z-logo
Premium
A Rhodium‐Mediated Contraction of Benzene to Cyclopentadiene: Transformations of Rhodium(III) m ‐Benziporphyrin
Author(s) -
Hurej Karolina,
Pawlicki Miłosz,
Szterenberg Ludmiła,
LatosGrażyński Lechosław
Publication year - 2016
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201508033
Subject(s) - rhodium , chemistry , cyclopentadiene , benzene , carbon atom , contraction (grammar) , phenylene , stereochemistry , catalysis , organic chemistry , polymer , medicine , alkyl
The contraction of benzene is one of an exclusive group of reactions where the cleavage of aromatic structure is of fundamental importance. Rhodium(III) m ‐benziporphyrin undergoes an unprecedented transformation of the built‐in m ‐phenylene in which a perimeter carbon atom is extruded to form rhodium(III) 21‐carbaporphyrin, stabilizing the formyl‐unit‐substituted rhodacyclopropane motif.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here