Studies towards the synthesis of the northern polyene of viridenomycin and synthesis of Z-double bond analogues.
Org Biomol Chem
; 9(6): 1876-86, 2011 Mar 21.
Article
em En
| MEDLINE
| ID: mdl-21283899
ABSTRACT
Viridenomycin is a structurally challenging, potentially biologically valuable molecule which has yet to succumb to total synthesis. Its instability, perhaps particularly associated with the northern polyene may contribute to the difficulties of piecing this molecule together. The synthesis of northern polyene models, including potentially stabilised analogues incorporating benzene rings as Z-alkene replacements, have been prepared using an efficient series of cross-coupling reactions. The resulting polyenes and polyene surrogates have been converted into tetraene ester and amide models of the viridenomycin system. These analogues have sufficient stability compared with the unsubstituted northern polyene analogue to be viable for future developing a strategy for the construction of viridenomycin and analogues.
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Base de dados:
MEDLINE
Assunto principal:
Polienos
Idioma:
En
Ano de publicação:
2011
Tipo de documento:
Article