Carbene-mediated stereoselective olefination of vinyl sulfoxonium ylides with diazo compounds and acetals

The development of stereoselective olefination using sulfur ylide-derived vinyl carbenes with diazo esters and acetals is reported. Both reactions proceed through nucleophilic addition to electrophiles at the γ-position of an in situ-generated 2-alkoxy furan intermediate. The synthetic utility of the developed method is demonstrated by the total synthesis of rubrolide E. Detailed mechanistic investigations and quantum chemical calculations provide insight into the reaction mechanism.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:60

Enthalten in:

Chemical communications (Cambridge, England) - 60(2024), 28 vom: 02. Apr., Seite 3846-3849

Sprache:

Englisch

Beteiligte Personen:

Gopalakrishnan, Dinesh Kumar [VerfasserIn]
Bhardwaj, Srashti [VerfasserIn]
Kumar, Sandeep [VerfasserIn]
Karmakar, Tarak [VerfasserIn]
Vaitla, Janakiram [VerfasserIn]

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Journal Article

Anmerkungen:

Date Revised 02.04.2024

published: Electronic

Citation Status PubMed-not-MEDLINE

doi:

10.1039/d4cc00450g

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM369870093