Title of article
Single pot diastereoselective synthesis of six membered cyclic (E)-endo-aldonitrones via intramolecular cyclization of ω-alkenyl oximes
Author/Authors
Mehra، نويسنده , , Vishu and Kumar، نويسنده , , Vipan، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2014
Pages
4
From page
845
To page
848
Abstract
β-Lactam-synthon interceded diastereoselective single pot synthesis of synthetically challenging six-membered cyclic (E)-endo-aldonitrones has been developed via intramolecular cyclization of ω-alkenyl oximes tethered at the C-3 position of 2-azetidinones along with its utilization in 1,3-dipolar cycloaddition reaction with DMAD.
Keywords
Cyclic nitrones , ?-Lactam synthon protocol , ?-Alkenyl oximes , Intramolecular cyclization , 1 , 3-dipolar cycloaddition
Journal title
Tetrahedron Letters
Serial Year
2014
Journal title
Tetrahedron Letters
Record number
1887934
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