Use of aldolases in the synthesis of non-carbohydrate natural products. Stereoselective synthesis of aspicilin C-3—C-9 fragment

1997 ◽  
Vol 75 (1) ◽  
pp. 68-73 ◽  
Author(s):  
Robert Chênevert ◽  
Michèle Lavoie ◽  
Mohammed Dasser

The C-3—C-9 main fragment of aspicilin was prepared via a fructose 1,6-diphosphate aldolase reaction. The same fragment was also synthesized by chemical transformation starting from D-arabinose. Key words: aldolase, aspicilin, arabinose, synthesis.




Author(s):  
Natalia M. Padial ◽  
Esther Roldan-Molina ◽  
Antonio Rosales ◽  
Míriam Álvarez-Corral ◽  
Ignacio Rodríguez-García ◽  
...  


2007 ◽  
Vol 79 (2) ◽  
pp. 163-172 ◽  
Author(s):  
Luiz C. Dias ◽  
Luciana G. de Oliveira ◽  
Paulo R. R. Meira

This paper describes the convergent and stereocontrolled asymmetric total synthesis of (+)-crocacins C and D, potent inhibitors of animal cell cultures and several yeasts and fungi, and (-)-callystatin A, a potent antitumor polyketide.



ChemInform ◽  
2009 ◽  
Vol 40 (15) ◽  
Author(s):  
Piotr Roszkowski ◽  
Stefan Czarnocki ◽  
Jan K. Maurin ◽  
Aleksandra Siwicka ◽  
Anna Zawadzka ◽  
...  


2016 ◽  
Vol 2016 (27) ◽  
pp. 4674-4695 ◽  
Author(s):  
Ángel M. Montaña ◽  
Albert Corominas ◽  
Juan F. Chesa ◽  
Francisca García ◽  
Mercè Font-Bardia


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