Asymmetric Hydroboration of Ketones by Cooperative Lewis Acid–Onium Salt Catalysis: A Quantum Chemical and Microkinetic Study to Combine Theory and Experiment-Reference-Cited by-同舟云学术

Asymmetric Hydroboration of Ketones by Cooperative Lewis Acid–Onium Salt Catalysis: A Quantum Chemical and Microkinetic Study to Combine Theory and Experiment

Published:2022-01-10 Issue:2 Volume:12 Page:1497-1507
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Heitkämper Juliane¹,Herrmann Justin²,Titze Marvin²,Bauch Soeren M.¹,Peters René²^ORCID,Kästner Johannes¹^ORCID

Affiliation:

1. Institute for Theoretical Chemistry, University of Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany

2. Institute of Organic Chemistry, University of Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany

Funder

Deutsche Forschungsgemeinschaft

Studienstiftung des Deutschen Volkes

State of Baden-W ?urttemberg

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.1c05440

Reference57 articles.

1. Highly Active Cooperative Lewis Acid—Ammonium Salt Catalyst for the Enantioselective Hydroboration of Ketones

2. Contact Ion Pair Directed Lewis Acid Catalysis: Asymmetric Synthesis oftrans‐Configured β‐Lactones

3. Catalytic Asymmetric Synthesis of trans-Configured β-Lactones: Cooperation of Lewis Acid and Ion Pair Catalysis

4. Cooperative Al(Salen)-Pyridinium Catalysts for the Asymmetric Synthesis of trans-Configured β-Lactones by [2+2]-Cyclocondensation of Acylbromides and Aldehydes: Investigation of Pyridinium Substituent Effects

5. Cooperative Lewis acid–onium salt catalysis as tool for the desymmetrization of meso-epoxides

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