Reactions of 3,3’-Linked Bispyrroles with Carbon Electrophiles
The reactivity of 3,3´-linked bispyrroles, easily accessible by ring-enlargement reactions of donor-acceptor cyclopropanes, towards various carbon electrophiles was investigated. A biscyclopropanated furan, equipped with imines as acceptor units, was converted by rearrangement and subsequent elimination of water to 3,3´-linked bispyrroles. Thereby the nucleophilic 2-position of the pyrroles stayed unsubstituted, thus permitting a further reaction with electrophiles. The heterocycles were reacted with oxalyl chloride to form a new six-membered ring between the pyrrolic subunits. The 1,2-diketone moiety in these species was used as a starting point to extend the π-system via a condensation reaction with aromatic 1,2-diamines. The reaction of 3,3’-linked bispyrroles with the phosgene surrogate triphosgene led to a seven-membered anhydride. The use of the Vilsmeier reagent led to a formylation of the bispyrroles. Furthermore, a direct oxidative coupling between two bispyrroles resulted in a previously unknown linkage (3,3':2',2'':3'',3''') between four pyrrole subunits.
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License Holder: This is the peer reviewed version of the following article: Reactions of 3,3′‐Linked Bispyrroles with Carbon Electrophiles, which has been published in final form at https://doi.org/10.1002/ejoc.201900106. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
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