An efficient, short and, a convenient asymmetric total synthesis of filamentous fungi related resorcylic acid lactones 7-epi-zeaenol (2) and zeaenol (1) have been achieved in 7 and 9 linear steps with the high overall yield of 32% and 21% respectively, from the known intermediate 13. Mitsunobu inversion, De Brabander’s protocol for macrolactonisation, Heck cross-coupling, diastereoselective alkyne aldehyde coupling and Ohira–Bestmann alkynylation are the key reactions
The first asymmetric total syntheses of sesquiterpene lactones (+)-eudesmadiene-12,6-olide (<b>1</b>...
The aim of this study was to obtain new unsaturated lactones by chemical synthesis and their microbi...
Total syntheses of the macrolides (R)-(+)-ricinelaidic acid lactone (6) and (−)-gloeosporone (7), a ...
The natural products cochliomycin A (1) and cochliomycin B (2), two resorcylic acid lactones obtaine...
The first asymmetric total synthesis of Aspinolide B (1), a new 10-membered lactone discovered by ch...
The first asymmetric total synthesis of Aspinolide B (1), a new 10-membered lactone discovered by ch...
The natural products cochliomycin A (<b>1</b>) and cochliomycin B (<b>2</b>), two resorcylic acid la...
<p>The total synthesis of 14-membered resorcylic acid macrolide, β-zearalenol, was accomplished star...
In reporting a total synthesis of erythromycin (la) we described in the preceding paper1 the synthes...
The thesis describes the synthesis and application of various alkynones derived from the bis-Weinreb...
The total synthesis of citrafungin A (i),1 the determination of the absolute stereochemistry2 of CJ-...
A total, stereoselective synthesis of the cytotoxic macrolide aspergillide B has been performed. A c...
ω-Alkynal ester 3, prepared from (S)-propylene oxide 4, yields the macrocyclic (6R)-allylic alcohol ...
Resorcylic acid lactones (RALs) are biologically active polyketide natural products with typically a...
The total synthesis of the polyhydroxylated macrolide (+)-aspicilin 5 is described using as a key st...
The first asymmetric total syntheses of sesquiterpene lactones (+)-eudesmadiene-12,6-olide (<b>1</b>...
The aim of this study was to obtain new unsaturated lactones by chemical synthesis and their microbi...
Total syntheses of the macrolides (R)-(+)-ricinelaidic acid lactone (6) and (−)-gloeosporone (7), a ...
The natural products cochliomycin A (1) and cochliomycin B (2), two resorcylic acid lactones obtaine...
The first asymmetric total synthesis of Aspinolide B (1), a new 10-membered lactone discovered by ch...
The first asymmetric total synthesis of Aspinolide B (1), a new 10-membered lactone discovered by ch...
The natural products cochliomycin A (<b>1</b>) and cochliomycin B (<b>2</b>), two resorcylic acid la...
<p>The total synthesis of 14-membered resorcylic acid macrolide, β-zearalenol, was accomplished star...
In reporting a total synthesis of erythromycin (la) we described in the preceding paper1 the synthes...
The thesis describes the synthesis and application of various alkynones derived from the bis-Weinreb...
The total synthesis of citrafungin A (i),1 the determination of the absolute stereochemistry2 of CJ-...
A total, stereoselective synthesis of the cytotoxic macrolide aspergillide B has been performed. A c...
ω-Alkynal ester 3, prepared from (S)-propylene oxide 4, yields the macrocyclic (6R)-allylic alcohol ...
Resorcylic acid lactones (RALs) are biologically active polyketide natural products with typically a...
The total synthesis of the polyhydroxylated macrolide (+)-aspicilin 5 is described using as a key st...
The first asymmetric total syntheses of sesquiterpene lactones (+)-eudesmadiene-12,6-olide (<b>1</b>...
The aim of this study was to obtain new unsaturated lactones by chemical synthesis and their microbi...
Total syntheses of the macrolides (R)-(+)-ricinelaidic acid lactone (6) and (−)-gloeosporone (7), a ...