For the rapid elaboration of polycarbocyclic scaffolds, prevalent in many important families of terpenoid natural products, allyl cations derived from simple heterocyclic alcohols can be used as versatile reaction partners in both (4+3) and (3+2) cycloaddition pathways. Our recent progress in this area is outlined, pointing towards the untapped potential of heterocycles to act as reagents in novel or known but challenging organic transformations
A novel Lewis acid-promoted (4+3) cycloaddition between a furfuryl alcohol and a diene was recently ...
Organic chemists have began to use intramolecular radical addition reactions i.e. radical cyclizatio...
A novel Lewis acid-promoted (4+3) cycloaddition between a furfuryl alcohol and a diene was recently ...
For the rapid elaboration of polycarbocyclic scaffolds, prevalent in many important families of terp...
For the rapid elaboration of polycarbocyclic scaffolds, prevalent in many important families of terp...
The title heterocyclic alcohol readily generates a sulfur-substituted allylic cation upon simple tre...
The title heterocyclic alcohol readily generates a sulfur-substituted allylic cation upon simple tre...
Allylic alcohol transposition lacks a thermodynamic driving force and usually displays stereo-infide...
Allylic alcohol transposition lacks a thermodynamic driving force and usually displays stereo-infide...
Cycloaddition reactions are powerful transformations for the construction of various cyclic organic ...
A Ti(Oi-Pr)4 promoted 5 or 6-endo-trig cyclisation to make nitrogen heterocycles is presented. The u...
Heterocycles are among the most common scaffolds in many organic molecules, e.g., vitamins, hormones...
A novel Lewis acid-promoted (4+3) cycloaddition between a furfuryl alcohol and a diene was recently ...
CONSPECTUS: The combination of two or more unsatu-rated structural units to form cyclic organic comp...
Enantiomerically highly enriched unsaturated β-ketoesters bearing a quaternary stereocenter can be u...
A novel Lewis acid-promoted (4+3) cycloaddition between a furfuryl alcohol and a diene was recently ...
Organic chemists have began to use intramolecular radical addition reactions i.e. radical cyclizatio...
A novel Lewis acid-promoted (4+3) cycloaddition between a furfuryl alcohol and a diene was recently ...
For the rapid elaboration of polycarbocyclic scaffolds, prevalent in many important families of terp...
For the rapid elaboration of polycarbocyclic scaffolds, prevalent in many important families of terp...
The title heterocyclic alcohol readily generates a sulfur-substituted allylic cation upon simple tre...
The title heterocyclic alcohol readily generates a sulfur-substituted allylic cation upon simple tre...
Allylic alcohol transposition lacks a thermodynamic driving force and usually displays stereo-infide...
Allylic alcohol transposition lacks a thermodynamic driving force and usually displays stereo-infide...
Cycloaddition reactions are powerful transformations for the construction of various cyclic organic ...
A Ti(Oi-Pr)4 promoted 5 or 6-endo-trig cyclisation to make nitrogen heterocycles is presented. The u...
Heterocycles are among the most common scaffolds in many organic molecules, e.g., vitamins, hormones...
A novel Lewis acid-promoted (4+3) cycloaddition between a furfuryl alcohol and a diene was recently ...
CONSPECTUS: The combination of two or more unsatu-rated structural units to form cyclic organic comp...
Enantiomerically highly enriched unsaturated β-ketoesters bearing a quaternary stereocenter can be u...
A novel Lewis acid-promoted (4+3) cycloaddition between a furfuryl alcohol and a diene was recently ...
Organic chemists have began to use intramolecular radical addition reactions i.e. radical cyclizatio...
A novel Lewis acid-promoted (4+3) cycloaddition between a furfuryl alcohol and a diene was recently ...