Journal of Molecular Structure, Journal Year: 2024, Volume and Issue: unknown, P. 141010 - 141010
Published: Dec. 1, 2024
Language: Английский
Journal of Molecular Structure, Journal Year: 2024, Volume and Issue: unknown, P. 141010 - 141010
Published: Dec. 1, 2024
Language: Английский
Advanced Science, Journal Year: 2024, Volume and Issue: 11(31)
Published: June 17, 2024
Abstract Oxazocines are key structural intermediates in the synthesis of natural products and pharmaceutical molecules. However, oxazocines especially a highly enantioselective manner, is long‐standing formidable challenge due to unfavorable energetics involved cyclization. Herein, series new PNP‐Ligand P ‐chiral stereocenter first designed synthesized, called MQ‐Phos , successfully applied it Pd‐catalyzed higher‐order formal [4+4]‐cycloaddition α β ‐unsaturated imines with 2‐(hydroxymethyl)‐1‐arylallyl carbonates. The reaction features mild conditions, excellent regio‐ enantiocontrol broad substrate scope (54 examples). Various medium‐sized rings can be afforded moderate yields (up 92%) enantioselectivity 99% ee). newly developed critical for ring catalytic reactivity enantioselectivity.
Language: Английский
Citations
6Advances in heterocyclic chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
Language: Английский
Citations
0RSC Advances, Journal Year: 2025, Volume and Issue: 15(8), P. 6050 - 6067
Published: Jan. 1, 2025
Several fused/binary pyrazole quinolinone hybrids are synthesized via tandem reactions and their insecticidal efficacy against S. littoralis A. gossypii evaluated.
Language: Английский
Citations
0Topics in Current Chemistry, Journal Year: 2023, Volume and Issue: 381(6)
Published: Nov. 3, 2023
Language: Английский
Citations
9Chemistry - A European Journal, Journal Year: 2023, Volume and Issue: 29(70)
Published: Sept. 23, 2023
Abstract Silaspiranes bearing a spiro‐silicon center are promising ring frameworks for the synthesis of novel spirocyclic molecules possessing unique properties. Development efficient methods towards these structures has therefore attracted considerable attentions synthetic chemists. This minireview highlights representative advances in field, and is categorized into four parts according to formation strategies: cyclization, annulation, expansion cycloaddition.
Language: Английский
Citations
7Chemical Communications, Journal Year: 2024, Volume and Issue: 60(29), P. 3958 - 3961
Published: Jan. 1, 2024
A controllable spirocyclization of unsaturated barbiturates with enamines to selectively synthesize spirobarbiturates has been developed under ball-milling conditions.
Language: Английский
Citations
2Chemical Communications, Journal Year: 2024, Volume and Issue: 60(34), P. 4537 - 4540
Published: Jan. 1, 2024
A novel method was devised for regioselective ring expansion of spirocyclopropanes to spirocyclobutanes with stabilized sulfonium ylides, affording 1,2- trans -disubstituted 6,8-dioxaspiro[3.5]nonane-5,9-diones without the formation any isomers.
Language: Английский
Citations
2The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Dec. 18, 2024
In this study, the readily available and inexpensive Sc(OTf)
Language: Английский
Citations
2Advanced Synthesis & Catalysis, Journal Year: 2024, Volume and Issue: 366(11), P. 2596 - 2601
Published: April 9, 2024
Abstract Under the catalysis of Rh 2 (OAc) 4 (10 mol%) and (±)‐Me‐Pybox (20 in 1,2‐DCE at 80 °C, homocoupling/[4+1] cycloaddition cascade diazobarbiturates with diazopyrazolones proceeded readily provided spirobarbiturates 32–88% chemical yields. The structure obtained was identified by X‐ray diffraction analysis.
Language: Английский
Citations
1Russian Chemical Bulletin, Journal Year: 2023, Volume and Issue: 72(10), P. 2453 - 2465
Published: Oct. 1, 2023
Language: Английский
Citations
3