Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach

Betke T, Rommelmann P, Oike K, Asano Y, Gröger H (2017)
Angewandte Chemie (International ed. in English) 46(40): 12361-12366.

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Zeitschriftenaufsatz | Veröffentlicht | Englisch
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Zeitschriftentitel
Angewandte Chemie (International ed. in English)
Band
46
Ausgabe
40
Seite(n)
12361-12366
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Betke T, Rommelmann P, Oike K, Asano Y, Gröger H. Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach. Angewandte Chemie (International ed. in English). 2017;46(40):12361-12366.
Betke, T., Rommelmann, P., Oike, K., Asano, Y., & Gröger, H. (2017). Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach. Angewandte Chemie (International ed. in English), 46(40), 12361-12366. doi:10.1002/anie.201702952
Betke, T., Rommelmann, P., Oike, K., Asano, Y., and Gröger, H. (2017). Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach. Angewandte Chemie (International ed. in English) 46, 12361-12366.
Betke, T., et al., 2017. Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach. Angewandte Chemie (International ed. in English), 46(40), p 12361-12366.
T. Betke, et al., “Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach”, Angewandte Chemie (International ed. in English), vol. 46, 2017, pp. 12361-12366.
Betke, T., Rommelmann, P., Oike, K., Asano, Y., Gröger, H.: Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach. Angewandte Chemie (International ed. in English). 46, 12361-12366 (2017).
Betke, Tobias, Rommelmann, Philipp, Oike, Keiko, Asano, Yasuhisa, and Gröger, Harald. “Cyanide-Free and Broadly Applicable Enantioselective Synthetic Platform for Chiral Nitriles through a Biocatalytic Approach”. Angewandte Chemie (International ed. in English) 46.40 (2017): 12361-12366.

6 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Synthesis of Functionalized Nitriles by Microwave-Promoted Fragmentations of Cyclic Iminyl Radicals.
Jackman MM, Im S, Bohman SR, Lo CCL, Garrity AL, Castle SL., Chemistry 24(3), 2018
PMID: 29207207
Biocatalytic Synthesis of Nitriles through Dehydration of Aldoximes: The Substrate Scope of Aldoxime Dehydratases.
Betke T, Higuchi J, Rommelmann P, Oike K, Nomura T, Kato Y, Asano Y, Gröger H., Chembiochem 19(8), 2018
PMID: 29333684
Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles.
Betke T, Maier M, Gruber-Wölfler H, Gröger H., Nat Commun 9(1), 2018
PMID: 30504854
Hot off the press.
Hill RA, Sutherland A., Nat Prod Rep 34(12), 2017
PMID: 29090285

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