A RhIII‐catalyzed intramolecular oxidative cross‐coupling between double bonds for the synthesis of macrolides is described. Under the optimized reaction conditions, macrocycles containing a diene moiety can be formed in reasonable yields and with excellent chemo‐ and stereoselectivity. This method provides an efficient approach to synthesize macrocyclic compounds containing a 1,3‐conjugated diene structure
The design and synthesis of head-to-tail linked artificial macrocycles using the Ugi-reaction has be...
Macrocycles are key structural elements in numerous bioactive small molecules and are attractive tar...
The design and synthesis of head-to-tail linked artificial macrocycles using the Ugi-reaction has be...
A tandem dimerization/macrocyclization reaction utilizing the Prins cyclization has been developed. ...
Macrocyclic scaffolds are commonly found in bioactive natural products and pharmaceutical molecules....
A short reaction pathway was devised to synthesize a library of artificial 18-27-membered macrocycle...
Manganese(III)-based oxidative free-radical macrocyclization was examined. α,α,ω,ω-Tetraaryl-α,ω-alk...
Manganese(III)-based oxidative free-radical macrocyclization was examined. α,α,ω,ω-Tetraaryl-α,ω-alk...
A copper-mediated macrocyclization involving the reaction of a vinyl iodide and a terminal alkyne fo...
Macrocycles are commonly synthesized via late-stage macrolactamization and macrolactonization. Strat...
A new synthetic strategy for macrocycles bearing multiple coordination moieties was developed. A sel...
Artificial macrocycles can be convergently synthesized by a sequence of an Ugi multicomponent reacti...
Transition metal-mediated synthesis and functionalization of macrocycles were investigated. A novel ...
Manganese(III)-based macrocyclization of alkadienes with bis(3-oxobutanoate)s was investigated and m...
Manganese(III)-based macrocyclization of alkadienes with bis(3-oxobutanoate)s was investigated and m...
The design and synthesis of head-to-tail linked artificial macrocycles using the Ugi-reaction has be...
Macrocycles are key structural elements in numerous bioactive small molecules and are attractive tar...
The design and synthesis of head-to-tail linked artificial macrocycles using the Ugi-reaction has be...
A tandem dimerization/macrocyclization reaction utilizing the Prins cyclization has been developed. ...
Macrocyclic scaffolds are commonly found in bioactive natural products and pharmaceutical molecules....
A short reaction pathway was devised to synthesize a library of artificial 18-27-membered macrocycle...
Manganese(III)-based oxidative free-radical macrocyclization was examined. α,α,ω,ω-Tetraaryl-α,ω-alk...
Manganese(III)-based oxidative free-radical macrocyclization was examined. α,α,ω,ω-Tetraaryl-α,ω-alk...
A copper-mediated macrocyclization involving the reaction of a vinyl iodide and a terminal alkyne fo...
Macrocycles are commonly synthesized via late-stage macrolactamization and macrolactonization. Strat...
A new synthetic strategy for macrocycles bearing multiple coordination moieties was developed. A sel...
Artificial macrocycles can be convergently synthesized by a sequence of an Ugi multicomponent reacti...
Transition metal-mediated synthesis and functionalization of macrocycles were investigated. A novel ...
Manganese(III)-based macrocyclization of alkadienes with bis(3-oxobutanoate)s was investigated and m...
Manganese(III)-based macrocyclization of alkadienes with bis(3-oxobutanoate)s was investigated and m...
The design and synthesis of head-to-tail linked artificial macrocycles using the Ugi-reaction has be...
Macrocycles are key structural elements in numerous bioactive small molecules and are attractive tar...
The design and synthesis of head-to-tail linked artificial macrocycles using the Ugi-reaction has be...