Synthesis of decaline analogues of isovelleral
Research output: Contribution to journal › Article
Decaline analogues of the bioactive fungal sesquiterpene (+)-isovelleral (1a), retaining the bicyclo[4,1,0]hept-2-en-1,2-dicarbaldehyde system, were prepared, and their cytotoxic and antimicrobial activities were compared with those of the natural product. While the two isomers (+/-)-2 and (+/-)-3 were as active as isovelleral (1a), the isomer (+/-)-4 was approximately 10 times less potent.
|Research areas and keywords||
Subject classification (UKÄ) – MANDATORY
|Journal||Zeitschrift fuer Naturforschung. Section B: A Journal of Chemical Sciences|
|Publication status||Published - 2005|
The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Organic chemistry (S/LTH) (011001240)