posted on 2011-07-25, 00:00authored byAhleah D. Rohr, Mark M. Banaszak Holl, Jeff W. Kampf, Arthur J. Ashe
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.