Electrochemically generated tetraethylammonium peroxydicarbonate (TEAPC) and tetraethylammonium carbonate (TEAC) react under very mild conditions, with 1,2-amino alcohols affording, after addition of tosyl chloride, the corresponding oxazolidin-2-ones in fair to good yields. (C) 1999 Elsevier Science Ltd. All rights reserved
A new method for N-acryloylation of Evans' chiral auxiliaries (oxazolidin-2-ones) with alpha,alpha '...
An improved and efficient electrochemical N-acylation of chiral oxazolidin-2-ones has been achieved....
A synthetic method to prepare oxazol-2(3H)-ones and 5-alkenyloxazolidin-2-ones efficiently that reli...
An improved electrochemical synthesis of chiral oxazolidin-2-ones from chiral 1,2-amino alcohols is ...
The study of the reactivity of 1,2-amino alcohols toward carbon dioxide in the presence of 2-pyrro...
The study of the reactivity of 1,2-amino alcohols toward carbon dioxide in the presence of 2-pyrroli...
A simple electrochemical method for the synthesis and N-acylation of chiral oxazolidin-2-ones (Eva...
A new procedure for an efficient synthesis of oxazolidin-2-ones was developed. 2-Amino-1-alkanols un...
An efficient electrochemical synthesis of 5-methylene-1,3-oxazolidin-2-ones (2a-h) from acetylenic a...
An efficient electrochemical synthesis of 5-methylene-1,3-oxazolidin-2-ones (2a-h) from acetylenic a...
In this communication we describe a straightforward and diastereoselective approach to prepare funct...
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 ,-di...
A new synthesis of N-enoyloxazolidin-2-ones has been performed by electrochemical reduction of ,7-di...
A mild and efficient electrochemical alternative to classical base-catalyzed conjugate addition of n...
A new method for N-acryloylation of Evans' chiral auxiliaries (oxazolidin-2-ones) with alpha,alpha '...
An improved and efficient electrochemical N-acylation of chiral oxazolidin-2-ones has been achieved....
A synthetic method to prepare oxazol-2(3H)-ones and 5-alkenyloxazolidin-2-ones efficiently that reli...
An improved electrochemical synthesis of chiral oxazolidin-2-ones from chiral 1,2-amino alcohols is ...
The study of the reactivity of 1,2-amino alcohols toward carbon dioxide in the presence of 2-pyrro...
The study of the reactivity of 1,2-amino alcohols toward carbon dioxide in the presence of 2-pyrroli...
A simple electrochemical method for the synthesis and N-acylation of chiral oxazolidin-2-ones (Eva...
A new procedure for an efficient synthesis of oxazolidin-2-ones was developed. 2-Amino-1-alkanols un...
An efficient electrochemical synthesis of 5-methylene-1,3-oxazolidin-2-ones (2a-h) from acetylenic a...
An efficient electrochemical synthesis of 5-methylene-1,3-oxazolidin-2-ones (2a-h) from acetylenic a...
In this communication we describe a straightforward and diastereoselective approach to prepare funct...
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 ,-di...
A new synthesis of N-enoyloxazolidin-2-ones has been performed by electrochemical reduction of ,7-di...
A mild and efficient electrochemical alternative to classical base-catalyzed conjugate addition of n...
A new method for N-acryloylation of Evans' chiral auxiliaries (oxazolidin-2-ones) with alpha,alpha '...
An improved and efficient electrochemical N-acylation of chiral oxazolidin-2-ones has been achieved....
A synthetic method to prepare oxazol-2(3H)-ones and 5-alkenyloxazolidin-2-ones efficiently that reli...
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