The synthesis of a stereoisomer library of 16 murisolins in individual pure form by fluorous mixture synthesis is reported. Four stereoisomeric precursors are tagged with different fluorous tags, and the resulting mixture is taken through the synthesis with four splits and late stage demixing and detagging to give all 16 products. These products exhibit only six different sets of NMR spectra, but all can be differentiated by chiral HPLC. The structure of murisolin is confirmed, but the structures of murisolin A and 16,19-cis-murisolin may never be known with certainty because insufficient data were collected on natural samples to differentiate each of them from one other isomer.\ud \u
All 16 stereoisomers of the sex pheromone of pine sawfly (3,7,11-trimethylundecanol propanoate ester...
All four diastereomers of a typical saturated oligoisoprenoid, 4,8,12-trimethylnonadecanol, are made...
The principles of the oligoethylene glycol (OEG) mixture synthesis are illustrated with the synthesi...
The synthesis of a stereoisomer library of 16 murisolins in individual pure form by fluorous mixture...
Total syntheses of two 16-member libraries of murisolin isomers are reported. In the first library, ...
Total syntheses of two 16-member libraries of murisolin isomers are reported. In the first library, ...
Sixteen individual stereoisomers of murisolin are synthesized together and isolated in pure form wit...
Characterizing a stereoisomer library of 28 of the 64 possible isomers of the acetogenin murisolin, ...
Characterizing a stereoisomer library of 28 of the 64 possible isomers of the acetogenin murisolin, ...
Chapter 1 of this thesis describes two new strategies for the solution phase mixture synthesis: OEG-...
(Chemical Equation Presented) Two tags are better than one: Sixteen individual stereoisomers of muri...
Fluorous mixture synthesis minimizes the effort to synthesize small-molecule libraries by labelling ...
All four diastereomers of a typical saturated oligoisoprenoid, 4,8,12-trimethylnonadecanol, are made...
Fluorous mixture synthesis minimizes the effort to synthesize small-molecule libraries by labelling ...
Transannular <i>O</i>-heterocyclization is applied as a key step in a total synthesis. This highly s...
All 16 stereoisomers of the sex pheromone of pine sawfly (3,7,11-trimethylundecanol propanoate ester...
All four diastereomers of a typical saturated oligoisoprenoid, 4,8,12-trimethylnonadecanol, are made...
The principles of the oligoethylene glycol (OEG) mixture synthesis are illustrated with the synthesi...
The synthesis of a stereoisomer library of 16 murisolins in individual pure form by fluorous mixture...
Total syntheses of two 16-member libraries of murisolin isomers are reported. In the first library, ...
Total syntheses of two 16-member libraries of murisolin isomers are reported. In the first library, ...
Sixteen individual stereoisomers of murisolin are synthesized together and isolated in pure form wit...
Characterizing a stereoisomer library of 28 of the 64 possible isomers of the acetogenin murisolin, ...
Characterizing a stereoisomer library of 28 of the 64 possible isomers of the acetogenin murisolin, ...
Chapter 1 of this thesis describes two new strategies for the solution phase mixture synthesis: OEG-...
(Chemical Equation Presented) Two tags are better than one: Sixteen individual stereoisomers of muri...
Fluorous mixture synthesis minimizes the effort to synthesize small-molecule libraries by labelling ...
All four diastereomers of a typical saturated oligoisoprenoid, 4,8,12-trimethylnonadecanol, are made...
Fluorous mixture synthesis minimizes the effort to synthesize small-molecule libraries by labelling ...
Transannular <i>O</i>-heterocyclization is applied as a key step in a total synthesis. This highly s...
All 16 stereoisomers of the sex pheromone of pine sawfly (3,7,11-trimethylundecanol propanoate ester...
All four diastereomers of a typical saturated oligoisoprenoid, 4,8,12-trimethylnonadecanol, are made...
The principles of the oligoethylene glycol (OEG) mixture synthesis are illustrated with the synthesi...