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 …
Strategic evolution in transition metal-catalyzed directed C–H bond activation and future directions
In the field of C–H bond functionalization chemistry, directed C–H bond activation strategies
are highly appreciated due to the high efficiency and selectivity of such reactions towards a …
are highly appreciated due to the high efficiency and selectivity of such reactions towards a …
Photoinduced copper-catalyzed late-stage azidoarylation of alkenes via arylthianthrenium salts
The arylethylamine pharmacophore is conserved across a range of biologically active
natural products and pharmaceuticals, particularly in molecules that act on the central …
natural products and pharmaceuticals, particularly in molecules that act on the central …
Intermolecular radical carboamination of alkenes
H Jiang, A Studer - Chemical Society Reviews, 2020 - pubs.rsc.org
Vicinal alkene carboamination is a highly efficient and practical synthetic strategy for the
straightforward preparation of diverse and valuable amine derivatives starting from simple …
straightforward preparation of diverse and valuable amine derivatives starting from simple …
Metal-free photochemical imino-alkylation of alkenes with bifunctional oxime esters
The concurrent installation of C–C and C–N bonds across alkene frameworks represents a
powerful tool to prepare motifs that are ubiquitous in pharmaceuticals and bioactive …
powerful tool to prepare motifs that are ubiquitous in pharmaceuticals and bioactive …
Visual kinetic analysis
CDT Nielsen, J Burés - Chemical science, 2019 - pubs.rsc.org
Visual kinetic analyses extract meaningful mechanistic information from experimental data
using the naked-eye comparison of appropriately modified progress reaction profiles. Basic …
using the naked-eye comparison of appropriately modified progress reaction profiles. Basic …
Chiral arylsulfinylamides as reagents for visible light-mediated asymmetric alkene aminoarylations
C Hervieu, MS Kirillova, Y Hu, S Cuesta-Galisteo… - Nature Chemistry, 2024 - nature.com
Two-or one-electron-mediated difunctionalizations of internal alkenes represent
straightforward approaches to assemble molecular complexity by the simultaneous …
straightforward approaches to assemble molecular complexity by the simultaneous …
Arylsulfonylacetamides as bifunctional reagents for alkene aminoarylation
Alkene aminoarylation with a single, bifunctional reagent is a concise synthetic strategy. We
report a catalytic protocol for the addition of arylsulfonylacetamides across electron-rich …
report a catalytic protocol for the addition of arylsulfonylacetamides across electron-rich …
Transition‐Metal‐Catalyzed Three‐Component Difunctionalizations of Alkenes
JS Zhang, L Liu, T Chen, LB Han - Chemistry–An Asian Journal, 2018 - Wiley Online Library
Three‐component reactions can directly convert three reactants into the desired products in
one pot and thus greatly shorten the synthetic path. Recently, transition‐metal catalysis has …
one pot and thus greatly shorten the synthetic path. Recently, transition‐metal catalysis has …
NiH-catalysed proximal-selective hydroalkylation of unactivated alkenes and the ligand effects on regioselectivity
XX Wang, YT Xu, ZL Zhang, X Lu, Y Fu - Nature Communications, 2022 - nature.com
Alkene hydrocarbonation reactions have been developed to supplement traditional
electrophile-nucleophile cross-coupling reactions. The branch-selective hydroalkylation …
electrophile-nucleophile cross-coupling reactions. The branch-selective hydroalkylation …