Abstract
The reaction of 2,5-dihydro-2-diisopropylamino-1,2-thiaborole (5) with 2 equiv of LDA followed by CH2Cl2 gives 2-(diisopropylamino) -2H-1,2-thiaborin (2c), which has been spectroscopically and structurally characterized. DFT calculations indicate that formally aromatic 2c has a limited π-delocalized bonding in its heterocyclic ring.
Original language | English |
---|---|
Pages (from-to) | 3698-3700 |
Number of pages | 3 |
Journal | Organometallics |
Volume | 30 |
Issue number | 14 |
DOIs | |
Publication status | Published - 25 Jul 2011 |
Externally published | Yes |