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Iron-Catalyzed Cycloisomerization and C−C Bond Activation to Access Non-canonical Tricyclic Cyclobutanes: In memory of Professor Klaus Hafner

Cycloisomerizations are powerful skeletal rearrangements that allow the construction of complex molecular architectures in an atom-economic way. We present here an unusual type of cyclopropyl enyne cycloisomerization that couples the process of a cycloisomerization with the activation of a C−C bond in cyclopropanes. A set of substituted non-canonical tricyclic cyclobutanes were synthesized under mild conditions using [(Ph₃P)₂Fe(CO)(NO)]BF₄ as catalyst in good to excellent yields with high levels of stereocontrol.

Identiferoai:union.ndltd.org:DRESDEN/oai:qucosa:de:qucosa:91598
Date06 June 2024
CreatorsKramm, Frederik, Ullwer, Franziska, Klinnert, Benedict, Zheng, Min, Plietker, Bernd
PublisherWiley-VCH
Source SetsHochschulschriftenserver (HSSS) der SLUB Dresden
LanguageEnglish
Detected LanguageEnglish
Typeinfo:eu-repo/semantics/publishedVersion, doc-type:article, info:eu-repo/semantics/article, doc-type:Text
Rightsinfo:eu-repo/semantics/openAccess
Relation1521-3757, e202205169, 10.1002/anie.202205169, info:eu-repo/grantAgreement/Deutsche Forschungsgemeinschaft/SFB 1333: Molekulare heterogene Katalyse in definierten, dirigierenden Geometrien/358283783/

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