A total synthesis of the marine sponge meroterpenoid (+)-aureol has been achieved in 12 steps (6% overall yield) from (+)-sclareolide. Key steps of the synthesis include a biosynthetically inspired sequence of 1,2-hydride and methyl shifts, and a biomimetic cycloetherification reaction
Synthetic efforts towards various meroterpenoid natural products based on biosynthetic speculation w...
International audienceThis account reports a program of synthesis of aureothin from genesis to concl...
Here, we report a formal synthesis of the marine cytotoxic meroterpenoid actinoranone. Key steps inc...
A total synthesis of the marine sponge meroterpenoid (+)-aureol has been achieved in 12 steps (6% ov...
There is a longstanding interest in the total synthesis of meroterpenoid natural products. These sec...
Marine meroterpenoids have attracted a great deal of attention from synthetic research groups due to...
The marine sponge Aka coralliphaga is a rich source of biologically active and structurally interest...
A bioinspired and sustainable procedure for the straightforward synthesis of (±)-aureol has been ach...
A 12-step total synthesis of the natural product dysiherbol A, a strongly anti-inflammatory and anti...
Conspectus Natural products are biosynthesized from a limited pool of starting materials via pathway...
Complex architectures of marine terpenoids and vast assortments of their scaffolds have served as a ...
The first total synthesis of five austalide natural products, (±)-17S-dihydroaustalide K, (±)-austal...
A total synthesis of the marine sponge metabolite (-)-hyrtiosal along with its enantiomer (+)-hyrtio...
Heterogeneity of meroterpenoids arising from their dual biosynthetic origins is constantly provoking...
The divergent total synthesis strategy can be successfully applied to the preparation of families of...
Synthetic efforts towards various meroterpenoid natural products based on biosynthetic speculation w...
International audienceThis account reports a program of synthesis of aureothin from genesis to concl...
Here, we report a formal synthesis of the marine cytotoxic meroterpenoid actinoranone. Key steps inc...
A total synthesis of the marine sponge meroterpenoid (+)-aureol has been achieved in 12 steps (6% ov...
There is a longstanding interest in the total synthesis of meroterpenoid natural products. These sec...
Marine meroterpenoids have attracted a great deal of attention from synthetic research groups due to...
The marine sponge Aka coralliphaga is a rich source of biologically active and structurally interest...
A bioinspired and sustainable procedure for the straightforward synthesis of (±)-aureol has been ach...
A 12-step total synthesis of the natural product dysiherbol A, a strongly anti-inflammatory and anti...
Conspectus Natural products are biosynthesized from a limited pool of starting materials via pathway...
Complex architectures of marine terpenoids and vast assortments of their scaffolds have served as a ...
The first total synthesis of five austalide natural products, (±)-17S-dihydroaustalide K, (±)-austal...
A total synthesis of the marine sponge metabolite (-)-hyrtiosal along with its enantiomer (+)-hyrtio...
Heterogeneity of meroterpenoids arising from their dual biosynthetic origins is constantly provoking...
The divergent total synthesis strategy can be successfully applied to the preparation of families of...
Synthetic efforts towards various meroterpenoid natural products based on biosynthetic speculation w...
International audienceThis account reports a program of synthesis of aureothin from genesis to concl...
Here, we report a formal synthesis of the marine cytotoxic meroterpenoid actinoranone. Key steps inc...