Abstract
A trans-chelating chiral bisphosphine, PhTRAP, allows the ruthenium-catalyzed hydrogenation of various azoles to proceed with high enantioselectivity. The PhTRAP-ruthenium catalyst transformed indoles, pyrroles, imidazoles, and oxazoles into the corresponding chiral heterocycles. Naphthalenes are also reduced with hydrogen by the chiral ruthenium catalyst, exclusively giving tetralins. Some 2-alkoxytetralins were obtained with over 90% ee from the catalytic asymmetric hydrogenation of the corresponding substituted naphthalenes.
Original language | English |
---|---|
Pages (from-to) | 715-719 |
Number of pages | 5 |
Journal | Phosphorus, Sulfur and Silicon and the Related Elements |
Volume | 190 |
Issue number | 5-6 |
DOIs | |
Publication status | Published - Jun 3 2015 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Organic Chemistry
- Inorganic Chemistry