Enantioselective iron-catalysed O-H bond insertions
- PMID: 20571572
- DOI: 10.1038/nchem.651
Enantioselective iron-catalysed O-H bond insertions
Abstract
The ready availability, low price and environmentally benign character of iron mean that it is an ideal alternative to precious metals in catalysis. Recent growth in the number of iron-catalysed reactions reported reflects an increasing demand for sustainable chemistry. Only a limited number of chiral iron catalysts have been reported and these have, in general, proven less enantioselective than other transition-metal catalysts, thus limiting their appeal. Here, we report that iron complexes of spiro-bisoxazoline ligands are highly efficient catalysts for asymmetric O-H bond insertion reactions. These complexes catalyse insertions into the O-H bond of a wide variety of alcohols and even water, with exceptional enantioselectivities under mild reaction conditions. The selectivities surpass those obtained with other transition-metal catalysts. This study should inspire and encourage the use of iron instead of traditional precious metals in the development of greener catalysts for catalytic asymmetric synthesis.
Similar articles
-
Transition-metal-catalyzed enantioselective heteroatom-hydrogen bond insertion reactions.Acc Chem Res. 2012 Aug 21;45(8):1365-77. doi: 10.1021/ar300051u. Epub 2012 May 31. Acc Chem Res. 2012. PMID: 22651217
-
Iron-, Cobalt-, and Nickel-Catalyzed Asymmetric Transfer Hydrogenation and Asymmetric Hydrogenation of Ketones.Acc Chem Res. 2015 Sep 15;48(9):2587-98. doi: 10.1021/acs.accounts.5b00043. Epub 2015 Aug 24. Acc Chem Res. 2015. PMID: 26301426
-
Bioinspired Manganese and Iron Complexes for Enantioselective Oxidation Reactions: Ligand Design, Catalytic Activity, and Beyond.Acc Chem Res. 2019 Aug 20;52(8):2370-2381. doi: 10.1021/acs.accounts.9b00285. Epub 2019 Jul 23. Acc Chem Res. 2019. PMID: 31333021
-
Synthesis and Application of the Transition Metal Complexes of α-Pyridinyl Alcohols, α-Bipyridinyl Alcohols, α,α'-Pyridinyl Diols and α,α'-Bipyridinyl Diols in Homogeneous Catalysis.Molecules. 2018 Apr 12;23(4):896. doi: 10.3390/molecules23040896. Molecules. 2018. PMID: 29649178 Free PMC article. Review.
-
Enantioselective C-H Functionalization Reactions under Gold Catalysis.Chemistry. 2022 Apr 6;28(20):e202104371. doi: 10.1002/chem.202104371. Epub 2022 Feb 15. Chemistry. 2022. PMID: 35014732 Review.
Cited by
-
Mixture of clopidogrel bisulfate and magnesium oxide tablets reduces clopidogrel dose administered through a feeding tube.J Pharm Health Care Sci. 2021 May 4;7(1):18. doi: 10.1186/s40780-021-00202-1. J Pharm Health Care Sci. 2021. PMID: 33941283 Free PMC article.
-
Chemoselective Cyclopropanation over Carbene Y-H Insertion Catalyzed by an Engineered Carbene Transferase.J Org Chem. 2018 Jul 20;83(14):7480-7490. doi: 10.1021/acs.joc.8b00946. Epub 2018 Jul 6. J Org Chem. 2018. PMID: 29905476 Free PMC article.
-
Blue light-promoted photolysis of aryldiazoacetates.Chem Sci. 2018 May 22;9(22):5112-5118. doi: 10.1039/c8sc01165f. eCollection 2018 Jun 14. Chem Sci. 2018. PMID: 29938043 Free PMC article.
-
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion.ACS Cent Sci. 2016 Nov 23;2(11):778-789. doi: 10.1021/acscentsci.6b00272. Epub 2016 Oct 27. ACS Cent Sci. 2016. PMID: 27981231 Free PMC article. Review.
-
Parallel kinetic resolution of aziridines via chiral phosphoric acid-catalyzed apparent hydrolytic ring-opening.Chem Sci. 2023 Oct 12;14(43):12152-12159. doi: 10.1039/d3sc03899h. eCollection 2023 Nov 8. Chem Sci. 2023. PMID: 37969581 Free PMC article.
References
Publication types
MeSH terms
Substances
Associated data
- PubChem-Substance/92309320
- PubChem-Substance/92309321
- PubChem-Substance/92309322
- PubChem-Substance/92309323
- PubChem-Substance/92309324
- PubChem-Substance/92309325
- PubChem-Substance/92309326
- PubChem-Substance/92309327
- PubChem-Substance/92309328
- PubChem-Substance/92309329
- PubChem-Substance/92309330
- PubChem-Substance/92309331
- PubChem-Substance/92309332
- PubChem-Substance/92309333
- PubChem-Substance/92309334
- PubChem-Substance/92309335
- PubChem-Substance/92309336
- PubChem-Substance/92309337
- PubChem-Substance/92309338
- PubChem-Substance/92309339
- PubChem-Substance/92309340
- PubChem-Substance/92309341
- PubChem-Substance/92309342
- PubChem-Substance/92309343
- PubChem-Substance/92309344
- PubChem-Substance/92309345
- PubChem-Substance/92309346
- PubChem-Substance/92309347
- PubChem-Substance/92309348
- PubChem-Substance/92309349
- PubChem-Substance/92309350
- PubChem-Substance/92309351
- PubChem-Substance/92309352
- PubChem-Substance/92309353
- PubChem-Substance/92309354
- PubChem-Substance/92309355
- PubChem-Substance/92309356
- PubChem-Substance/92309357
- PubChem-Substance/92309358
- PubChem-Substance/92309359
- PubChem-Substance/92309360
- PubChem-Substance/92309361
- PubChem-Substance/92309362
- PubChem-Substance/92309363
- PubChem-Substance/92309364
- PubChem-Substance/92309365
- PubChem-Substance/92309366
- PubChem-Substance/92309367
- PubChem-Substance/92309368
- PubChem-Substance/92309369
- PubChem-Substance/92309370
- PubChem-Substance/92309371
- PubChem-Substance/92309372
- PubChem-Substance/92309373
- PubChem-Substance/92309374
- PubChem-Substance/92309375
- PubChem-Substance/92309376
- PubChem-Substance/92309377
- PubChem-Substance/92309378
- PubChem-Substance/92309379
- PubChem-Substance/92309380
- PubChem-Substance/92309381
- PubChem-Substance/92309382
- PubChem-Substance/92309383
- PubChem-Substance/92309384
- PubChem-Substance/92309385
- PubChem-Substance/92309386
- PubChem-Substance/92309387
- PubChem-Substance/92309388
- PubChem-Substance/92309389
- PubChem-Substance/92309390
- PubChem-Substance/92309391
LinkOut - more resources
Full Text Sources
Medical