A synthesis of cyanolide A, a diolide natural product, has been achieved using a diastereoselective Barbier reaction, early-stage glycosylation, and intramolecular oxa-Michael addition to form the THP ring.Accepted versio
A strategy to control the diastereoselectivity of bond formation at a prochiral attached-ring bridge...
A strategy to control the diastereoselectivity of bond formation at a prochiral attached-ring bridge...
The goal of this thesis was the asymmetric synthesis of natural products. These were Synargentoide A...
The introduction of the chapter highlights the application of natural product synthesis via syntheti...
Formal total synthesis of cyanolide A, aglycosidic dimeric macrolide is accomplished. The key reacti...
This thesis describes the implementation of the intramolecular Barbier reaction in the diastereosele...
The intramolecular hetero-Michael addition is one of the most convergent strategies for the synthesi...
The intramolecular hetero-Michael addition is one of the most convergent strategies for the synthesi...
This thesis describes the implementation of the intramolecular Barbier reaction in the diastereosele...
A modular synthesis of the reportedly potent molluscicide, cyanolide A, was developed to provide fac...
An organic synthesis ‘round trip’ between natural product total synthesis and the development of new...
An organic synthesis ‘round trip’ between natural product total synthesis and the development of new...
The diastereoselective intramolecular Michael addition of the benzylamine generated in situ from hem...
Polyhydroxylated fragments are ubiquitous in natural products possessing interesting biological prop...
The first chapter describes the synthesis of curvulone B featuring a strategy of cross metathesis an...
A strategy to control the diastereoselectivity of bond formation at a prochiral attached-ring bridge...
A strategy to control the diastereoselectivity of bond formation at a prochiral attached-ring bridge...
The goal of this thesis was the asymmetric synthesis of natural products. These were Synargentoide A...
The introduction of the chapter highlights the application of natural product synthesis via syntheti...
Formal total synthesis of cyanolide A, aglycosidic dimeric macrolide is accomplished. The key reacti...
This thesis describes the implementation of the intramolecular Barbier reaction in the diastereosele...
The intramolecular hetero-Michael addition is one of the most convergent strategies for the synthesi...
The intramolecular hetero-Michael addition is one of the most convergent strategies for the synthesi...
This thesis describes the implementation of the intramolecular Barbier reaction in the diastereosele...
A modular synthesis of the reportedly potent molluscicide, cyanolide A, was developed to provide fac...
An organic synthesis ‘round trip’ between natural product total synthesis and the development of new...
An organic synthesis ‘round trip’ between natural product total synthesis and the development of new...
The diastereoselective intramolecular Michael addition of the benzylamine generated in situ from hem...
Polyhydroxylated fragments are ubiquitous in natural products possessing interesting biological prop...
The first chapter describes the synthesis of curvulone B featuring a strategy of cross metathesis an...
A strategy to control the diastereoselectivity of bond formation at a prochiral attached-ring bridge...
A strategy to control the diastereoselectivity of bond formation at a prochiral attached-ring bridge...
The goal of this thesis was the asymmetric synthesis of natural products. These were Synargentoide A...
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