura

1982 ◽  
Vol 13 (13) ◽  
Author(s):  
A. G. GONZALEZ ◽  
J. D. MARTIN ◽  
C. PEREZ ◽  
M. A. RAMIREZ ◽  
F. RAVELO

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