Sparsely substituted chlorins as core constructs in chlorophyll analogue chemistry. II. Derivatization

Tetrahedron. 2007 Apr 30;63(18):3840-3849. doi: 10.1016/j.tet.2007.02.076.

Abstract

Stable chlorins bearing few or no substituents have been subjected to a variety of reactions including demetalation, magnesium insertion, oxochlorin formation, and bromination followed by Suzuki coupling. The kinetics of deuteration also have been determined for two oxochlorins and a series of chlorins bearing 0, 1, 2, or 3 meso-aryl substituents.