HFIP in organic synthesis
HF Motiwala, AM Armaly, JG Cacioppo… - Chemical …, 2022 - ACS Publications
1, 1, 1, 3, 3, 3-Hexafluoroisopropanol (HFIP) is a polar, strongly hydrogen bond-donating
solvent that has found numerous uses in organic synthesis due to its ability to stabilize ionic …
solvent that has found numerous uses in organic synthesis due to its ability to stabilize ionic …
Technological innovations in photochemistry for organic synthesis: flow chemistry, high-throughput experimentation, scale-up, and photoelectrochemistry
Photoinduced chemical transformations have received in recent years a tremendous amount
of attention, providing a plethora of opportunities to synthetic organic chemists. However …
of attention, providing a plethora of opportunities to synthetic organic chemists. However …
Photoinduced borylation for the synthesis of organoboron compounds: focus review
Organoboron compounds have important synthetic value and can be applied in numerous
transformations. The development of practical and convenient ways to synthesize boronate …
transformations. The development of practical and convenient ways to synthesize boronate …
Reductive electrophotocatalysis: merging electricity and light to achieve extreme reduction potentials
We describe a new electrophotocatalytic strategy that harnesses the power of light and
electricity to generate an excited radical anion with a reducing potential of− 3.2 V vs SCE …
electricity to generate an excited radical anion with a reducing potential of− 3.2 V vs SCE …
Hexafluoroisopropanol as a highly versatile solvent
I Colomer, AER Chamberlain, MB Haughey… - Nature Reviews …, 2017 - nature.com
Abstract 1, 1, 1, 3, 3, 3-Hexafluoroisopropanol (HFIP) has recently become a very popular
solvent or additive with applications across the spectrum of chemistry. Analysis shows that it …
solvent or additive with applications across the spectrum of chemistry. Analysis shows that it …
Transition-Metal-Free, Visible-Light-Enabled Decarboxylative Borylation of Aryl N-Hydroxyphthalimide Esters
L Candish, M Teders, F Glorius - Journal of the American …, 2017 - ACS Publications
Herein, we report a conceptually novel borylation reaction proceeding via a mild
photoinduced decarboxylation of redox-activated aromatic carboxylic acids. This work …
photoinduced decarboxylation of redox-activated aromatic carboxylic acids. This work …
Metal‐Free Radical Borylation of Alkyl and Aryl Iodides
A metal‐free radical borylation of alkyl and aryl iodides with bis (catecholato) diboron
(B2cat2) as the boron source under mild conditions is introduced. The borylation reaction is …
(B2cat2) as the boron source under mild conditions is introduced. The borylation reaction is …
Selective C− N borylation of alkyl amines promoted by Lewis base
J Hu, G Wang, S Li, Z Shi - Angewandte Chemie International …, 2018 - Wiley Online Library
An efficient method for the metal‐free deaminative borylation of alkylamines, using bis
(catecholato) diboron as the boron source, to directly synthesize various alkyl potassium …
(catecholato) diboron as the boron source, to directly synthesize various alkyl potassium …
Decarboxylative borylation of aliphatic esters under visible-light photoredox conditions
D Hu, L Wang, P Li - Organic letters, 2017 - ACS Publications
The conventional methods for preparing alkyl boronates often necessitate anhydrous and
demanding reaction conditions. Herein, a new, operationally simple decarboxylative …
demanding reaction conditions. Herein, a new, operationally simple decarboxylative …
Metal‐Free Stereoconvergent C− H Borylation of Enamides
T Wang, ZJ Wang, M Wang, L Wu… - Angewandte Chemie …, 2023 - Wiley Online Library
Enamides, functional derivatives of enamines, play a significant role as synthetic targets.
However, the stereoselective synthesis of these molecules has posed a longstanding …
However, the stereoselective synthesis of these molecules has posed a longstanding …