Photochemical Cyclopropanation of Cyclooctatetraene and (Poly-)unsaturated Carbocycles.


Journal

Organic letters
ISSN: 1523-7052
Titre abrégé: Org Lett
Pays: United States
ID NLM: 100890393

Informations de publication

Date de publication:
02 Jul 2020
Historique:
pubmed: 20 6 2020
medline: 20 6 2020
entrez: 20 6 2020
Statut: ppublish

Résumé

We report on the use of visible light to conduct carbene-transfer reactions of donor/acceptor diazoalkanes with cyclooctatetraene and polyunsaturated carbocycles to give the corresponding cyclopropanes in excellent yields with excellent stereoselectivities. This photochemical protocol proved to be superior to conventional metal-catalyzed cyclopropanation reactions and now provides platform chemicals containing a cyclic conjugated all-cis triene. The cyclopropane is an important structural feature to prevent 6π electrocyclization. Instead, the triene moiety can now be selectively functionalized in cycloaddition reactions.

Identifiants

pubmed: 32551700
doi: 10.1021/acs.orglett.0c01734
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5126-5130

Auteurs

Yujing Guo (Y)

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, D-52074 Aachen, Germany.

Claire Empel (C)

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, D-52074 Aachen, Germany.

Chao Pei (C)

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, D-52074 Aachen, Germany.

Iuliana Atodiresei (I)

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, D-52074 Aachen, Germany.

Thomas Fallon (T)

Department of Chemistry, The University of Adelaide, Adelaide, South Australia 5005, Australia.

Rene M Koenigs (RM)

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, D-52074 Aachen, Germany.

Classifications MeSH