Article ID Journal Published Year Pages File Type
5289620 Tetrahedron Letters 2006 4 Pages PDF
Abstract
A conceptually simple H2-hydrogenation protocol is introduced for the high-yield preparation of a natural product derivative. Protoporphyrin IX dimethyl ester is hydrogenated to the mesoporphyrin analogue in N,N-dimethylacetamide under H2 (1 atm) at 80 °C within 30 min. The reaction is catalyzed by commercial RuCl3, without the need for the use of phosphine- and/or carbene-based ligands.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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