Página principal > Artículos > Asymmetric organocatalyzed phospha-michael addition for the direct synthesis of biologically active chromenylphosphonates
Resumen: The potential of phosphites as nucleophiles for the asymmetric synthesis of chiral chromene derivatives has been overlooked in the literature. Herein, we report a promising approach via asymmetric organocatalyzed phospha‐Michael addition to iminochromenes, using a bifunctional squaramide, which gives access to chromenylphosphonates, an interesting family of bioactive compounds. Our optimized protocol provides very good reactivity, affording yields of up to 95% and with chiral products exhibiting an enantiomeric excess of up to 98%. Idioma: Inglés DOI: 10.1002/adsc.202300563 Año: 2023 Publicado en: Advanced Synthesis and Catalysis 365, 19 (2023), 3234-3240 ISSN: 1615-4150 Factor impacto JCR: 4.4 (2023) Categ. JCR: CHEMISTRY, ORGANIC rank: 8 / 58 = 0.138 (2023) - Q1 - T1 Categ. JCR: CHEMISTRY, APPLIED rank: 19 / 74 = 0.257 (2023) - Q2 - T1 Factor impacto CITESCORE: 9.4 - Organic Chemistry (Q1) - Catalysis (Q2)