Synthesis of P‑Stereogenic Benzoazaphosphole 1‑Oxides via Alkynylation of P‑Stereogenic ortho-Aurated and ortho-Iodo Phosphinic Amides

An efficient methodology for the synthesis of P-stereogenic dihydrobenzoazaphosphole 1-oxides via intramolecular 5-exo-dig alkyne hydroamination promoted by tetrabutylammonium fluoride is herein described. The required chiral o-alkynylphosphinic amide starting materials were prepared in high yields...

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Veröffentlicht in:ACS omega 2018-05, Vol.3 (5), p.5116-5124
Hauptverfasser: Soengas, Raquel, Belmonte Sánchez, Eva, Iglesias, María José, López Ortiz, Fernando
Format: Artikel
Sprache:eng
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Zusammenfassung:An efficient methodology for the synthesis of P-stereogenic dihydrobenzoazaphosphole 1-oxides via intramolecular 5-exo-dig alkyne hydroamination promoted by tetrabutylammonium fluoride is herein described. The required chiral o-alkynylphosphinic amide starting materials were prepared in high yields under very mild reaction conditions through alkynylation of P-stereogenic (O^C)-cyclometalated (phosphinic amide)­dichlorogold­(III) complexes and Sonogashira cross-coupling of ortho-iodo P-stereogenic phosphinic amide.
ISSN:2470-1343
2470-1343
DOI:10.1021/acsomega.8b00491