An efficient, oxidative cleavage of a sulfur linker has been developed for the fluorousphase synthesis of N-heterocycles. The new cleavage strategy facilitates the synthesis ofproducts containing diverse structural features
Fluorine-containing organic scaffolds are of significant interest in medicinal chemistry. The incorp...
Solid phase organic synthesis is a powerful technique to facilitate rapid synthesis and easy purific...
Fluorous molecules partition out of an organic phase and into a fluorous (highly fluorinated) phase ...
A fluorous, cyclative-capture strategy, based on a connective Pummerer-type process, has been develo...
Linker strategies lie at the heart of solid phase organic synthesis and combinatorial chemistry. A n...
A fluorous-tagged “safety catch” linker is described for the synthesis of heterocycles with use of r...
A new approach to fused N,S-heterocycles is described. Treatment of N-(2-(alkylsulfinyl)phenyl)pyrro...
A fluorous-linker-assisted solution-phase protocol has been developed and applied to parallel synthe...
Virtually inert sulfur hexafluoride becomes a precious pentafluorosulfanylation agent, if properly a...
Fluorous reagents and reactants provide emerging new options in parallel synthesis because they are ...
The phase-vanishing (PV) method is based on spontaneous reaction controlled by diffusion of reagents...
A series of novel 7-membered cyclic sulfonamides and sulfamides were prepared in good to excellent y...
The phase-vanishing (PV) method is based on spontaneous reaction controlled by diffusion of reagents...
A fluorous-linker-assisted solution-phase protocol has been developed and applied to parallel synthe...
This work concerns the investigation of new synthetic routes to heterocycles via a building block st...
Fluorine-containing organic scaffolds are of significant interest in medicinal chemistry. The incorp...
Solid phase organic synthesis is a powerful technique to facilitate rapid synthesis and easy purific...
Fluorous molecules partition out of an organic phase and into a fluorous (highly fluorinated) phase ...
A fluorous, cyclative-capture strategy, based on a connective Pummerer-type process, has been develo...
Linker strategies lie at the heart of solid phase organic synthesis and combinatorial chemistry. A n...
A fluorous-tagged “safety catch” linker is described for the synthesis of heterocycles with use of r...
A new approach to fused N,S-heterocycles is described. Treatment of N-(2-(alkylsulfinyl)phenyl)pyrro...
A fluorous-linker-assisted solution-phase protocol has been developed and applied to parallel synthe...
Virtually inert sulfur hexafluoride becomes a precious pentafluorosulfanylation agent, if properly a...
Fluorous reagents and reactants provide emerging new options in parallel synthesis because they are ...
The phase-vanishing (PV) method is based on spontaneous reaction controlled by diffusion of reagents...
A series of novel 7-membered cyclic sulfonamides and sulfamides were prepared in good to excellent y...
The phase-vanishing (PV) method is based on spontaneous reaction controlled by diffusion of reagents...
A fluorous-linker-assisted solution-phase protocol has been developed and applied to parallel synthe...
This work concerns the investigation of new synthetic routes to heterocycles via a building block st...
Fluorine-containing organic scaffolds are of significant interest in medicinal chemistry. The incorp...
Solid phase organic synthesis is a powerful technique to facilitate rapid synthesis and easy purific...
Fluorous molecules partition out of an organic phase and into a fluorous (highly fluorinated) phase ...