ACS Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 2939 - 2949
Published: Feb. 4, 2025
Language: Английский
ACS Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 2939 - 2949
Published: Feb. 4, 2025
Language: Английский
Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 62(15)
Published: Feb. 7, 2023
This study establishes the first organocatalytic enantioselective synthesis of axially chiral N,N'-bisindoles via phosphoric acid-catalyzed formal (3+2) cycloadditions indole-based enaminones as novel platform molecules with 2,3-diketoesters, where de novo indole-ring formation is involved. Using this new strategy, various were synthesized in good yields and excellent enantioselectivities (up to 87 % yield 96 ee). More importantly, class exhibited some degree cytotoxicity toward cancer cells was derived into phosphine ligands high catalytic activity. provides a strategy for using asymmetric organocatalysis realize applications such scaffolds medicinal chemistry catalysis.
Language: Английский
Citations
91Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 63(3)
Published: Nov. 2, 2023
With the rapid development of asymmetric catalysis, demand for enantioselective synthesis complex and diverse molecules with different chiral elements is increasing. Owing to unique features atropisomerism, catalytic atropisomers has attracted a considerable interest from chemical science community. In particular, introducing additional elements, such as carbon centered chirality, heteroatomic planar helical into provides an opportunity incorporate new properties axially compounds, thus expanding potential applications atropisomers. Thus, it important perform transformations synthesize bearing multiple elements. spite challenges in transformations, recent years, chemists have devised powerful strategies under organocatalysis or metal synthesizing wide range enantioenriched Therefore, become emerging field. This review summarizes progress this field indicates challenges, thereby promoting horizon.
Language: Английский
Citations
83Science China Chemistry, Journal Year: 2023, Volume and Issue: 66(4), P. 966 - 992
Published: Feb. 15, 2023
Language: Английский
Citations
82Journal of the American Chemical Society, Journal Year: 2023, Volume and Issue: 145(12), P. 6944 - 6952
Published: March 15, 2023
Enantioselective metallaphotoredox catalysis, which combines photoredox catalysis and asymmetric transition-metal has become an effective approach to achieve stereoconvergence under mild conditions. Although many impressive synthetic approaches have been developed access central chirality, the construction of axial chirality by still remains underexplored. Herein, we report two visible light-induced cobalt-catalyzed reductive couplings biaryl dialdehydes synthesize axially chiral aldehydes (60 examples, up 98% yield, >19:1 dr, >99% ee). This protocol shows good functional group tolerance, broad substrate scope, excellent diastereo- enantioselectivity.
Language: Английский
Citations
82Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 62(14)
Published: Feb. 10, 2023
Axially chiral diaryl ethers are a type of unique atropisomers bearing two potential axes, which have applications in variety research fields. However, the catalytic enantioselective synthesis these ether is largely underexplored when compared to asymmetric biaryl or other types atropisomers. Herein, we report highly efficient through an organocatalyzed desymmetrization protocol. The phosphoric acid-catalyzed electrophilic aromatic aminations symmetrical 1,3-benzenediamine substrates afforded series excellent yields and enantioselectivities. facile construction heterocycles by utilizations 1,2-benzenediamine moiety products provided access structurally diverse novel azaarene-containing
Language: Английский
Citations
50Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 62(31)
Published: April 25, 2023
Axially chiral compounds have been always considered a laboratory curiosity with rare prospects of being applied in asymmetric synthesis. Things changed very quickly the last twenty years when it was understood important role and enormous impact that these medicinal, biological material chemistry. The synthesis atropisomers became rapidly expanding field recent reports on development N-N strongly prove how this research is hot topic open to new challenges frontiers This review focuses advances enantioselective highlighting strategies breakthroughs obtain novel stimulating atropisomeric framework.
Language: Английский
Citations
49Nature Reviews Chemistry, Journal Year: 2024, Volume and Issue: 8(7), P. 497 - 517
Published: June 18, 2024
Language: Английский
Citations
21ACS Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 2351 - 2358
Published: Jan. 24, 2025
Language: Английский
Citations
3Angewandte Chemie International Edition, Journal Year: 2022, Volume and Issue: 62(3)
Published: Nov. 25, 2022
Abstract A Cu/CPA co‐catalytic system has been developed for achieving the direct hydrophosphinylation of alkynes with phosphine oxides in delivering novel axially chiral phosphorus‐containing alkenes high yields and excellent enantioselectivities (up to 99 % yield ee). DFT calculations were performed elucidate reaction pathway origin enantiocontrol. This streamlined modular methodology establishes a new platform design application styrene‐phosphine ligands.
Language: Английский
Citations
49ACS Catalysis, Journal Year: 2023, Volume and Issue: 13(4), P. 2565 - 2575
Published: Feb. 6, 2023
We present herein an unprecedented stereoselective synthesis of triaryl-2-pyrones with monoaxial or contiguous diaxes from readily available starting materials. This N-heterocyclic carbene catalysis method adopts atroposelective annulation 2-aryketones ynals under oxidative conditions. The includes the construction one two axes in a single operation, achieves step economy, and affords axially chiral moderate to good yields, high excellent enantioselectivities. DFT calculations relative energies stereoisomers rotational barriers were performed.
Language: Английский
Citations
43