scholarly journals Stereoselective synthesis of the C79–C97 fragment of symbiodinolide

2013 ◽  
Vol 9 ◽  
pp. 1931-1935 ◽  
Author(s):  
Hiroyoshi Takamura ◽  
Takayuki Fujiwara ◽  
Isao Kadota ◽  
Daisuke Uemura

Symbiodinolide is a polyol marine natural product with a molecular weight of 2860. Herein, a streamlined synthesis of the C79–C97 fragment of symbiodinolide is described. In the synthetic route, a spiroacetalization, a Julia–Kocienski olefination, and a Sharpless asymmetric dihydroxylation were utilized as the key transformations.

1996 ◽  
Vol 37 (39) ◽  
pp. 7071-7074 ◽  
Author(s):  
Wei-guo Gao ◽  
Kazuhiko Sakaguchi ◽  
Sachihiko Isoe ◽  
Yasufumi Ohfune

Synlett ◽  
2018 ◽  
Vol 30 (02) ◽  
pp. 185-188 ◽  
Author(s):  
Stéphanie Ballereau ◽  
Heba Alnazer ◽  
Tessa Castellan ◽  
Yahya Salma ◽  
Yves Génisson

A short enantioselective synthetic route to the cytotoxic marine natural product jaspine B has been developed. A chiral non-racemic primary α-allenol, obtained from pentadecanal, gave access to an enantioenriched 2-tetradecyl-2,5-dihydrofuran as key intermediate. A stereodivergent functionalization of this dihydrofuran allowed access in a few steps to jaspine B and its 4-epimer.


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 ◽  
...  

2013 ◽  
Vol 13 (10) ◽  
pp. 1514-1530 ◽  
Author(s):  
Srinivas Tekkam ◽  
Mohammad Alam ◽  
Matthew Just ◽  
Steven Berry ◽  
Joseph Johnson ◽  
...  

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

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