Microwave assisted fluorofunctionalization of phenyl substituted alkenes using selectfluor
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- Type
- article
- Published
- 2013-06-01
- Cited by
- 15
- References
- 39
- OpenAlex
- https://openalex.org/W2075070907
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:97959369
Keywords
Selectfluor, Chemistry, Yield (engineering), Electrophile, Double bond
References
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- Ruthenium-catalysed asymmetric transfer hydrogenation of para-substituted α-fluoroacetophenones
- The combination of hydrogen fluoride with organic bases as fluorination agents
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- Transformations of Organic Molecules with F-TEDA-BF4 in Ionic Liquid Media
- Asymmetric reduction using (R)-MeCBS and determination of absolute configuration of para-substituted 2-fluoroarylethanols
- One pot synthesis of side chain fluorinated heterocyclic compounds by microwave irradiation
- Stereochemistry and Some Kinetic Aspects of Fluorination of Phenyl-Substituted Alkenes with SelectfluorTM Reagent F-TEDA-BF4.
- Chelation or Non‐Chelation Control in Addition Reactions of Chiral α‐ and β‐ Alkoxy Carbonyl Compounds [New Synthetic Methods (44)]
- Asymmetric synthesis of chiral organofluorine compounds: use of nonracemic fluoroiodoacetic acid as a practical electrophile and its application to the synthesis of monofluoro hydroxyethylene dipeptide isosteres within a novel series of HIV protease inhibitors.
- Origins of the enantioselectivity observed in oxazaborolidine-catalyzed reductions of ketones
- 1-Fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) as a new, effective reagent for selective fluorofunctionalisation of alkenes under mild reaction conditions
- Novel SO3H-functionalized ionic liquids catalyzed a simple, green and efficient procedure for Fischer indole synthesis in water under microwave irradiation
- Modern synthetic methods for fluorine-substituted target molecules.
- Microwave fluorination: a novel, rapid approach to fluorination with Selectfluor®
Cited by
- Silver-Catalyzed Anti-Markovnikov Hydroxyfluorination of Styrenes
- Recent advances in the synthesis of functionalised monofluorinated compounds.
- Catalyst-free fluorinative alkoxylation of alkenes
- Fluoro-Hydroxylation of gem -Difluoroalkenes: Synthesis of 18 O-labeled α-CF3 Alcohols
- Fluorofunctionalization of C═C Bonds with Selectfluor: Synthesis of β-Fluoropiperazines through a Substrate-Guided Reactivity Switch.
- Catalyst-free regioselective hydroxyfluorination and aminofluorination of α,β-unsaturated ketones.
- Microwave Assisted Fluorofunctionalization of Phenyl Substituted Alkenes Using Selectfluor.
- Evaluation of In-Batch and In-Flow Synthetic Strategies towards the Stereoselective Synthesis of a Fluorinated Analogue of Retro-Thiorphan
- Selectfluor Mediated Difunctionalization of Olefins towards the Synthesis of Fluoromethylated Morpholines
- Branching out: redox strategies towards the synthesis of acyclic α-tertiary ethers.
- Fluorination of alkylidenecyclopropanes and alkylidenecyclobutanes: divergent synthesis of fluorinated cyclopropanes and cyclobutanes.
- Selectfluor and alcohol-mediated synthesis of bicyclic oxyfluorination compounds by Wagner–Meerwein rearrangement
- Recent advances in late-stage monofluorination of natural products and their derivatives
- Bismuth‐Mediated α‐Arylation of Acidic Diketones with ortho‐Substituted Boronic Acids
- Fluorination of Alkenes and Alkynes for Preparing Alkyl Fluorides
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