| Literature DB >> 17602489 |
Timothy D Lash1, Komal Pokharel, Jill M Serling, Valerie R Yant, Gregory M Ferrence.
Abstract
Pyriporphyrins with three different orientations for the pyridine moiety have been prepared using a '3 + 1' strategy. The nonaromatic pyriporphyrins are stable so long as phenyl substituents are present at the meso-positions adjacent to the pyridine ring. An aromatic dihydropyriporphyrin with an external CO2Ph protective group has also been prepared from 2,4-pyridinedicarbaldehyde.Entities:
Year: 2007 PMID: 17602489 DOI: 10.1021/ol071052x
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005