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An Ir/Zn Dual Catalysis for Enantio- and Diastereodivergent α‑Allylation of α‑Hydroxyketones
Abstract
An Ir/Zn dual catalysis has been developed for the enantio- and diastereodivergent α-allylation of unprotected α-hydroxyketones under mild conditions, in the absence of any additional base. The cooperative action of a chiral iridium complex derived from phosphoramidites and a chiral Zn-ProPhenol complex is most likely responsible for its high reactivity, excellent enantioselectivity (up to >99% ee), and good diastereoselectivity (up to >20:1 dr). All four product stereoisomers could be prepared from the same set of starting materials and under identical conditions by simple selection of appropriate catalyst combinations- Text
- Journal contribution
- Biochemistry
- Medicine
- Genetics
- Evolutionary Biology
- Sociology
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- Developmental Biology
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- Environmental Sciences not elsewhere classified
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- enantioselectivity
- chiral iridium
- diastereodivergent α- allylation
- diastereoselectivity
- Enantio
- product stereoisomers
- chiral Zn-ProPhenol
- material
- Catalysi
- enantio
- ee
- absence
- Hydroxyketone
- catalysi
- Allylation
- α- hydroxyketones
- Diastereodivergent
- catalyst combinations
- Ir
- reactivity
- phosphoramidite