Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5289620 | Tetrahedron Letters | 2006 | 4 Pages |
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
Authors
Júlio S. Rebouças, Brian R. James,