Title of article :
2,3-Dihydro-1H-1,3-diazepin-2-ones: synthesis and novel rearrangements into pyrrole derivatives
Author/Authors :
Fesenko، نويسنده , , Anastasia A. and Shutalev، نويسنده , , Anatoly D.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2014
Pages :
5
From page :
1416
To page :
1420
Abstract :
A novel synthesis of 2,3-dihydro-1H-1,3-diazepin-2-ones based on thermal elimination of methanol from 4-methoxy-2,3,4,5-tetrahydro-1H-1,3-diazepin-2-ones has been developed. The prepared dihydrodiazepinones underwent two new rearrangements under basic or acidic conditions to give the pyrrole derivatives, 3-(aminomethylene)-2,3-dihydro-1H-pyrrol-2-ones and 1-carbamoyl-1H-pyrroles, respectively. Plausible mechanisms for the rearrangements are proposed.
Keywords :
Ring contraction , Anti-aromaticity , 3-Dihydro-1H-pyrrol-2-ones , 3-diazepin-2-ones , 1H-Pyrroles , 1H-1 , 2
Journal title :
Tetrahedron Letters
Serial Year :
2014
Journal title :
Tetrahedron Letters
Record number :
1888245
Link To Document :
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