Title of article
Access to enantiopure polycyclic β-lactams by Diels–Alder reaction of novel inner-outer-ring 2-(silyloxy)dienes with a carbacepham skeleton
Author/Authors
Alcaide، نويسنده , , Benito and de Murga، نويسنده , , Rosa M. and Pardo، نويسنده , , Carmen and Rodrيguez-Ranera، نويسنده , , Carolina، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2004
Pages
5
From page
7255
To page
7259
Abstract
The synthesis of unprecedented inner-outer-ring 2-[tert-butyldimethylsilyloxy]dienes with a carbacepham structure in optically pure form and their totally π-facial endo selective Diels–Alder reactions to structurally novel polycyclic β-lactams is reported.
Keywords
?-Lactam , 2-azetidinone , Carbacepham , Diene , Diels–Alder cycloaddition
Journal title
Tetrahedron Letters
Serial Year
2004
Journal title
Tetrahedron Letters
Record number
1843345
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