| Weight | 330.133 g/mol |
|---|---|
| Formula | C19H15BF4 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 3 |
Triphenylcarbenium tetrafluoroborate (341-02-6)
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- A practical triphenylcarbenium tetrafluoroborate mediated one-pot synthesis of 1-substituted N-alkyl-1,2,3,4-tetrahydroisoquinolines (Synthesis, 1992)
- Structures of the tetrafluoroborate salts of triphenylcarbenium ions with one and with two 4-methoxy substituents : stable carbocations (Acta Crystallographica Section C-crystal Structure Communications, 1991)
- Diastereoselective Synthesis of Fluorine-Containing Pyrrolizidines via Triphenylcarbenium Tetrafluoroborate-Promoted Carbofluorination of N-3-Arylpropargylpyrrolidine-Tethered Tertiary Allylic Alcohols (Journal of Organic Chemistry, 2015)
- Organopromoted Direct Synthesis of 1,1-Diphenyl-3-arylindanes via Formal [3+2] Cycloadditions of Triphenylcarbenium Tetrafluoroborate with Styrenes (Synlett, 2016)
- ChemInform Abstract: Reaction of 1,2-Diferrocenylcyclopropanes with Triphenylcarbenium Tetrafluoroborate. (ChemInform, 1988)
- Reaction of Mes NPC1 with Triphenylcarbenium Tetrafluoroborate (Phosphorus Sulfur and Silicon and The Related Elements, 1994)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILES[B-](F)(F)(F)F.C1=CC=C(C=C1)[C+](C2=CC=CC=C2)C3=CC=CC=C3
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InChIKeyVQXBOEYKSVVPSP-UHFFFAOYSA-N
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Triphenylcarbenium tetrafluoroborate
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