A heavily functionalized atropisomeric biphenyl derivative (4), which is designed to possess a large lateral dipole moment, has been synthesized with use of a Suzuki coupling as the key step and resolved by chiral HPLC. The final coupling reaction is complicated by rapid hydrolytic deboronation of the sterically hindered, electron poor boronate 22. Rigorously anhydrous conditions are therefore necessary to achieve the coupling
A small library of meta- and para-biphenylamines substituted by various alkyl, alkoxy, phenoxy, or h...
2,2′,5,5′-Tetraphenyl-3,3′-bithiophene-4,4′-diol, the first member of a new class of chiral C2-symme...
Background: Atropisomers are very interesting stereoisomers having axial chirality resulting from re...
The biaryl motif is found in many natural and synthetic products that display a wide range of biolog...
Biphenylsarean important class of organic compounds. Theyare importantin the field of natural produc...
R factor = 0.036; wR factor = 0.104; data-to-parameter ratio = 14.5. The title compound, C15H13NO2, ...
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported Li...
Au cours de ce travail, une nouvelle voie de couplage de Suzuki atropo-diastéréosélectif a été mise ...
Amyloid-beta peptide (Abeta) self-assembles into neurotoxic, beta-structured aggregates, which are t...
The synthesis of a new CF3-containing stereogenic atropisomeric pair of ortho-disubstituted biphenyl...
The synthesis of atropisomeric 1,1'-binaphthalenes can be achieved using an asymmetric Suzuki cross-...
The biaryl motif occupies an iconic role in chemistry, being a key structural feature of natural pro...
We report the preparation of axially stereoenriched biphenyls by the coupling of in situ generated a...
Metal-catalyzed cross-coupling reactions are extensively employed in both academia and industry for ...
The preparation of atropisomeric 2,1-borazaronaphthalenes is described. Resolution of the atropisome...
A small library of meta- and para-biphenylamines substituted by various alkyl, alkoxy, phenoxy, or h...
2,2′,5,5′-Tetraphenyl-3,3′-bithiophene-4,4′-diol, the first member of a new class of chiral C2-symme...
Background: Atropisomers are very interesting stereoisomers having axial chirality resulting from re...
The biaryl motif is found in many natural and synthetic products that display a wide range of biolog...
Biphenylsarean important class of organic compounds. Theyare importantin the field of natural produc...
R factor = 0.036; wR factor = 0.104; data-to-parameter ratio = 14.5. The title compound, C15H13NO2, ...
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported Li...
Au cours de ce travail, une nouvelle voie de couplage de Suzuki atropo-diastéréosélectif a été mise ...
Amyloid-beta peptide (Abeta) self-assembles into neurotoxic, beta-structured aggregates, which are t...
The synthesis of a new CF3-containing stereogenic atropisomeric pair of ortho-disubstituted biphenyl...
The synthesis of atropisomeric 1,1'-binaphthalenes can be achieved using an asymmetric Suzuki cross-...
The biaryl motif occupies an iconic role in chemistry, being a key structural feature of natural pro...
We report the preparation of axially stereoenriched biphenyls by the coupling of in situ generated a...
Metal-catalyzed cross-coupling reactions are extensively employed in both academia and industry for ...
The preparation of atropisomeric 2,1-borazaronaphthalenes is described. Resolution of the atropisome...
A small library of meta- and para-biphenylamines substituted by various alkyl, alkoxy, phenoxy, or h...
2,2′,5,5′-Tetraphenyl-3,3′-bithiophene-4,4′-diol, the first member of a new class of chiral C2-symme...
Background: Atropisomers are very interesting stereoisomers having axial chirality resulting from re...