Title of article :
X=Y–ZH Systems as potential 1,3-dipoles. Part 52: Fused-ring forming electrophile induced oxime→nitrone→cycloaddition cascades
Author/Authors :
H Ali Dondas، نويسنده , , Ronald Grigg، نويسنده , , Sylvie Thibault، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2001
Pages :
11
From page :
7035
To page :
7045
Abstract :
Electrophile induced cyclisation of oximes onto endocyclic alkenes and exo-methylene cycloalkanes occurs stereo- and regio-specifically generating cis-fused bicyclic nitrones in good yield. Subsequent facially selective cycloaddition with N-methylmaleimide occurs in good yield. The sequence may be carried out as a one-pot procedure and results in the formation of 4 bonds, 2 rings and 6 stereocentres.
Keywords :
1 , cyclic nitrones , cycloalkenes , facial selectivity , 3-dipolar cycloaddition , exo- and endo-trig cyclisation , onium ions
Journal title :
Tetrahedron
Serial Year :
2001
Journal title :
Tetrahedron
Record number :
1082312
Link To Document :
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