Title of article
Reactivity of oxonaphtoporphyrins. Efficient β-functionalization of the porphyrin ring on reaction with nitrogen or carbon nucleophiles
Author/Authors
Sébastien Richeter، نويسنده , , Sébastien and Jeandon، نويسنده , , Christophe and Ruppert، نويسنده , , Romain and Callot، نويسنده , , Henry J، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2001
Pages
4
From page
2103
To page
2106
Abstract
Oxonaphtoporphyrins show a 1,4 reactivity involving the conjugated pyrrole double bond, the addition being followed by oxidation or elimination leading to rearomatization. Addition of nitrogen or carbon nucleophiles gives amino and substituted aminoporphyrins, or alkyl and cyanoporphyrins, respectively.
Journal title
Tetrahedron Letters
Serial Year
2001
Journal title
Tetrahedron Letters
Record number
1643750
Link To Document