Title of article
An expedient route to diaza-spirocycles utilizing a sequential multicomponent α-aminoallylation/ring-closing metathesis strategy
Author/Authors
Gracias، نويسنده , , Vijaya and Gasiecki، نويسنده , , Alan F. and Moore، نويسنده , , Joel D. and Akritopoulou-Zanze، نويسنده , , Irini and Djuric، نويسنده , , Stevan W.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2006
Pages
4
From page
8977
To page
8980
Abstract
A general method for the preparation of diaza-spirocycles is reported. This method used an olefin metathesis in order to construct the desired spirocyclic framework. Beginning with commercially available protected amino ketones, this strategy ultimately produced pharmacologically relevant diaza-scaffolds in an efficient and high-yielding process.
Journal title
Tetrahedron Letters
Serial Year
2006
Journal title
Tetrahedron Letters
Record number
1853607
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