Cobalt-Catalyzed Hydroacylative Dimerization of Allenes Leading to Skipped Dienes

A cobalt–diphosphine catalyst has been found to promote a selective 1:2 coupling reaction between aldehydes and allenes to form β,δ-dialkylidene ketones, featuring skipped diene moieties, with high regioselectivities and stereoselectivities. The reaction is distinct from previously reported, rhodium...

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Veröffentlicht in:Organic letters 2019-08, Vol.21 (15), p.6173-6178
Hauptverfasser: Ding, Wei, Ho, Yan King Terence, Okuda, Yasuhiro, Wijaya, Christopher Kevin, Tan, Zheng Hao, Yoshikai, Naohiko
Format: Artikel
Sprache:eng
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Zusammenfassung:A cobalt–diphosphine catalyst has been found to promote a selective 1:2 coupling reaction between aldehydes and allenes to form β,δ-dialkylidene ketones, featuring skipped diene moieties, with high regioselectivities and stereoselectivities. The reaction is distinct from previously reported, rhodium-catalyzed aldehyde–allene 1:2 coupling to afford β,γ-dialkylidene ketones bearing 1,3-diene moieties. The present hydroacylative dimerization involves a unique allene/allene oxidative cyclization mode to form a C1–C2 linkage between the allene molecules.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.9b02465