[HTML][HTML] π-Electronic ion pairs: building blocks for supramolecular nanoarchitectonics via i π–i π interactions
Y Haketa, K Yamasumi, H Maeda - Chemical Society Reviews, 2023 - pubs.rsc.org
The pairing of charged π-electronic systems and their ordered arrangement have been
achieved by iπ–iπ interactions that are derived from synergetically worked electrostatic and …
achieved by iπ–iπ interactions that are derived from synergetically worked electrostatic and …
Bis-and trisindolylmethanes (BIMs and TIMs)
The indole ring system is present in many natural products, pharmaceuticals,
agrochemicals, and other compounds of importance. 1–8 The indole unit forms the basis for …
agrochemicals, and other compounds of importance. 1–8 The indole unit forms the basis for …
Copper‐Catalyzed Enantioselective 1,6‐Boration of para‐Quinone Methides and Efficient Transformation of gem‐Diarylmethine Boronates to Triarylmethanes
Y Lou, P Cao, T Jia, Y Zhang, M Wang… - Angewandte …, 2015 - Wiley Online Library
Presented is the first enantioselective copper‐catalyzed 1, 6‐conjugate addition of bis
(pinacolato) diboron to para‐quinone methides. The reaction proceeds with excellent yields …
(pinacolato) diboron to para‐quinone methides. The reaction proceeds with excellent yields …
Cu/chiral phosphoric acid-catalyzed asymmetric three-component radical-initiated 1, 2-dicarbofunctionalization of alkenes
JS Lin, TT Li, JR Liu, GY Jiao, QS Gu… - Journal of the …, 2018 - ACS Publications
An asymmetric intermolecular, three-component radical-initiated dicarbofunctionalization of
1, 1-diarylalkenes with diverse carbon-centered radical precursors and electron-rich …
1, 1-diarylalkenes with diverse carbon-centered radical precursors and electron-rich …
Catalytic Asymmetric 1,6‐Conjugate Addition of para‐Quinone Methides: Formation of All‐Carbon Quaternary Stereocenters
Described herein is a general and mild catalytic asymmetric 1, 6‐conjugate addition of para‐
quinone methides (p‐QMs), a class of challenging reactions with previous limited success …
quinone methides (p‐QMs), a class of challenging reactions with previous limited success …
Organocatalytic asymmetric synthesis of 1, 1-diarylethanes by transfer hydrogenation
A new organocatalytic transfer hydrogenation strategy for the asymmetric synthesis of 1, 1-
diarylethanes is described. Under mild conditions, a range of 1, 1-diarylethanes substituted …
diarylethanes is described. Under mild conditions, a range of 1, 1-diarylethanes substituted …
Synthetic methodologies of achiral diarylmethanols, diaryl and triarylmethanes (TRAMs) and medicinal properties of diaryl and triarylmethanes-an overview
The last decade has witnessed a high demand of various synthetic approaches towards
bioactive achiral diarylmethanols, diaryl and triarylmethanes and the molecules derived …
bioactive achiral diarylmethanols, diaryl and triarylmethanes and the molecules derived …
[HTML][HTML] Light-induced metal-free transformations of unactivated pyridotriazoles
A highly efficient and practical method for incorporation of the arylmethylpyridyl moiety into
diverse molecules has been developed. This method features the transition metal-free light …
diverse molecules has been developed. This method features the transition metal-free light …
Hydrogen bonding network-enabled Brønsted acid-catalyzed Friedel–Crafts reactions: a green approach to access unsymmetrical diaryl-and triarylmethanes
Unsymmetrical di-and triarylmethanes are generally synthesized through metal-catalyzed
cross-coupling or Friedel–Crafts arylation using multistep harsh reaction conditions with pre …
cross-coupling or Friedel–Crafts arylation using multistep harsh reaction conditions with pre …
Recent advances in the synthesis of triarylmethanes by transition metal catalysis
M Nambo, CM Crudden - ACS Catalysis, 2015 - ACS Publications
Triarylmethanes and related compounds are fascinating molecules because of their
structural and physical properties, many potential applications in organic functional …
structural and physical properties, many potential applications in organic functional …