Title of article :
3-Bromo-propenyl acetate in organic synthesis: an expeditious route to 3-alkyl-4-acetoxy-5-iodomethyl isoxazolidines
Author/Authors :
Lombardo، نويسنده , , Marco and Rispoli، نويسنده , , Gabriele and Licciulli، نويسنده , , Sebastiano and Trombini، نويسنده , , Claudio and Dhavale، نويسنده , , Dilip D.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2005
Pages :
4
From page :
3789
To page :
3792
Abstract :
N-Trimethylsilyloxy-N-benzyl-1-alkyl-2-acetoxy-3-buten-1-amines 13, obtained in good yields and moderate diastereoselectivities by TMSOTf promoted α-acetoxyallylation of nitrones using metallic zinc and 3-bromo-propenyl acetate 11, are exploited in a stereospecific 5-exo-trig iodocyclization reaction to afford 4,5-cis-3-alkyl-4-acetoxy-5-iodomethyl isoxazolidines 14, promising starting materials for the synthesis of pyrrolidine azasugars.
Keywords :
Trimethylsilyl triflate , ?-Hydroxyallylation , iodocyclization , 4-Acetoxy-5-iodomethyl isoxazolidines , Nitrones
Journal title :
Tetrahedron Letters
Serial Year :
2005
Journal title :
Tetrahedron Letters
Record number :
1845776
Link To Document :
بازگشت