The 1,1-Carboboration of Bis(alkynyl)phosphanes as a Route to Phosphole Compounds

Neat and tidy: B(C6F5)3 efficiently converts a series of bis(alkynyl)phosphanes into highly substituted 3‐borylphospholes through a twofold 1,1‐carboboration reaction sequence. The boron substituted phospholes were also used as substrates in Suzuki–Miyaura type cross‐coupling reactions (see scheme)....

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Veröffentlicht in:Angewandte Chemie International Edition 2012-02, Vol.51 (8), p.1954-1957
Hauptverfasser: Möbus, Juri, Bonnin, Quentin, Ueda, Kirika, Fröhlich, Roland, Itami, Kenichiro, Kehr, Gerald, Erker, Gerhard
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container_end_page 1957
container_issue 8
container_start_page 1954
container_title Angewandte Chemie International Edition
container_volume 51
creator Möbus, Juri
Bonnin, Quentin
Ueda, Kirika
Fröhlich, Roland
Itami, Kenichiro
Kehr, Gerald
Erker, Gerhard
description Neat and tidy: B(C6F5)3 efficiently converts a series of bis(alkynyl)phosphanes into highly substituted 3‐borylphospholes through a twofold 1,1‐carboboration reaction sequence. The boron substituted phospholes were also used as substrates in Suzuki–Miyaura type cross‐coupling reactions (see scheme).
doi_str_mv 10.1002/anie.201107398
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1521-3773
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source Wiley Journals
subjects boranes
Boron
carboboration
cross-coupling
phospholes
Sequences
Series (mathematics)
title The 1,1-Carboboration of Bis(alkynyl)phosphanes as a Route to Phosphole Compounds
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