Asymmetric Total Synthesis of Complex Marine Natural Products

ChemInform ◽  
2006 ◽  
Vol 37 (26) ◽  
Author(s):  
Jorma Hassfeld ◽  
Markus Kalesse ◽  
Timo Stellfeld ◽  
Mathias Christmann
Keyword(s):  
Natural Products ◽  
Total Synthesis ◽  
Marine Natural Products ◽  
Asymmetric Total Synthesis

ChemInform Abstract: The Apratoxin Marine Natural Products: Isolation, Structure Determination, and Asymmetric Total Synthesis

ChemInform ◽  
2015 ◽  
Vol 46 (37) ◽  
pp. no-no
Author(s):  
Emily M. Tarsis ◽  
Ettore J. Rastelli ◽  
Sarah E. Wengryniuk ◽  
Don M. Coltart
Keyword(s):  
Natural Products ◽  
Total Synthesis ◽  
Structure Determination ◽  
Marine Natural Products ◽  
Asymmetric Total Synthesis

scholarly journals The apratoxin marine natural products: isolation, structure determination, and asymmetric total synthesis

Tetrahedron ◽  
2015 ◽  
Vol 71 (31) ◽  
pp. 5029-5044 ◽  
Author(s):  
Emily M. Tarsis ◽  
Ettore J. Rastelli ◽  
Sarah E. Wengryniuk ◽  
Don M. Coltart
Keyword(s):  
Natural Products ◽  
Total Synthesis ◽  
Structure Determination ◽  
Marine Natural Products ◽  
Asymmetric Total Synthesis

Total synthesis of marine natural products separacenes A and B

2017 ◽  
Vol 15 (22) ◽  
pp. 4842-4850 ◽  
Author(s):  
Subhendu Das ◽  
Rajib Kumar Goswami
Keyword(s):  
Natural Products ◽  
Total Synthesis ◽  
Marine Natural Products

Total synthesis of the potent antifungal agents bengazole C and E

2009 ◽  
Vol 74 (6) ◽  
pp. 887-900 ◽  
Author(s):  
Álvaro Enríquez-García ◽  
Steven V. Ley
Keyword(s):  
Natural Products ◽  
Antifungal Activity ◽  
Total Synthesis ◽  
Marine Natural Products ◽  
Antifungal Agents ◽  
Nitrile Oxide ◽  
Total Syntheses ◽  
Unique Structure

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.

ChemInform Abstract: MARINE NATURAL PRODUCTS FROM THE ATLANTIC ZONE. PART 27. TOTAL SYNTHESIS OF OBTUSENOL

1982 ◽  
Vol 13 (13) ◽  
Author(s):  
A. G. GONZALEZ ◽  
J. D. MARTIN ◽  
C. PEREZ ◽  
M. A. RAMIREZ ◽  
F. RAVELO
Keyword(s):  
Natural Products ◽  
Total Synthesis ◽  
Marine Natural Products
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