ACS Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 16996 - 17003
Published: Nov. 4, 2024
Language: Английский
ACS Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 16996 - 17003
Published: Nov. 4, 2024
Language: Английский
Science China Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Oct. 25, 2024
Language: Английский
Citations
2Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: 11(10), P. 2733 - 2738
Published: Jan. 1, 2024
Herein we present a practical approach for preparing 10 B-enriched 2,1-borazaronaphthalenes from o -aminostyrenes and BF 3 (the primary source of boron-10) in the presence chlorosilane.
Language: Английский
Citations
1Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)
Published: Nov. 30, 2024
The catalytic asymmetric synthesis of axially chiral alkenes remains a daunting challenge due to the lower rotational barrier, especially for longer stereogenic axis (e.g. C-B axis). radical difunctionalization alkynes represents an efficient strategy these targets. Key success such transformations lies in aryl-stabilized highly reactive alkenyl intermediates, however, it elusive whether boryl group could play similar role. Here we report nickel-catalyzed atroposelective relayed reductive coupling reaction our designed ethynyl-azaborines with simple alkyl and aryl halides through boron-stabilized vinyl intermediate. This transformation enables straightforward access challenging alkenylborons bearing generally high enantioselectivity excellent stereoselectivity. axis. authors alkyl/aryl
Language: Английский
Citations
1Angewandte Chemie, Journal Year: 2024, Volume and Issue: 136(10)
Published: Jan. 10, 2024
Abstract Skeletal editing of N ‐heterocycles has recently received considerable attention, and the introduction boron atom into heterocycles often results in positive property changes. However, direct enlargement through insertion is rarely reported literature. Here, we report a ‐heterocyclic reaction combination C−H borylation, accessing fused‐BN‐heterocycles. The synthetic potential this chemistry was demonstrated by substrate scope late‐stage diversification products.
Language: Английский
Citations
0Angewandte Chemie, Journal Year: 2024, Volume and Issue: 136(30)
Published: May 15, 2024
Abstract Atropisomers hold significant fascination, not only for their prevalence in natural compounds but also biological importance and wide‐ranging applications as chiral materials, ligands, organocatalysts. While biaryl heterobiaryl atropisomers are commonly studied, the enantioselective synthesis of less abundant heteroatom‐linked non‐biaryl presents a formidable challenge modern organic synthesis. Unlike classical atropisomers, these molecules allow rotation around two bonds, resulting low barriers to enantiomerization through concerted bond rotations. In recent years discovery new configurationally stable rare scaffolds such aryl amines, ethers sulfones well innovative methodologies control configuration have been disclosed literature constitute topic this minireview.
Language: Английский
Citations
0ACS Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 16996 - 17003
Published: Nov. 4, 2024
Language: Английский
Citations
0