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331 |
ChemInform Abstract: Selective and Scalable Synthesis of Trifluoromethanesulfenamides and Fluorinated Unsymmetrical Disulfides Using a Shelf‐Stable Electrophilic SCF 3 Reagent.
Enthalten in ChemInform Bd. 46, 2015, Nr. 21: no-no. 1 S.
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332 |
ChemInform Abstract: Self‐Optimizing Reactor Systems: Algorithms, On‐Line Analytics, Setups, and Strategies for Accelerating Continuous Flow Process Optimization
Enthalten in ChemInform Bd. 45, 2014, Nr. 25: no-no. 1 S.
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333 |
ChemInform Abstract: Shedding Light on Broensted Acid Catalysis — A Photocyclization—Reduction Reaction for the Asymmetric Synthesis of Tetrahydroquinolines from Aminochalcones in Batch and Flow.
Enthalten in ChemInform Bd. 45, 2013, Nr. 2: no-no. 1 S.
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334 |
ChemInform Abstract: Shedding Light on Organocatalysis—Light‐Assisted Asymmetric Ion‐Pair Catalysis for the Enantioselective Hydrogenation of Pyrylium Ions.
Enthalten in ChemInform Bd. 44, 2013, Nr. 50: no-no. 1 S.
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335 |
ChemInform Abstract: Synthesis of Indoles Using Visible Light: Photoredox Catalysis for Palladium‐Catalyzed C—H Activation.
Enthalten in ChemInform Bd. 46, 2015, Nr. 17: no-no. 1 S.
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336 |
ChemInform Abstract: The First General, Efficient and Highly Enantioselective Reduction of Quinoxalines and Quinoxalinones.
Enthalten in ChemInform Bd. 41, 2010, Nr. 26: no-no. 1 S.
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337 |
ChemInform Abstract: Thieme Chemistry Journal Awardees — Where Are They Now? Asymmetric Broensted Acid Catalyzed Transfer Hydrogenations
Enthalten in ChemInform Bd. 41, 2010, Nr. 25: no-no. 1 S.
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338 |
ChemInform Abstract: Tin‐Free Visible Light Photoredox Catalyzed Cyclization of Enamides as a Mild Procedure for the Synthesis of γ‐Lactams.
Enthalten in ChemInform Bd. 47, 2016, Nr. 51: no-no. 1 S.
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339 |
ChemInform Abstract: Trifluoromethylselenolation of Aryldiazonium Salts: A Mild and Convenient Copper‐Catalyzed Procedure for the Introduction of the SeCF 3 Group.
Enthalten in ChemInform Bd. 47, 2016, Nr. 28: no-no. 1 S.
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340 |
ChemInform Abstract: Trifluoromethylthiolation of Unsymmetrical λ 3 ‐Iodane Derivatives: Additive‐Free, Selective and Scalable Introduction of the SCF 3 Group.
Enthalten in ChemInform Bd. 47, 2016, Nr. 27: no-no. 1 S.
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