- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
-
Semi-Industrial Fluorination of β-Keto Esters with SF4: Safety vs Efficacy ; volume:31 ; number:06 ; year:2020 ; pages:565-574
Synlett ; 31, Heft 06 (2020), 565-574
- Contributor
-
Trofymchuk, Serhii A.
Kliukovskyi, Denys V.
Semenov, Sergey V.
Khairulin, Andrii R.
Shevchenko, Valerii O.
Bugera, Maksym Y.
Tarasenko, Karen V.
Volochnyuk, Dmitriy M.
Ryabukhin, Sergey V.
- DOI
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10.1055/s-0037-1610744
- URN
-
urn:nbn:de:101:1-2020052806190006791948
- Rights
-
Open Access unbekannt; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:51 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Trofymchuk, Serhii A.
- Kliukovskyi, Denys V.
- Semenov, Sergey V.
- Khairulin, Andrii R.
- Shevchenko, Valerii O.
- Bugera, Maksym Y.
- Tarasenko, Karen V.
- Volochnyuk, Dmitriy M.
- Ryabukhin, Sergey V.
Other Objects (12)
Enantioselective Alkylation of β-Keto Esters
Organocatalytic Trifluoromethylthiolation of β-Keto Esters
Enantioselective Homologation of α-Keto Esters with α-Diazo Esters
CONVERSION OF α-ARYLIDENE-γ-ΚEΤΟ ESTERS TO DIARYLFURAN CARBOXYLIC ACID ESTERS†
Copper-catalyzed cascade reactions of α,β-unsaturated esters with keto esters
Semi-rational engineering an aldo–keto reductase for stereocomplementary reduction of α-keto amide compounds
β-Phenylalanine Ester Synthesis from Stable β-Keto Ester Substrate Using Engineered ω-Transaminases
Photocatalytic Benzylic Fluorination
Asymmetric Allylic Alkylation of Acyclic β‑Keto Esters Catalyzed by Iridium
Formation of Complex α-Imino Esters via Multihetero-Cope Rearrangement of α-Keto Ester Derived Nitrones
Fluorination of Aryl Trifluoroborates
Fluorination of antimonene hexagons†
Enantioselective Alkylation of β-Keto Esters
Organocatalytic Trifluoromethylthiolation of β-Keto Esters
Enantioselective Homologation of α-Keto Esters with α-Diazo Esters
CONVERSION OF α-ARYLIDENE-γ-ΚEΤΟ ESTERS TO DIARYLFURAN CARBOXYLIC ACID ESTERS†
Copper-catalyzed cascade reactions of α,β-unsaturated esters with keto esters
Semi-rational engineering an aldo–keto reductase for stereocomplementary reduction of α-keto amide compounds
β-Phenylalanine Ester Synthesis from Stable β-Keto Ester Substrate Using Engineered ω-Transaminases
Photocatalytic Benzylic Fluorination
Asymmetric Allylic Alkylation of Acyclic β‑Keto Esters Catalyzed by Iridium
Formation of Complex α-Imino Esters via Multihetero-Cope Rearrangement of α-Keto Ester Derived Nitrones
Fluorination of Aryl Trifluoroborates
Fluorination of antimonene hexagons†
Enantioselective Alkylation of β-Keto Esters
Organocatalytic Trifluoromethylthiolation of β-Keto Esters
Enantioselective Homologation of α-Keto Esters with α-Diazo Esters
CONVERSION OF α-ARYLIDENE-γ-ΚEΤΟ ESTERS TO DIARYLFURAN CARBOXYLIC ACID ESTERS†
Copper-catalyzed cascade reactions of α,β-unsaturated esters with keto esters
Semi-rational engineering an aldo–keto reductase for stereocomplementary reduction of α-keto amide compounds
β-Phenylalanine Ester Synthesis from Stable β-Keto Ester Substrate Using Engineered ω-Transaminases
Photocatalytic Benzylic Fluorination
Asymmetric Allylic Alkylation of Acyclic β‑Keto Esters Catalyzed by Iridium
Formation of Complex α-Imino Esters via Multihetero-Cope Rearrangement of α-Keto Ester Derived Nitrones
Fluorination of Aryl Trifluoroborates