The enantioselective synthesis of bistramide A has been achieved with a longest linear sequence of 18 steps. The synthetic strategy involves the use of a distereoselective glycolate alkylation, an aldol addition of a chlorotitanium enolate of N-acylthiazolidinthione, and a Sharpless asymmetric epoxidation to synthesize the three key fragments
The thesis entitled “Enantioselective synthesis of bio-active bicyclic acetals, cyclic ethers and la...
The research presented herein explores three aspects of asymmetric catalysis: (1) the development of...
A concise formal synthesis of the cytotoxic macrolides (-)-salicylihalamides A and B is reported. Ke...
The enantioselective synthesis of bistramide A has been achieved with a longest linear sequence of 1...
The bistramides are a class of natural products isolated from the marine ascidian Lissoclinum bistra...
L'étude des molécules issues du milieu naturel a conduit les chercheurs à s'intéresser à la synthèse...
After the isolation of the bioactive polyether bistramide C from the marine ascidian Lissoclinum bis...
The enantioselective synthesis of FD-891 has been achieved with a longest linear sequence of 21 step...
International audienceThe total synthesis of spiromastilactone A is reported for the first time. A s...
The first chapter describes our preparation of novel analogs of the natural product, palmarumycin CP...
The enantioselective total synthesis of spirofungins A (1) and B (2) is reported in 14 steps over th...
Bistramide D is a member of new class of bioactive molecule isolated from the marine ascidian Lissoc...
In this thesis we will disclose the results obtained from the diastereoisomeric salt formation (n sa...
Synthesis of the C1-C6 and C7-C23 fragments of the proposed structure of iriomoteolide 1a has been a...
The authors thank the Royal Society for a University Research Fellowship (ADS), the EPSRC (EP/J01813...
The thesis entitled “Enantioselective synthesis of bio-active bicyclic acetals, cyclic ethers and la...
The research presented herein explores three aspects of asymmetric catalysis: (1) the development of...
A concise formal synthesis of the cytotoxic macrolides (-)-salicylihalamides A and B is reported. Ke...
The enantioselective synthesis of bistramide A has been achieved with a longest linear sequence of 1...
The bistramides are a class of natural products isolated from the marine ascidian Lissoclinum bistra...
L'étude des molécules issues du milieu naturel a conduit les chercheurs à s'intéresser à la synthèse...
After the isolation of the bioactive polyether bistramide C from the marine ascidian Lissoclinum bis...
The enantioselective synthesis of FD-891 has been achieved with a longest linear sequence of 21 step...
International audienceThe total synthesis of spiromastilactone A is reported for the first time. A s...
The first chapter describes our preparation of novel analogs of the natural product, palmarumycin CP...
The enantioselective total synthesis of spirofungins A (1) and B (2) is reported in 14 steps over th...
Bistramide D is a member of new class of bioactive molecule isolated from the marine ascidian Lissoc...
In this thesis we will disclose the results obtained from the diastereoisomeric salt formation (n sa...
Synthesis of the C1-C6 and C7-C23 fragments of the proposed structure of iriomoteolide 1a has been a...
The authors thank the Royal Society for a University Research Fellowship (ADS), the EPSRC (EP/J01813...
The thesis entitled “Enantioselective synthesis of bio-active bicyclic acetals, cyclic ethers and la...
The research presented herein explores three aspects of asymmetric catalysis: (1) the development of...
A concise formal synthesis of the cytotoxic macrolides (-)-salicylihalamides A and B is reported. Ke...