par Borbas, K Eszter;Ruzié, Christian 
;Lindsey, Jonathan S
Référence Organic letters, 10, 10, page (1931-1934)
Publication Publié, 2008-05
;Lindsey, Jonathan SRéférence Organic letters, 10, 10, page (1931-1934)
Publication Publié, 2008-05
Article révisé par les pairs
| Résumé : | Bacteriochlorins absorb strongly in the near-infrared spectral region and hence are ideally suited for diverse photomedical applications, yet naturally occurring bacteriochlorins have limited stability and synthetic malleability. A de novo route has been exploited to prepare synthetic bacteriochlorins that bear a geminal dimethyl group in each pyrroline ring for stability and a symmetrically branched 1,5-dimethoxypentyl group attached to each pyrrole ring for solubility in lipophilic media. |
