2-Methyleneaziridines can be transformed into 5,5'-disubstituted hydantoins in moderate to good yield (48-75%) via a lone-pot' process that brings together up to six components in an orchestrated way. (c) 2006 Elsevier Ltd. All rights reserved
This account describes the development of methyleneaziridines as heterocyclic building blocks for a ...
Access to combinatorial chemistry of hydantoins is provided by convenient and versatile methods for ...
Multicomponent reactions (MCRs) are a powerful tool for the synthesis of complex molecules starting ...
The development of new practical and green methods for the synthesis of small heterocycles is an att...
Triazinane diones, readily generated by a recently reported multicomponent reaction, can be easily a...
A novel, three-component process for the preparation of a small library of unprecedented nonracemic ...
Multicomponent reactions (MCRs) are versatile syntheses for obtaining structurally diverse sets of c...
A general and efficient method for the synthesis of drug-like fused bicyclic hydantoins is reported....
Methyleneaziridines can be converted into a wide range of 1,2-diamines and 2-cyanopiperidines in a s...
The Bucherer-Bergs reaction is a classical multi-component reaction that yields hydantoins, which ca...
An efficient and straightforward two-step procedure for the synthesis of N-1 alkyl/aryl-substituted ...
Multicomponent reactions are a powerful tool in the synthesis of complex target molecules because mu...
Diverse sets of 5,5'-disubstituted hydantoins can conveniently be made in moderate to good yields (4...
Hydantoins are an important class of heterocycles with applications in pharmacy, agriculture, and as...
Hydantoins are an important class of heterocycles with applications in pharmacy, agriculture, and as...
This account describes the development of methyleneaziridines as heterocyclic building blocks for a ...
Access to combinatorial chemistry of hydantoins is provided by convenient and versatile methods for ...
Multicomponent reactions (MCRs) are a powerful tool for the synthesis of complex molecules starting ...
The development of new practical and green methods for the synthesis of small heterocycles is an att...
Triazinane diones, readily generated by a recently reported multicomponent reaction, can be easily a...
A novel, three-component process for the preparation of a small library of unprecedented nonracemic ...
Multicomponent reactions (MCRs) are versatile syntheses for obtaining structurally diverse sets of c...
A general and efficient method for the synthesis of drug-like fused bicyclic hydantoins is reported....
Methyleneaziridines can be converted into a wide range of 1,2-diamines and 2-cyanopiperidines in a s...
The Bucherer-Bergs reaction is a classical multi-component reaction that yields hydantoins, which ca...
An efficient and straightforward two-step procedure for the synthesis of N-1 alkyl/aryl-substituted ...
Multicomponent reactions are a powerful tool in the synthesis of complex target molecules because mu...
Diverse sets of 5,5'-disubstituted hydantoins can conveniently be made in moderate to good yields (4...
Hydantoins are an important class of heterocycles with applications in pharmacy, agriculture, and as...
Hydantoins are an important class of heterocycles with applications in pharmacy, agriculture, and as...
This account describes the development of methyleneaziridines as heterocyclic building blocks for a ...
Access to combinatorial chemistry of hydantoins is provided by convenient and versatile methods for ...
Multicomponent reactions (MCRs) are a powerful tool for the synthesis of complex molecules starting ...
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