Stereodivergent Hydrogermylations of α‑Trifluoromethylated Alkynes and Their Applications in Cross-Coupling Reactions

The hydrometalation of alkynes with group 14 elements such as tin- or silyl hydrides is a classical transformation in organic synthesis. Strangely, among the group 14 elements, the use of germanium hydrides is rarely seen. Two efficient, stereodivergent, and broadly applicable routes to (Z)- and (E)...

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Veröffentlicht in:Organic letters 2015-04, Vol.17 (7), p.1794-1797
Hauptverfasser: Schweizer, Stéphane, Tresse, Cédric, Bisseret, Philippe, Lalevée, Jacques, Evano, Gwilherm, Blanchard, Nicolas
Format: Artikel
Sprache:eng
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Zusammenfassung:The hydrometalation of alkynes with group 14 elements such as tin- or silyl hydrides is a classical transformation in organic synthesis. Strangely, among the group 14 elements, the use of germanium hydrides is rarely seen. Two efficient, stereodivergent, and broadly applicable routes to (Z)- and (E)-α-CF3-vinylgermanes by regio- and stereoselective hydrogermylation of α-trifluoromethylated alkynes under radical or transition-metal-catalyzed conditions are reported. Furthermore, we demonstrate that the resulting stereodefined fluorinated building blocks are remarkable cross-coupling partners, provided that the vinylgermane is appropriately tuned electronically, as demonstrated by the synthesis of trisubstituted (Z)- and (E)-α-trifluoromethylated alkenes.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.5b00579