An improved and efficient electrochemical N- acylation of chiral oxazolidin-2-ones has been achieved. The generation of the nitrogen anion is obtained under mild conditions and without addition of base or probase, by direct electrolysis of a solution of MeCN-TEAP containing the oxazolidinone. Acylation agents (acid chlorides or anhy- drides) were added at the end of the electrolysis. N-Acylated products were isolated in high to excellent yields
A new electrochemical method for the mild generation of naked -dicarbonyl derivative enolates is dis...
In an attempt to form 2-alkylidene-1,3-oxazolidines, chiral 2-oxazolines have been N-alkylated and N...
A series of three 5,5-diaryl substituted oxazolidin-2-ones (diphenyl, dinaphthyl and ditolyl) have b...
An improved and efficient electrochemical N-acylation of chiral oxazolidin-2-ones has been achieved....
The study of the reactivity of oxazolidin-2-ones versus acylating agents (anhydrides or acyl chlorid...
A simple electrochemical method for the synthesis and N-acylation of chiral oxazolidin-2-ones (Eva...
A new method for N-acryloylation of Evans’ chiral auxiliaries (oxazolidin-2-ones) with α,α-dichlor...
A mild and efficient electrochemical alternative to classical base-catalyzed conjugate addition of n...
An electrochemical procedure for the N-acylation of chiral oxazolidin-2-ones, in the absence of vola...
An improved electrochemical synthesis of chiral oxazolidin-2-ones from chiral 1,2-amino alcohols is ...
A new synthesis of N -enoyloxazolidin-2-ones has been performed by electrochemical reduction of ,-di...
A new synthesis of N-enoyloxazolidin-2-ones has been performed by electrochemical reduction of alpha...
A new synthesis of N-enoyloxazolidin-2-ones has been performed by electrochemical reduction of ,7-di...
The electrochemical generation of chiral enolates is here described, either by cathodic reduction ...
A new electrochemical method for the mild generation of naked \u98-dicarbonyl derivative enolates is...
A new electrochemical method for the mild generation of naked -dicarbonyl derivative enolates is dis...
In an attempt to form 2-alkylidene-1,3-oxazolidines, chiral 2-oxazolines have been N-alkylated and N...
A series of three 5,5-diaryl substituted oxazolidin-2-ones (diphenyl, dinaphthyl and ditolyl) have b...
An improved and efficient electrochemical N-acylation of chiral oxazolidin-2-ones has been achieved....
The study of the reactivity of oxazolidin-2-ones versus acylating agents (anhydrides or acyl chlorid...
A simple electrochemical method for the synthesis and N-acylation of chiral oxazolidin-2-ones (Eva...
A new method for N-acryloylation of Evans’ chiral auxiliaries (oxazolidin-2-ones) with α,α-dichlor...
A mild and efficient electrochemical alternative to classical base-catalyzed conjugate addition of n...
An electrochemical procedure for the N-acylation of chiral oxazolidin-2-ones, in the absence of vola...
An improved electrochemical synthesis of chiral oxazolidin-2-ones from chiral 1,2-amino alcohols is ...
A new synthesis of N -enoyloxazolidin-2-ones has been performed by electrochemical reduction of ,-di...
A new synthesis of N-enoyloxazolidin-2-ones has been performed by electrochemical reduction of alpha...
A new synthesis of N-enoyloxazolidin-2-ones has been performed by electrochemical reduction of ,7-di...
The electrochemical generation of chiral enolates is here described, either by cathodic reduction ...
A new electrochemical method for the mild generation of naked \u98-dicarbonyl derivative enolates is...
A new electrochemical method for the mild generation of naked -dicarbonyl derivative enolates is dis...
In an attempt to form 2-alkylidene-1,3-oxazolidines, chiral 2-oxazolines have been N-alkylated and N...
A series of three 5,5-diaryl substituted oxazolidin-2-ones (diphenyl, dinaphthyl and ditolyl) have b...