ChemInform Abstract: SYNTHETIC STUDIES OF MARINE NATURAL PRODUCTS. VIII. TOTAL SYNTHESIS OF (.+-.)-APLYSIN-20

1985 ◽  
Vol 16 (10) ◽  
Author(s):  
A. MURAI ◽  
A. ABIKO ◽  
T. MASAMUNE
Keyword(s):  
Natural Products ◽  
Total Synthesis ◽  
Marine Natural Products ◽  
Synthetic Studies

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

scholarly journals Total synthesis and structural elucidation of natural products: (–)-Delactonmycin, (+)-plumerinine, and (–)-parvistemoamide

2005 ◽  
Vol 77 (7) ◽  
pp. 1153-1160 ◽  
Author(s):  
Ronaldo A. Pilli ◽  
Ivan R. Corrêa ◽  
Adriano O. Maldaner ◽  
Giovanni B. Rosso
Keyword(s):  
Natural Products ◽  
Total Synthesis ◽  
Inhibitory Activity ◽  
Structural Elucidation ◽  
Relative Configuration ◽  
Synthetic Studies ◽  
Hiv 1 ◽  
Rev Protein

Synthetic studies that established the relative configuration of (–)-delactonmycin, a polyketide with inhibitory activity against HIV-1 Rev protein, and our efforts toward the structural elucidation of the alkaloids (+)-plumerinine, isolated from P. rubra, and (–)-parvistemoamide, isolated from S. parviflora, are discussed.

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