meso-Aryl-Substituted Expanded Porphyrins-Reference-Cited by-同舟云学术

meso-Aryl-Substituted Expanded Porphyrins

Published:2001-06-29 Issue:29 Volume:123 Page:7190-7191
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Shin Ji-Young¹,Furuta Hiroyuki¹,Yoza Kenji¹,Igarashi Shinetsu¹,Osuka Atsuhiro¹

Affiliation:

1. Department of Chemistry, Graduate School of Science Kyoto University, Kyoto 606-8502, Japan Bruker Japan, Tsukuba, Ibaraki 305-0051, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0106624

Reference15 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. Giant Porphyrinoids: From Figure Eights to Nanomolecular Cavities

3. Synthesis of [28]Heptaphyrin(1.0.0.1.0.0.0) and [32]Octaphyrin(1.0.0.0.1.0.0.0) via a Directed Oxidative Ring Closure: The First Expanded Porphyrins Containing a Quaterpyrrole Subunit

4. 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)

5. 5,10,15-Triphenylcorrole: a product from a modified Rothemund reaction

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