This thesis describes the synthesis of novel thiacrown and azacrown ethers based on the 1.7-dioxaspiro[5.5] undecane ring system. Each chapter discusses the research in some detail. Chapter five describes the attempted kinetic resolution of the spiroacetal moiety, to provide enantiopure starting material for the synthesis of non-racemic spiroacetal crown ethers. Three different approaches were investigated. Chapter six summarises the results achieved and discusses possible strategies emanating from these results
Spiroaminals are an understudied class of heterocycle. Recently, the Barrett group reported a relati...
(N,N)-spiroaminal is an interesting chemical motif yet it is neglected in synthetic research compar...
Many bioactive natural products contain a spiroketal moiety in their complex structure. Recently, si...
A novel class of thiacrown and azacrown ethers incorporating the 1,7-dioxaspiro[5.5]undecane spiroac...
We have developed a short, efficient and enantioselective synthesis of 1,4,7,10-tetraoxa- and 1,7-di...
MicroreviewInternational audienceThe 1-oxa-7-azaspiro[5.5]undecane, 1-oxa-6-azaspiro[4.5]decane, 1-o...
Different chiral spiroketal skeletons are obtained, in a versatile manner, by iterative alkylations ...
(Chemical Equation Presented) A new approach to enantiomerically pure 2,8-dialkyl-1,7-dioxaspiro[5.5...
Publication details, including instructions for authors and subscription information
A novel chlorohydrin-based spirocyclization reaction has been developed that complements contemporar...
A new approach to enantiomerically pure 2,8-dialkyl-1,7-dioxaspiro[5.5]undecanes and 2,7-dialkyl-1,6...
A convergent and stereoselective synthesis of 1-oxa-7-azaspiro[5.5]undecane is described. This funct...
The synthesis and cyclisation of 3-methyl-4-methylene-3-(3-diazo-3-methoxycarbonyl-2-oxopropyl)-1-cy...
The spiroketal moiety forms a part of the skeleton of many natural products that present various bio...
Alkylidenation of lactones with functionalised titanium carbenoid reagents (Schrock carbenes) follow...
Spiroaminals are an understudied class of heterocycle. Recently, the Barrett group reported a relati...
(N,N)-spiroaminal is an interesting chemical motif yet it is neglected in synthetic research compar...
Many bioactive natural products contain a spiroketal moiety in their complex structure. Recently, si...
A novel class of thiacrown and azacrown ethers incorporating the 1,7-dioxaspiro[5.5]undecane spiroac...
We have developed a short, efficient and enantioselective synthesis of 1,4,7,10-tetraoxa- and 1,7-di...
MicroreviewInternational audienceThe 1-oxa-7-azaspiro[5.5]undecane, 1-oxa-6-azaspiro[4.5]decane, 1-o...
Different chiral spiroketal skeletons are obtained, in a versatile manner, by iterative alkylations ...
(Chemical Equation Presented) A new approach to enantiomerically pure 2,8-dialkyl-1,7-dioxaspiro[5.5...
Publication details, including instructions for authors and subscription information
A novel chlorohydrin-based spirocyclization reaction has been developed that complements contemporar...
A new approach to enantiomerically pure 2,8-dialkyl-1,7-dioxaspiro[5.5]undecanes and 2,7-dialkyl-1,6...
A convergent and stereoselective synthesis of 1-oxa-7-azaspiro[5.5]undecane is described. This funct...
The synthesis and cyclisation of 3-methyl-4-methylene-3-(3-diazo-3-methoxycarbonyl-2-oxopropyl)-1-cy...
The spiroketal moiety forms a part of the skeleton of many natural products that present various bio...
Alkylidenation of lactones with functionalised titanium carbenoid reagents (Schrock carbenes) follow...
Spiroaminals are an understudied class of heterocycle. Recently, the Barrett group reported a relati...
(N,N)-spiroaminal is an interesting chemical motif yet it is neglected in synthetic research compar...
Many bioactive natural products contain a spiroketal moiety in their complex structure. Recently, si...