Synthetic Studies on a Marine Natural Product, Palmerolide A (I): Synthesis of C1—C9 and C15—C21 Fragments.

ChemInform ◽  
2007 ◽  
Vol 38 (43) ◽  
Author(s):  
Krishna P. Kaliappan ◽  
Parthasarathy Gowrisankar
Synlett ◽  
2007 ◽  
Vol 2007 (19) ◽  
pp. 2983-2986
Author(s):  
Christophe Meyer ◽  
Janine Cossy ◽  
Guillaume Cantagrel

Synlett ◽  
2007 ◽  
Vol 2007 (10) ◽  
pp. 1537-1540 ◽  
Author(s):  
Krishna Kaliappan ◽  
Parthasarathy Gowrisankar

2016 ◽  
Vol 14 (28) ◽  
pp. 6769-6779 ◽  
Author(s):  
Sudhakar Athe ◽  
Ashish Sharma ◽  
Kanakaraju Marumudi ◽  
Subhash Ghosh

Synthesis of the fully functionalized macrolactone core of the highly cytotoxic marine natural product callyspongiolide has been achievedviaaZ-selective intramolecular H–W–E reaction and allylic alkylation of an activatedZ-allylic alcoholviaan SN2′ fashion as key steps.


Author(s):  
Ardalan A. Nabi ◽  
Lydia M. Scott ◽  
Daniel P. Furkert ◽  
Jonathan Sperry

The rare benzoxazepine ring in the alkaloid inducamide C is unstable and prone to rearrangement, indicating that structural revision of the natural product may be necessary.


Planta Medica ◽  
2013 ◽  
Vol 79 (10) ◽  
Author(s):  
M Albadry ◽  
Y Zou ◽  
Y Takahashi ◽  
A Waters ◽  
M Hossein ◽  
...  

Planta Medica ◽  
2008 ◽  
Vol 74 (03) ◽  
Author(s):  
JJ Bowling ◽  
PR Daga ◽  
S Odde ◽  
SA Ahmed ◽  
MK Mesbah ◽  
...  

Author(s):  
Shivaji Narayan Khadake ◽  
Shaik Karamathulla ◽  
Tapan Kumar Jena ◽  
Mohan Monisha ◽  
Nikhil Kumar Tuti ◽  
...  

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