Brief introduction of Tri-tert-butylphosphonium tetrafluoroborate

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Application In Synthesis of Tri-tert-butylphosphonium tetrafluoroborate, you can also check out more blogs about131274-22-1

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.131274-22-1, Name is Tri-tert-butylphosphonium tetrafluoroborate, molecular formula is C12H28BF4P. In a Patent，once mentioned of 131274-22-1, Application In Synthesis of Tri-tert-butylphosphonium tetrafluoroborate

6-O-Acyl ketolide antibacterials of the formula: 1wherein R1, R2, R3, R4, W, X, X?, Y, and Y? are as described herein and in which the substituents have the meaning indicated in the description. These compounds are useful as antibacterial agents.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Application In Synthesis of Tri-tert-butylphosphonium tetrafluoroborate, you can also check out more blogs about131274-22-1

Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate