A structurally prearranged carbaporphyrin, 22-methyl-m-benziporphyrin, provided the perfect macrocyclic platform to form gold(III) 22-methyl-m-benziporphyrin, which facilitates the specific m-benzene ring contraction yielding gold(III) 21-methyl 21-carbaporphyrin with remarkably high yield.

Download full-text PDF

Source
http://dx.doi.org/10.1002/chem.201604458DOI Listing

Publication Analysis

Top Keywords

goldiii triggered
4
triggered transformations
4
transformations 22-methyl-m-benziporphyrin
4
22-methyl-m-benziporphyrin involving
4
involving effective
4
effective contraction
4
contraction benzene
4
benzene cyclopentadiene
4
cyclopentadiene structurally
4
structurally prearranged
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!