Screening for generality in asymmetric catalysis.


Journal

Nature
ISSN: 1476-4687
Titre abrégé: Nature
Pays: England
ID NLM: 0410462

Informations de publication

Date de publication:
10 2022
Historique:
received: 09 05 2022
accepted: 22 08 2022
pubmed: 2 9 2022
medline: 29 10 2022
entrez: 1 9 2022
Statut: ppublish

Résumé

Research in the field of asymmetric catalysis over the past half century has resulted in landmark advances, enabling the efficient synthesis of chiral building blocks, pharmaceuticals and natural products

Identifiants

pubmed: 36049504
doi: 10.1038/s41586-022-05263-2
pii: 10.1038/s41586-022-05263-2
pmc: PMC9645431
mid: NIHMS1847251
doi:

Substances chimiques

Biological Products 0
Pharmaceutical Preparations 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

680-686

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM043214
Pays : United States
Organisme : NIGMS NIH HHS
ID : R37 GM043214
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Nature Limited.

Références

Knowles, W. S., Sabacky, M. J. & Büthe, H. Catalytic asymmetric hydrogenation employing a soluble, optically active, rhodium complex. Chem. Commun. (London) 1445–1446 (1968).
Horner, L., Siegel, H. & Büthe, H. Asymmetric catalytic hydrogenation with an optically active phosphine–rhodium complex in homogeneous solution. Angew. Chem. Int. Ed. 7, 942 (1968).
doi: 10.1002/anie.196809422
Jacobsen, E. N., Pfaltz, A. & Yamamoto, H. (eds) Comprehensive Asymmetric Catalysis Vols. 1–3 (Springer, 1999).
Katsuki, T. & Sharpless, K. B. The first practical method for asymmetric epoxidation. J. Am. Chem. Soc. 102, 5974–5976 (1980).
doi: 10.1021/ja00538a077
Jacobsen, E. N., Marko, I., Mungall, W. S., Schroeder, G. & Sharpless, K. B. Asymmetric dihydroxylation via ligand-accelerated catalysis. J. Am. Chem. Soc. 110, 1968–1970 (1988).
doi: 10.1021/ja00214a053
Noyori, R. et al. Asymmetric hydrogenation of β-keto carboxylic esters. A practical, purely chemical access to β-hydroxy esters in high enantiomeric purity. J. Am. Chem. Soc. 109, 5856–5858 (1989).
doi: 10.1021/ja00253a051
Hirao, A., Itsuno, S., Nakahama, S. & Yamazaki, N. Asymmetric reduction of aromatic ketones with chiral alkoxy-amineborane complexes. J. Chem. Soc. Chem. Commun. 315–317 (1981).
Tokunaga, M., Larrow, J. F., Kakiuchi, F. & Jacobsen, E. N. Asymmetric catalysis with water: efficient kinetic resolution of terminal epoxides by means of catalytic hydrolysis. Science 277, 936–938 (1997).
pubmed: 9252321 doi: 10.1126/science.277.5328.936
Schmidt-Dannert, C. & Arnold, F. H. Directed evolution of industrial enzymes. Trends Biotechnol. 17, 135–136 (1999).
pubmed: 10203769 doi: 10.1016/S0167-7799(98)01283-9
Gao, X. & Kagan, H. B. One-pot multi-substrate screening in asymmetric catalysis. Chirality 10, 120–124 (1998).
doi: 10.1002/chir.19
Satyanarayana, T. & Kagan, H. B. The multi-substrate screening of asymmetric catalysis. Adv. Synth. Catal. 347, 737–748 (2005).
doi: 10.1002/adsc.200505057
Kim, H. et al. A multi-substrate screening approach for the identification of a broadly applicable Diels–Alder catalyst. Nat. Commun. 10, 770 (2019).
pubmed: 30770804 pmcid: 6377681 doi: 10.1038/s41467-019-08374-z
Prieto Kullmer, C. N. et al. Accelerating reaction generality and mechanistic insight through additive mapping. Science 376, 532–539 (2022).
pubmed: 35482871 doi: 10.1126/science.abn1885
You, L., Zha, D. & Ansyln, E. V. Recent advances in supramolecular analytical chemistry using optical sensing. Chem. Rev. 115, 7840–7892 (2015).
pubmed: 25719867 doi: 10.1021/cr5005524
Herrera, B. T., Pilicer, S. L., Ansyln, E. V., Joyce, L. A. & Wolf, C. Optical analysis of reaction yield and enantiomeric excess. A new paradigm ready for prime time. J. Am. Chem. Soc. 140, 10385–10401 (2018).
pubmed: 30059621 doi: 10.1021/jacs.8b06607
Jang, S. & Kim, H. Direct chiral
pubmed: 32910666 doi: 10.1021/acs.orglett.0c02620
Feagin, T. A., Olsen, D. P. V., Headman, Z. C. & Heemstra, J. M. High-throughput enantiopurity analysis using enantiomeric DNA-based sensors. J. Am. Chem. Soc. 137, 4198–4206 (2015).
pubmed: 25747268 doi: 10.1021/jacs.5b00923
Guo, J., Wu, J., Siuzdak, G. & Finn, M. G. Measurement of enantiomeric excess by kinetic resolution and mass spectrometry. Angew. Chem. Int. Ed. 38, 1755–1758 (1999).
doi: 10.1002/(SICI)1521-3773(19990614)38:12<1755::AID-ANIE1755>3.0.CO;2-Q
Reetz, M. T., Becker, M. H., Klein, H.-W. & Stöckigt, D. A method for high-throughput screening of enantioselective catalysts. Angew. Chem. Int. Ed. 38, 1758–1761 (1999).
doi: 10.1002/(SICI)1521-3773(19990614)38:12<1758::AID-ANIE1758>3.0.CO;2-8
Abato, P. & Seto, C. T. EMDee: an enzymatic method for determining enantiomeric excess. J. Am. Chem. Soc. 123, 9206–9207 (2001).
pubmed: 11552847 doi: 10.1021/ja016177q
Zhao, Y., Woo, G., Thomas, S., Semin, D. & Sandra, P. Rapid method development for chiral separation in drug discovery using sample pooling and supercritical fluid chromatography–mass spectrometry. J. Chrom. A 1003, 157–166 (2003).
doi: 10.1016/S0021-9673(03)00725-8
Barhate, C. L. et al. Ultrafast chiral separations for high throughput enantiopurity analysis. Chem. Commun. 53, 509–512 (2017).
doi: 10.1039/C6CC08512A
Shen, J., Ikai, T. & Okamoto, Y. Synthesis and application of immobilized polysaccharide-based chiral stationary phases for enantioseparation by high-performance liquid chromatography. J. Chromatogr. A 1363, 51–61 (2014).
pubmed: 24997110 doi: 10.1016/j.chroma.2014.06.042
Korch, K. M. et al. Selected ion monitoring using low-cost mass spectrum detectors provides a rapid, general, and accurate method for enantiomeric excess determination in high-throughput experimentation. ACS Catal. 12, 6737–6745 (2022).
doi: 10.1021/acscatal.2c01628
Payne, C. & Kass, S. R. How reliable are enantiomeric excess measurements obtained by chiral HPLC? ChemistrySelect 5, 1810–1817 (2020).
doi: 10.1002/slct.202000166
Annesley, T. Ion suppression in mass spectrometry. Clin. Chem. 49, 1041–1044 (2003).
pubmed: 12816898 doi: 10.1373/49.7.1041
George, R. et al. Enhancement and suppression of ionization in drug analysis using HPLC-MS/MS in support of therapeutic drug monitoring: a review of current knowledge of its minimization and assessment. Ther. Drug. Monit. 40, 1–8 (2018).
pubmed: 29240615 doi: 10.1097/FTD.0000000000000471
Cox, E. D. & Cook, J. M. The Pictet-Spengler condensation: a new direction for an old reaction. Chem. Rev. 95, 1797–1842 (1995).
doi: 10.1021/cr00038a004
Stöckigt, J., Antonchick, A. P., Wu, F. & Walmann, H. The Pictet–Spengler reaction in nature and in organic chemistry. Angew. Chem. Int. Ed. 50, 8538–8564 (2011).
doi: 10.1002/anie.201008071
Taylor, M. S. & Jacobsen, E. N. Highly enantioselective catalytic acyl-Pictet–Spengler reactions. J. Am. Chem. Soc. 126, 10558–10559 (2004).
pubmed: 15327311 doi: 10.1021/ja046259p
Seayad, J., Seayad, A. M. & List, B. Catalytic asymmetric Pictet–Spengler reaction. J. Am. Chem. Soc. 128, 1086–1087 (2006).
pubmed: 16433519 doi: 10.1021/ja057444l
Wanner, M. J., van der Haas, R. N. S., de Cuba, K. R., van Maarseveen, J. H. & Hiemstra, H. Catalytic asymmetric Pictet–Spengler reactions via sulfenyliminium ions. Angew. Chem. Int. Ed. 46, 7485–7487 (2007).
doi: 10.1002/anie.200701808
Raheem, I. T., Thiara, P. V., Peterson, E. A. & Jacobsen, E. N. Enantioselective Pictet–Spengler-type cyclizations of hydroxylactams: H-bond donor catalysis by anion binding. J. Am. Chem. Soc. 129, 13404–13405 (2007).
pubmed: 17941641 doi: 10.1021/ja076179w
Sewgobind, N. V. et al. Enantioselective BINOL-phosphoric acid catalyzed Pictet−Spengler reactions of N-benzyltryptamine. J. Org. Chem. 73, 6405–6408 (2008).
pubmed: 18616320 doi: 10.1021/jo8010478
Huang, D., Xu, F., Lin, X. & Wang, Y. Highly enantioselective Pictet–Spengler reaction catalyzed by SPINOL‐phosphoric acids. Chem. Eur. J. 18, 3148–3152 (2012).
pubmed: 22354859 doi: 10.1002/chem.201103207
Mittal, N., Sun, D. X. & Seidel, D. Conjugate-base-stabilized Brønsted acids: catalytic enantioselective Pictet–Spengler reactions with unmodified tryptamine. Org. Lett. 16, 1012–1015 (2014).
pubmed: 24446703 doi: 10.1021/ol403773a
Qi, L., Hou, H., Ling, F. & Zhong, W. The cinchona alkaloid squaramide catalyzed asymmetric Pictet–Spengler reaction and related theoretical studies. Org. Biomol. Chem. 16, 566–574 (2018).
pubmed: 29292461 doi: 10.1039/C7OB02606D
Glinsky-Olivier, N., Yang, S., Retailleau, P., Gandon, V. & Guinchard, X. Enantioselective gold-catalyzed Pictet–Spengler reaction. Org. Lett. 21, 9446–9451 (2019).
pubmed: 31725302 doi: 10.1021/acs.orglett.9b03656
Kondo, M. et al. Practical stereoselective synthesis of C3‐spirooxindole‐ and C2‐spiropseudoindoxyl‐pyrrolidines via organocatalyzed Pictet‐Spengler reaction/oxidative rearrangement sequence. Adv. Synth. Catal. 363, 2648–2663 (2021).
doi: 10.1002/adsc.202001472
Lynch-Colameta, T., Greta, S. & Snyder, S. A. Synthesis of aza-quaternary centers via Pictet–Spengler reactions of ketonitrones. Chem. Sci. 12, 6181–6187 (2021).
pubmed: 33996016 pmcid: 8098696 doi: 10.1039/D1SC00882J
Muratore, M. E. et al. Enantioselective Brønsted acid-catalyzed N-acyliminium cyclization cascades. J. Am. Chem. Soc. 131, 10796–10797 (2009).
pubmed: 19606900 doi: 10.1021/ja9024885
Klausen, R. S. & Jacobsen, E. N. Weak Brønsted acid-thiourea co-catalysis: enantioselective, catalytic protio-Pictet-Spengler reactions. Org. Lett. 11, 887–890 (2009).
pubmed: 19178157 pmcid: 2664157 doi: 10.1021/ol802887h
Nakamura, S., Matsuda, Y., Takehara, T. & Suzuki, T. Enantioselective Pictet−Spengler reaction of acyclic α‐ketoesters using chiral imidazoline-phosphoric acid catalysts. Org. Lett. 24, 1072–1076 (2022).
pubmed: 35080408 doi: 10.1021/acs.orglett.1c04316
Chan, Y.-C., Sak, M. H., Frank, S. A. & Miller, S. J. Tunable and cooperative catalysis for enantioselective Pictet-Spengler reaction with varied nitrogen-containing heterocyclic carboxaldehydes. Angew. Chem. Int. Ed. 60, 24573–24581 (2021).
doi: 10.1002/anie.202109694
McInnes, L., Healy, J. & Melville, J. UMAP: uniform manifold approximation and projection for dimension reduction. Preprint at https://arxiv.org/abs/1802.03426 (2018).

Auteurs

Corin C Wagen (CC)

Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA.

Spencer E McMinn (SE)

Discovery Chemistry, Merck & Co. Inc, Boston, MA, USA.

Eugene E Kwan (EE)

Process Research and Development, Merck & Co. Inc, Boston, MA, USA. eugene.kwan@merck.com.

Eric N Jacobsen (EN)

Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA. jacobsen@chemistry.harvard.edu.

Articles similaires

Humans Pharmaceutical Preparations Drug Utilization Prescription Drugs
Risk Assessment Plant Leaves Isomerism Humans Stereoisomerism

Mutational analysis of Phanerochaete chrysosporium´s purine transporter.

Mariana Barraco-Vega, Manuel Sanguinetti, Gabriela da Rosa et al.
1.00
Phanerochaete Fungal Proteins Purines Aspergillus nidulans DNA Mutational Analysis
Osteosarcoma Animals Glutathione Oxidation-Reduction Mice

Classifications MeSH