Hexafluoroisopropanol (HFIP) as a multifunctional agent in gold-catalyzed cycloisomerizations and sequential transfor-mations

05 April 2023, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Despite the unique position of gold catalysis in contemporary organic synthesis, this area of research is notorious for requiring activators and/or additives that enable catalysis by generating cationic forms of gold catalysts. Cycloisomeriza-tion reactions occupy a significant portion of the gold-catalyzed reaction space, while they represent a diverse family of reactions which are frequently utilized in synthesis. Herein, hexafluoroisopropanol (HFIP) is shown to be a uniquely simple tool for gold-catalyzed cycloisomerizations, rendering the use of external activators obsolete, and leading to high-ly active catalytic systems with ppm levels of catalyst loading in certain cases. HFIP assumes a dual role as solvent and activator, operating via the dynamic activation of the Au-Cl bond through hydrogen bonding, which initiates the catalytic cycle. This special mode of catalysis can enable efficient and scalable cyclization reactions of propargylamides and ynoic acids with simple [AuCl(L)] complexes. A thorough screening of ancillary ligands and counter anions has been per-formed, establishing this methodology as an alternative to elaborate ligand/catalyst design and to the use of activators. Additionally, this concept is applied in C-C bond forming cycloisomerization reactions leading to 2H-chromenes and to the design of catalytic systems for sequential or one-pot transformations leading to activated ketoesters, a functionalized N-heterocyclic carbene (NHC) precursor salt, and a compound bearing the bioactive indole core, among others. Im-portantly, through mechanistic investigations including a “snapshot” of the species of interest in the solid state, we were able to unambiguously detect the key H-bonding interaction between HFIP and the gold catalyst, shedding light on the intermolecular mode of activation that enables catalysis. In the cases examined herein, HFIP is not only an excellent sol-vent, but also a potent activator and a valuable synthetic handle when incorporated into functional groups of products.

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Experimental procedures, additional optimization experi-ments, mechanistic experiments, computational information, compound characterization data and copies of spectra.
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