The enantiomeric form, 1R, of the structure (1S) assigned to the phytotoxic natural product phomentrioloxin has been synthesized in seven steps from the homochiral cis-1,2-dihydrocatechol 3. These studies reveal that the true structure of phomentrioloxi
A total synthesis of the fungal-derived natural prod-uct pestynol is reported via a convergent chemo...
Enantiospecific total synthesis of the phytoalexins, solavetivone, anhydro-β-rotunol, solanascone, a...
A total synthesis of the title natural product, 1, has been achieved using the cis-1,2-dihydrocatech...
The enantiomeric form, <b>1</b><i>R</i>, of the structure (<b>1</b><i>S</i>) assigned to the phytoto...
A series of 28 analogues of the phytotoxic geranylcyclohexentriol (−)-phomentrioloxin A (1) has been...
A series of 28 analogues of the phytotoxic geranylcyclohexentriol (−)-phomentrioloxin A (<b>1</b>) h...
The limitations of an alcohol dehydrogenase regarding the oxidative kinetic resolution of homoallyli...
A synthesis of (+)-gephyrotoxin 287C using (<i>S</i>)-phenylglycinol-derived tricyclic lactam <b>7</...
Different enzymatic and nonenzymatic approaches were tested and compared to afford enantiopure homoa...
Total syntheses of (+)-asperpentyn (<b>1</b>) and compound <i>ent</i>-<b>2</b>, the enantiomer of th...
A synthesis of (+)-gephyrotoxin 287C using, (S)-phenylglycinol-derived tricyclic lactam 7 as the sta...
Phomentrioloxin is a phytotoxic geranylcyclohexenetriol produced in liquid culture by Phomopsis sp. ...
A new phytotoxic geranylcyclohexenetriol, named phomentrioloxin, was isolated from the liquid cultur...
Synthesis of enantiomerically pure and biologically important molecules is one of the most challengi...
The enantiomerically pure cis-1,2-diol 2, which is obtained by microbial oxidation of naphthalene, h...
A total synthesis of the fungal-derived natural prod-uct pestynol is reported via a convergent chemo...
Enantiospecific total synthesis of the phytoalexins, solavetivone, anhydro-β-rotunol, solanascone, a...
A total synthesis of the title natural product, 1, has been achieved using the cis-1,2-dihydrocatech...
The enantiomeric form, <b>1</b><i>R</i>, of the structure (<b>1</b><i>S</i>) assigned to the phytoto...
A series of 28 analogues of the phytotoxic geranylcyclohexentriol (−)-phomentrioloxin A (1) has been...
A series of 28 analogues of the phytotoxic geranylcyclohexentriol (−)-phomentrioloxin A (<b>1</b>) h...
The limitations of an alcohol dehydrogenase regarding the oxidative kinetic resolution of homoallyli...
A synthesis of (+)-gephyrotoxin 287C using (<i>S</i>)-phenylglycinol-derived tricyclic lactam <b>7</...
Different enzymatic and nonenzymatic approaches were tested and compared to afford enantiopure homoa...
Total syntheses of (+)-asperpentyn (<b>1</b>) and compound <i>ent</i>-<b>2</b>, the enantiomer of th...
A synthesis of (+)-gephyrotoxin 287C using, (S)-phenylglycinol-derived tricyclic lactam 7 as the sta...
Phomentrioloxin is a phytotoxic geranylcyclohexenetriol produced in liquid culture by Phomopsis sp. ...
A new phytotoxic geranylcyclohexenetriol, named phomentrioloxin, was isolated from the liquid cultur...
Synthesis of enantiomerically pure and biologically important molecules is one of the most challengi...
The enantiomerically pure cis-1,2-diol 2, which is obtained by microbial oxidation of naphthalene, h...
A total synthesis of the fungal-derived natural prod-uct pestynol is reported via a convergent chemo...
Enantiospecific total synthesis of the phytoalexins, solavetivone, anhydro-β-rotunol, solanascone, a...
A total synthesis of the title natural product, 1, has been achieved using the cis-1,2-dihydrocatech...