An Enantioselective Suzuki-Miyaura Coupling To Form Axially Chiral Biphenols
- PMID: 35969692
- PMCID: PMC9434994
- DOI: 10.1021/jacs.2c06529
An Enantioselective Suzuki-Miyaura Coupling To Form Axially Chiral Biphenols
Abstract
Axial chirality features prominently in molecules of biological interest as well as chiral catalyst designs, and atropisomeric 2,2'-biphenols are particularly prevalent. Atroposelective metal-catalyzed cross-coupling is an attractive and modular approach to access enantioenriched biphenols, and yet existing protocols cannot achieve this directly. We address this challenge through the use of enantiopure, sulfonated SPhos (sSPhos), an existing ligand that has until now been used only in racemic form and that derives its chirality from an atropisomeric axis that is introduced through sulfonation. We believe that attractive noncovalent interactions involving the ligand sulfonate group are responsible for the high levels of asymmetric induction that we obtain in the 2,2'-biphenol products of Suzuki-Miyaura coupling, and we have developed a highly practical resolution of sSPhos via diastereomeric salt recrystallization.
Conflict of interest statement
The authors declare no competing financial interest.
Figures
References
-
- Clayden J.; Moran W. J.; Edwards P. J.; LaPlante S. R. The Challenge of Atropisomerism in Drug Discovery. Angew. Chem., Int. Ed. 2009, 48, 6398–6401. 10.1002/anie.200901719. - DOI - PubMed
- LaPlante S. R.; Fader L. D.; Fandrick K. R.; Fandrick D. R.; Hucke O.; Kemper R.; Miller S. P. F.; Edwards P. J. Assessing Atropisomer Axial Chirality in Drug Discovery and Development. J. Med. Chem. 2011, 54, 7005–7022. 10.1021/jm200584g. - DOI - PubMed
- Smyth J. E.; Butler N. M.; Keller P. A. A twist of nature – the significance of atropisomers in biological systems. Nat. Prod. Rep. 2015, 32, 1562–1583. 10.1039/C4NP00121D. - DOI - PubMed
- Toenjes S. T.; Gustafson J. L. Atropisomerism in medicinal chemistry: challenges and opportunities. Future Med. Chem. 2018, 10, 409–422. 10.4155/fmc-2017-0152. - DOI - PMC - PubMed
-
- Cammidge A. N.; Crépy K. V. L. The first asymmetric Suzuki cross-coupling reaction. Chem. Commun. 2000, 1723–1724. 10.1039/b004513f. - DOI
- Yin J.; Buchwald S. L. A Catalytic Asymmetric Suzuki Coupling for the Synthesis of Axially Chiral Biaryl Compounds. J. Am. Chem. Soc. 2000, 122, 12051–12052. 10.1021/ja005622z. - DOI
-
- Hayashi T.; Hayashizaki K.; Kiyoi T.; Ito Y. Asymmetric synthesis catalyzed by chiral ferrocenylphosphine-transition-metal complexes. 6. Practical asymmetric synthesis of 1,1′-binaphthyls via asymmetric cross-coupling with a chiral [(alkoxyalkyl)ferrocenyl]monophosphine/nickel catalyst. J. Am. Chem. Soc. 1988, 110, 8153–8156. 10.1021/ja00232a030. - DOI
-
-
For relevant reviews, see the following:
- Cherney A. H.; Kadunce N. T.; Reisman S. E. Enantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents To Construct C–C Bonds. Chem. Rev. 2015, 115, 9587–9652. 10.1021/acs.chemrev.5b00162. - DOI - PMC - PubMed
- Goetzke F. W.; Van Dijk L.; Fletcher S. P.. Catalytic Asymmetric Suzuki–Miyaura Couplings. In PATAI’S Chemistry of Functional Groups; Wiley, 2019; pp 1–54.
- Cheng J. K.; Xiang S.-H.; Li S.; Ye L.; Tan B. Recent Advances in Catalytic Asymmetric Construction of Atropisomers. Chem. Rev. 2021, 121, 4805–4902. 10.1021/acs.chemrev.0c01306. - DOI - PubMed
- Hedouin G.; Hazra S.; Gallou F.; Handa S. The Catalytic Formation of Atropisomers and Stereocenters via Asymmetric Suzuki–Miyaura Couplings. ACS Catal. 2022, 12, 4918–4937. 10.1021/acscatal.2c00933. - DOI
-
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
