Title of article
An efficient 1,2,4-triazine-based route to the louisianin alkaloids
Author/Authors
Linda Catozzi، نويسنده , , Nicola and Wasnaire، نويسنده , , Pierre and Taylor، نويسنده , , Richard J.K.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2008
Pages
4
From page
2865
To page
2868
Abstract
A new, short and efficient route to louisianins C and D is described in which the pyridine ring is constructed from a disubstituted 1,2,4-triazine by an inverse-electron-demand Diels–Alder/retro-Diels–Alder/aromatisation cascade sequence. This eight-step route produces louisianin C in 16% overall yield from the commercially available 5-chloropent-1-yne.
Journal title
Tetrahedron Letters
Serial Year
2008
Journal title
Tetrahedron Letters
Record number
1859053
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