A new route to vinyl fluorides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. α-Fluoromethyl-n-methyl-phenylsulphoximine: a new fluoromethylenation reagent
2. Stereospecific synthesis of alkenyl fluorides (with retention) via organometallic intermediates
3. Surprising stereochemical control of Wittig olefination involving reaction of fluorine-containing phosphoranium salt and aldehydes
4. CONVENIENT PROCEDURES FOR CONVERSION OF CARBONYL COMPOUNDS TOgem-DIFLUOROOLEFINS AND THEIR SELECTIVE REDUCTIONS TO MONOFLUOROOLEFINS
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1. Fluoroheterocycle formation using fluoroalkynes and their synthetic equivalents;Advances in Heterocyclic Chemistry;2023
2. Synthesis and Reactivity of Electron-Deficient 3-Vinylchromones;SynOpen;2021-08-17
3. Highly E-Selective Synthesis of α-Fluoro-β-arylalkenyl Sulfones from gem-Difluoroalkenes with Sodium Sulfinates;The Journal of Organic Chemistry;2021-04-14
4. SbCl3 initiated conjunctive C–H bond functionalization and carbochlorination between glycine esters and methylenecyclopropanes (MCPs);Chemical Communications;2021
5. Highly stereoselective monofluoroolefination: Facile access to (E)-α-fluorinated arylvinyl sulfones from trifluoromethyl α-fluorinated arylsulfonyl gem-diols;Tetrahedron Letters;2020-06
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