Improved Synthesis of meso-Aryl-Substituted [26]Hexaphyrins
Author:
Affiliation:
1. Department of Chemistry, Graduate School of Science, Kyoto University, and CREST (Core Research for Evolutional Science and Technology) of Japan Science and Technology Corporation (JST), Sakyo-ku, Kyoto 606-8502, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol035650x
Reference19 articles.
1. Sessler, J. L.; Gebauer, A.; Weghorn, S. J. InThe PorphyrinHandbook; Kadish, K. M., Smith, K. M.,Guilard, R., Eds.; Academic Press: San Diego, 1999; Vol. 2, pp 55−124.
2. Expanded Porphyrins and Their Heterologs
3. Bis(azafulvene) as a Versatile Building Block for Giant Cyclopolypyrroles: X-ray Crystal Structure of [64]Hexadecaphyrin(1.0.1.0.1.0.1.0.1.0.1.0.1.0.1.0)
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