5, 10-Diphenyltripyrrane, a useful building block for the synthesis of meso-phenyl substituted expanded macrocycles
…, ED Sternberg, RW Boyle, D Dolphin
Index: Brueckner, Christian; Sternberg, Ethan D.; Boyle, Ross W.; Dolphin, David Chemical Communications, 1997 , # 17 p. 1689 - 1690
Full Text: HTML
Citation Number: 59
Abstract
Pyrrole and benzaldehyde were condensed under acidic conditions to produce a mixture of 5-phenyldipyrromethane and 5, 10-diphenyltripyrrane; the tripyrrane was utilized in syntheses of meso-phenylsapphyrins, meso-diphenylpentaphyrin and meso- hexaphenylhexaphyrin.
Related Articles:
New polyethyleneglycol-functionalized texaphyrins: synthesis and in vitro biological studies
[Wei, Wen-Hao; Wang, Zhong; Mizuno, Toshihisa; Cortez, Cecilia; Fu, Lei; Sirisawad, Mint; Naumovski, Louie; Magda, Darren; Sessler, Jonathan L. Dalton Transactions, 2006 , # 16 p. 1934 - 1942]
Effective meso Fabrications of Subporphyrins
[Kitano, Masaaki; Hayashi, Shin-Ya; Tanaka, Takayuki; Yorimitsu, Hideki; Aratani, Naoki; Osuka, Atsuhiro Angewandte Chemie - International Edition, 2012 , vol. 51, # 23 p. 5593 - 5597]
Effective meso Fabrications of Subporphyrins
[Kitano, Masaaki; Hayashi, Shin-Ya; Tanaka, Takayuki; Yorimitsu, Hideki; Aratani, Naoki; Osuka, Atsuhiro Angewandte Chemie - International Edition, 2012 , vol. 51, # 23 p. 5593 - 5597]
Effective meso Fabrications of Subporphyrins
[Kitano, Masaaki; Hayashi, Shin-Ya; Tanaka, Takayuki; Yorimitsu, Hideki; Aratani, Naoki; Osuka, Atsuhiro Angewandte Chemie - International Edition, 2012 , vol. 51, # 23 p. 5593 - 5597]
[Nielsen, Kent A.; Levillain, Eric; Lynch, Vincent M.; Sessler, Jonathan L.; Jeppesen, Jan O. Chemistry - A European Journal, 2009 , vol. 15, # 2 p. 506 - 516]