| Literature DB >> 27709907 |
Satoru Hiroto1, Yoshihiro Miyake1, Hiroshi Shinokubo1.
Abstract
This review focuses on the postfunctionalization of porphyrins and related compounds through catalytic and stoichiometric organometallic methodologies. The employment of organometallic reactions has become common in porphyrin synthesis. Palladium-catalyzed cross-coupling reactions are now standard techniques for constructing carbon-carbon bonds in porphyrin synthesis. In addition, iridium- or palladium-catalyzed direct C-H functionalization of porphyrins is emerging as an efficient way to install various substituents onto porphyrins. Furthermore, the copper-mediated Huisgen cycloaddition reaction has become a frequent strategy to incorporate porphyrin units into functional molecules. The use of these organometallic techniques, along with the traditional porphyrin synthesis, now allows chemists to construct a wide range of highly elaborated and complex porphyrin architectures.Entities:
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Year: 2016 PMID: 27709907 DOI: 10.1021/acs.chemrev.6b00427
Source DB: PubMed Journal: Chem Rev ISSN: 0009-2665 Impact factor: 60.622