Synthetic approaches towards 4,10-diaza-1,7-dioxaspiro[5.5]undecanes starting from 1,3-dichloroacetone and solketal derivatives are explored. The method relies on the preparation of a key bis-substituted dihydroxy-protected oxime, which would undergo a final acidic deprotection–spiroacetalization process. Although the desired diazaspiroketal framework could not be obtained, our conditions led to the unexpected 3-aza-6,8-dioxabicyclo[3.2.1]octan-2-one 18 or to the oxazinone 32 in good yields
4,5-Diazaspiro[2.3]hexanes are made by dihalocarbene addition across the exocyclic double bond of re...
Many bioactive natural products contain a spiroketal moiety in their complex structure. Recently, si...
© 2015 Elsevier Ltd. All rights reserved. Functionalised azepane and oxepane scaffolds were prepared...
Synthetic approaches towards 4,10-diaza-1,7-dioxaspiro[5.5]undecanes starting from 1,3-dichloroaceto...
International audienceThis work describes a modular efficient route to 10-aza-4-thia-, 10-aza-4-oxa-...
The spiroketal moiety forms a part of the skeleton of many natural products that present various bio...
MicroreviewInternational audienceThe 1-oxa-7-azaspiro[5.5]undecane, 1-oxa-6-azaspiro[4.5]decane, 1-o...
(N,N)-spiroaminal is an interesting chemical motif yet it is neglected in synthetic research compar...
We have developed a short, efficient and enantioselective synthesis of 1,4,7,10-tetraoxa- and 1,7-di...
Spiroaminals are an understudied class of heterocycle. Recently, the Barrett group reported a relati...
A simple two-step sequence is used to efficiently make novel spirocyclic analogues of the diketopipe...
The nitrogen containing spiro-heterocycle is one of the privileged synthetic motif that constitutes ...
AbstractThe nitrogen containing spiro-heterocycle is one of the privileged synthetic motif that cons...
A new route to spiro-oxetanes, potential scaffolds for drug discovery, is described. The route is ba...
A new route to spiro-oxetanes, potential scaffolds for drug discovery, is described. The route is ba...
4,5-Diazaspiro[2.3]hexanes are made by dihalocarbene addition across the exocyclic double bond of re...
Many bioactive natural products contain a spiroketal moiety in their complex structure. Recently, si...
© 2015 Elsevier Ltd. All rights reserved. Functionalised azepane and oxepane scaffolds were prepared...
Synthetic approaches towards 4,10-diaza-1,7-dioxaspiro[5.5]undecanes starting from 1,3-dichloroaceto...
International audienceThis work describes a modular efficient route to 10-aza-4-thia-, 10-aza-4-oxa-...
The spiroketal moiety forms a part of the skeleton of many natural products that present various bio...
MicroreviewInternational audienceThe 1-oxa-7-azaspiro[5.5]undecane, 1-oxa-6-azaspiro[4.5]decane, 1-o...
(N,N)-spiroaminal is an interesting chemical motif yet it is neglected in synthetic research compar...
We have developed a short, efficient and enantioselective synthesis of 1,4,7,10-tetraoxa- and 1,7-di...
Spiroaminals are an understudied class of heterocycle. Recently, the Barrett group reported a relati...
A simple two-step sequence is used to efficiently make novel spirocyclic analogues of the diketopipe...
The nitrogen containing spiro-heterocycle is one of the privileged synthetic motif that constitutes ...
AbstractThe nitrogen containing spiro-heterocycle is one of the privileged synthetic motif that cons...
A new route to spiro-oxetanes, potential scaffolds for drug discovery, is described. The route is ba...
A new route to spiro-oxetanes, potential scaffolds for drug discovery, is described. The route is ba...
4,5-Diazaspiro[2.3]hexanes are made by dihalocarbene addition across the exocyclic double bond of re...
Many bioactive natural products contain a spiroketal moiety in their complex structure. Recently, si...
© 2015 Elsevier Ltd. All rights reserved. Functionalised azepane and oxepane scaffolds were prepared...