Sesquiterpenes have been a rich source of bioactive compounds and have inspired innovative methodological developments. Herein we report a rapid and scalable synthesis of a substrate for a 4+3 cycloaddition in order to access the cis-fused bicyclic system of the guaianes. We further show diverse and efficient functionalizations of the bicyclic system. The relative stereochemistry was assigned based on the crystal structure of a key product
A domino silver(I)-promoted electrocyclic 2π-disrotatory electrocyclic ring-opening/intramolecular ...
A stereocontrolled approach to the cis-decalin framework of clerodane diterpenes and biologically ac...
The [2+2] cycloaddition of dichloroketene and monosubstituted cycloheptatrienes, followed by ring ex...
International audienceA promising synthetic route towards bioactive guaianolide sesquiterpene lacton...
Guaianolides, known as biologically important hydroazulenic sesquiterpene lactones, have so far only...
By using a gallium(III) triflate catalyzed intramolecular (4+3) cycloaddition, a few functionalized ...
Natural selection: An acyclic chain containing an ene-yne-ene motif, in analogy to farnesyl diphosph...
An efficient, 8-step synthesis of (+)-∝-cyperone 168 from (-)-∝-santonin 107 is described. Epimeriza...
Sesquiterpene skeletal complexity in nature originates from the enzyme-catalyzed ionization of (tran...
(−)-Isoguaiene was prepared from (S)-citronellal in only 9–10 steps with good overall yields. Either...
Guaianolides constitute a large and diverse group of biologically active sesquiterpenes. Guaianolide...
The first total synthesis of (−)-dendroside C aglycon, consisting of a 1,4,5-tri-<i>cis</i>-guaiane ...
A new and flexible approach toward the synthesis of 6,12-guaianolide anticancer drugs such as trilob...
Combined experimental and computational efforts have demonstrated the utility of divergent photocycl...
A palladium catalyzed Barbier allylation/translactonization cascade reaction was established for the...
A domino silver(I)-promoted electrocyclic 2π-disrotatory electrocyclic ring-opening/intramolecular ...
A stereocontrolled approach to the cis-decalin framework of clerodane diterpenes and biologically ac...
The [2+2] cycloaddition of dichloroketene and monosubstituted cycloheptatrienes, followed by ring ex...
International audienceA promising synthetic route towards bioactive guaianolide sesquiterpene lacton...
Guaianolides, known as biologically important hydroazulenic sesquiterpene lactones, have so far only...
By using a gallium(III) triflate catalyzed intramolecular (4+3) cycloaddition, a few functionalized ...
Natural selection: An acyclic chain containing an ene-yne-ene motif, in analogy to farnesyl diphosph...
An efficient, 8-step synthesis of (+)-∝-cyperone 168 from (-)-∝-santonin 107 is described. Epimeriza...
Sesquiterpene skeletal complexity in nature originates from the enzyme-catalyzed ionization of (tran...
(−)-Isoguaiene was prepared from (S)-citronellal in only 9–10 steps with good overall yields. Either...
Guaianolides constitute a large and diverse group of biologically active sesquiterpenes. Guaianolide...
The first total synthesis of (−)-dendroside C aglycon, consisting of a 1,4,5-tri-<i>cis</i>-guaiane ...
A new and flexible approach toward the synthesis of 6,12-guaianolide anticancer drugs such as trilob...
Combined experimental and computational efforts have demonstrated the utility of divergent photocycl...
A palladium catalyzed Barbier allylation/translactonization cascade reaction was established for the...
A domino silver(I)-promoted electrocyclic 2π-disrotatory electrocyclic ring-opening/intramolecular ...
A stereocontrolled approach to the cis-decalin framework of clerodane diterpenes and biologically ac...
The [2+2] cycloaddition of dichloroketene and monosubstituted cycloheptatrienes, followed by ring ex...