Abstract
Zirconacyclopropenylboronates can be stabilized to dimerization by complexation with tributylphosphine; the phosphine stabilized zirconacycle boronates react with aliphatic and aromatic ketones and aldehydes at C2 of the triple bond to give the previously unknown 3-hydroxyvinylboronates in 61-80% isolated yields.
Original language | English |
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Pages (from-to) | 5589-5591 |
Number of pages | 3 |
Journal | Chemical Communications |
Issue number | 43 |
DOIs | |
State | Published - 2008 |