Abstract
Asymmetric synthesis of tetrahydrobenzodiazepines was achieved by transfer hydrogenation of dihydrobenzodiazepines with benzothiazoline having a hydrogen-bonding donor substituent by means of a newly synthesized chiral phosphoric acid. This method was applicable to various racemic dihydrobenzodiazepines to give the corresponding products in good yields with excellent diastereoselectivities and enantioselectivities taking advantage of the dynamic kinetic resolution. Furthermore, the effect of bulky substituent at 3,3′-position on the catalyst and hydrogen-bonding donor substituent on benzothiazoline was fully elucidated by the theoretical study.
Original language | English |
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Pages (from-to) | 8078-8083 |
Number of pages | 6 |
Journal | Chemistry - A European Journal |
Volume | 22 |
Issue number | 24 |
DOIs | |
Publication status | Published - 2016 Jun 6 |
Keywords
- dynamic kinetic resolution
- heterocycles
- hydrogenation
- organocatalysis
- stereoselective synthesis
ASJC Scopus subject areas
- Catalysis
- Organic Chemistry