Reaction Mechanism of a Nonheme Iron Enzyme Catalyzed Oxidative Cyclization via C-C Bond Formation.


Journal

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

Informations de publication

Date de publication:
04 01 2019
Historique:
pubmed: 15 12 2018
medline: 16 7 2019
entrez: 15 12 2018
Statut: ppublish

Résumé

A complementary study including design of mechanistic probes, biochemical assays, model analysis, and liquid chromatography coupled mass spectrometry was conducted to establish the reaction mechanism for a nonheme iron enzyme catalyzed (-)-podophyllotoxin formation. Our results indicate that the originally proposed hydroxylated intermediate is unlikely to be involved in this reaction. Instead, the formation of benzylic radical/carbocation intermediate can be utilized to trigger the C-C bond formation to construct the C-ring of (-)-podophyllotoxin.

Identifiants

pubmed: 30550285
doi: 10.1021/acs.orglett.8b03670
doi:

Substances chimiques

Nonheme Iron Proteins 0
Podophyllotoxin L36H50F353

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

228-232

Auteurs

Wei-Chen Chang (WC)

Department of Chemistry , North Carolina State University , Raleigh , North Carolina 27695 , United States.

Zhi-Jie Yang (ZJ)

Department of Chemistry , National Taiwan Normal University , Taipei 11677 , Taiwan.

Yueh-Hua Tu (YH)

Department of Chemistry , National Taiwan Normal University , Taipei 11677 , Taiwan.

Tun-Cheng Chien (TC)

Department of Chemistry , National Taiwan Normal University , Taipei 11677 , Taiwan.

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Classifications MeSH