Studies on a catalytic version of the Matteson asymmetric homologation reaction
Organic & Biomolecular Chemistry2021Vol. 19(19), pp. 4279–4284
Citations Over Time
Abstract
Studies of a catalytic asymmetric version of the Matteson reaction between dichloromethylboronates and organolithium reagents have been undertaken. From several different chiral catalytic systems studied, only one based on a mannitol derivative has given substantial asymmetric induction close to that previously achieved with a bis(oxazoline) derivative and ytterbium triflate. More detailed study of the latter reaction revealed that fresh ytterbium triflate actually reduced the level of asymmetric induction, while "aged" ytterbium triflate, or a fresh sample that had been treated with water, brought about improved induction. The implications of these findings are discussed.
Related Papers
- → Detritylation with ytterbium triflate(2000)35 cited
- → One-Pot Preparation of Pyranoquinolinones by Ytterbium(III) Trifluoromethanesulfonate-Catalyzed Reactions: Efficient Synthesis of Flindersine, N-Methylflindersine, and Zanthosimuline Natural Products(2001)31 cited
- → Novel C2-symmetric bisoxazolines with a chiral trans-(2R,3R)-diphenylcyclopropane backbone: preparation and application in several enantioselective catalytic reactions(2010)19 cited
- → Mild and Efficient Method for Synthesis of Eaminones Using Ytterbium Triflate as Catalyst(2010)5 cited
- → Highly selective Friede–Crafts monoacylation of ferrocene catalysed by ytterbium(III) triflate(2004)5 cited