Speck M, Senge MO, Schäfer A, Kurreck H (1997)
Publication Type: Journal article, Original article
Publication year: 1997
Original Authors: Speck M., Senge M., Schäfer A., Kurreck H.
Publisher: Elsevier
Book Volume: 7
Pages Range: 2589-2592
Journal Issue: 20
DOI: 10.1016/S0960-894X(97)10027-0
Porphyrin quinones with sterically demanding 3,6-di-tert-butyl-o-quinones were synthesized for electron transfer studies. In the presence of atmospheric oxygen the covalently free base porphyrin-o-quinones are oxidized to muconic acid anhydride and 3,6-dicarbonyl-derivatives. In contrast to the well established chemistry of catecholase models based on 3,5-substituted quinones this is die first example for oxidative ring expansion of 3,6-disubstituted o-quinones.
APA:
Speck, M., Senge, M.O., Schäfer, A., & Kurreck, H. (1997). Novel oxidation reactions of sterically demanding 3,6-di-tert-butyl porphyrin-o-quinones to muconic anhydride derivatives. Bioorganic & Medicinal Chemistry Letters, 7(20), 2589-2592. https://dx.doi.org/10.1016/S0960-894X(97)10027-0
MLA:
Speck, Marcus, et al. "Novel oxidation reactions of sterically demanding 3,6-di-tert-butyl porphyrin-o-quinones to muconic anhydride derivatives." Bioorganic & Medicinal Chemistry Letters 7.20 (1997): 2589-2592.
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