Total synthesis of the Rhododendron meroterpenoids rubiginosins A and G, which both contain unusual 6-6-6-4 ring systems, has been achieved using a bioinspired cascade approach. Stepwise synthesis of these natural products, and the related 6-6-5-4 meroterpenoids fastinoid B and rhodonoid B, from naturally occurring chromene precursors is also reported.Laura Burchill, Aaron J. Day, Oussama Yahiaoui, and Jonathan H. Georg
A scalable, divergent synthesis of bioactive meroterpenoids has been developed. A key component of t...
A scalable, divergent synthesis of bioactive meroterpenoids has been developed. A key component of t...
The first total synthesis of five austalide natural products, (±)-17S-dihydroaustalide K, (±)-austal...
A divergent, three-step total synthesis of rhodonoids C and D has been achieved using a biosynthetic...
The discipline of natural product synthesis serves to provide a platform for reaction discovery, the...
Conspectus Natural products are biosynthesized from a limited pool of starting materials via pathway...
Synthetic efforts towards various meroterpenoid natural products based on biosynthetic speculation w...
Heterogeneity of meroterpenoids arising from their dual biosynthetic origins is constantly provoking...
Heterogeneity of meroterpenoids arising from their dual biosynthetic origins is constantly provoking...
This thesis outlines synthetic efforts towards three different natural product families. Norascyrono...
Structural reassignments for littordial E, littordial F, and drychampone B are proposed on the basis...
A series of cascade reactions of o-quinone methides have been developed based on the proposed biosyn...
The primary aim of this project was to develop total syntheses of natural products kamalachalcone A ...
This thesis describes several syntheses of natural products. The overall synthetic approach is to mi...
A scalable, divergent synthesis of bioactive meroterpenoids has been developed. A key component of t...
A scalable, divergent synthesis of bioactive meroterpenoids has been developed. A key component of t...
A scalable, divergent synthesis of bioactive meroterpenoids has been developed. A key component of t...
The first total synthesis of five austalide natural products, (±)-17S-dihydroaustalide K, (±)-austal...
A divergent, three-step total synthesis of rhodonoids C and D has been achieved using a biosynthetic...
The discipline of natural product synthesis serves to provide a platform for reaction discovery, the...
Conspectus Natural products are biosynthesized from a limited pool of starting materials via pathway...
Synthetic efforts towards various meroterpenoid natural products based on biosynthetic speculation w...
Heterogeneity of meroterpenoids arising from their dual biosynthetic origins is constantly provoking...
Heterogeneity of meroterpenoids arising from their dual biosynthetic origins is constantly provoking...
This thesis outlines synthetic efforts towards three different natural product families. Norascyrono...
Structural reassignments for littordial E, littordial F, and drychampone B are proposed on the basis...
A series of cascade reactions of o-quinone methides have been developed based on the proposed biosyn...
The primary aim of this project was to develop total syntheses of natural products kamalachalcone A ...
This thesis describes several syntheses of natural products. The overall synthetic approach is to mi...
A scalable, divergent synthesis of bioactive meroterpenoids has been developed. A key component of t...
A scalable, divergent synthesis of bioactive meroterpenoids has been developed. A key component of t...
A scalable, divergent synthesis of bioactive meroterpenoids has been developed. A key component of t...
The first total synthesis of five austalide natural products, (±)-17S-dihydroaustalide K, (±)-austal...