Rapid stereocontrolled assembly of the fully substituted C-aryl glycoside of kendomycin with a Prins cyclization: a formal synthesis

2006 ◽  
pp. 2388 ◽  
Author(s):  
Kevin B. Bahnck ◽  
Scott D. Rychnovsky
Synlett ◽  
2007 ◽  
Vol 2007 (13) ◽  
pp. 2049-2052 ◽  
Author(s):  
J. Yadav ◽  
M. Reddy ◽  
P. Rao ◽  
A. Prasad

ChemInform ◽  
2008 ◽  
Vol 39 (1) ◽  
Author(s):  
J. S. Yadav ◽  
M. Sridhar Reddy ◽  
P. Purushothama Rao ◽  
A. R. Prasad

2003 ◽  
Vol 75 (1) ◽  
pp. 63-70 ◽  
Author(s):  
S. F. Martin

A unified approach for the synthesis of the four major groups of C-aryl glycosides has been developed. The strategy incorporates two integrated approaches, the first of which features the [4+2] cycloaddition of a glycosyl furan with a substituted benzyne followed by the acid-catalyzed opening of the resultant adduct. The second route involves the sequential palladium-catalyzed opening of a benzyne-furan cycloadduct with an iodo glycal followed by oxidation of the resultant dihydronaphthol ring and reduction of the glycal moiety. The utility of this strategy has been established by a concise formal synthesis of the C-aryl glycoside antibiotic galtamycinone.


2007 ◽  
pp. 939 ◽  
Author(s):  
Kok-Ping Chan ◽  
Yvonne Hui Ling ◽  
Teck-Peng Loh

Synthesis ◽  
2008 ◽  
Vol 2008 (24) ◽  
pp. 3945-3950 ◽  
Author(s):  
J. Yadav ◽  
Hissana Ather ◽  
K. Gayathri ◽  
N. Rao ◽  
A. Prasad

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