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Abstract A gold(I)‐catalyzed enantioselective dearomatization is achieved via metal‐chiral ligand cooperation. A new and divergent synthesis of chiral bifunctional binaphthyl‐2‐ylphosphines is developed to allow rapid access to these ligands, which in turn facilitate the application of this chemistry to a broad substrate scope including 1‐naphthols, 2‐naphthols, and phenols. Enantiomeric excesses up to 98 % are achieved via selective acceleration of one enantiomer formation enabled by hydrogen bonding between substrate and ligand remote basic group. DFT calculations lend support to the cooperative catalysis and substantiate the reaction stereochemical outcomes.
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Interplay of Computation and Experiment in Enantioselective Catalysis: Rationalization, Prediction, and─Correction?
The application of computational methods in enantioselective catalysis has evolved from the rationalization of the observed stereochemical outcome to their prediction and application to the design of chiral ligands. This Perspective provides an overview of the current methods used, ranging from atomistic modeling of the transition structures involved to correlation-based methods with particular emphasis placed on the Q2MM/CatVS method. Using three enantioselective palladium-catalyzed reactions, namely, the conjugate addition of arylboronic acids to enones, the enantioselective redox relay Heck reaction, and the Tsuji–Trost allylic amination as case studies, we argue that computational methods have become truly equal partners to experimental studies in that, in some cases, they are able to correct published stereochemical assignments. Finally, the consequences of this approach to data-driven methods are discussed.
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- PAR ID:
- 10472723
- Publisher / Repository:
- American Chemical Society
- Date Published:
- Journal Name:
- ACS Catalysis
- Volume:
- 13
- Issue:
- 21
- ISSN:
- 2155-5435
- Page Range / eLocation ID:
- 14285 to 14299
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1021/acscatal.3c03921
