Abstract
Oxidative addition of the C-O bond in L2PhB: (L=oxazol-2-ylidene) to an AlI center induced ring expansion of an oxazol-2-ylidene ring, affording a unique organoboron species formally involving either an Al, N, O mixed heterocyclic carbene or anionic (amino)(boryl)carbene fragment. Ring expansion of an oxazol-2-ylidene in L2PhB (L=oxazol-2-ylidene) through cleavage of the C-O bond by AlI resulted in the formation of a unique organoboron species formally involving either an Al, N, O mixed heterocyclic carbene or an anionic (amino)(boryl)carbene fragment.
Original language | English |
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Pages (from-to) | 1922-1925 |
Number of pages | 4 |
Journal | Chemistry - A European Journal |
Volume | 22 |
Issue number | 6 |
DOIs | |
Publication status | Published - Feb 5 2016 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
ASJC Scopus Subject Areas
- Catalysis
- General Chemistry
- Organic Chemistry
Keywords
- aluminum
- carbenes
- density functional calculations
- oxidative addition
- ring expansion