A family of novel squaramides/sulfamides based on 1,2-alkamine was developed as chiral bifunctional catalysts to promote the asymmetric alcoholysis of meso cyclic anhydrides. The hemiesters were obtained in high yield...A family of novel squaramides/sulfamides based on 1,2-alkamine was developed as chiral bifunctional catalysts to promote the asymmetric alcoholysis of meso cyclic anhydrides. The hemiesters were obtained in high yield with up to 93% ee. The usefulness of this methodology was demonstrated in the asymmetric synthesis of the key intermediate of P2X7 receptor antagonists.展开更多
Series of coumarins containing heterocyclic substituent in 3-position were prepared. Sulfonyl chloride, a reactive group, was drawn into the heterocycle, and further condensed with amines to give series of new compoun...Series of coumarins containing heterocyclic substituent in 3-position were prepared. Sulfonyl chloride, a reactive group, was drawn into the heterocycle, and further condensed with amines to give series of new compounds that contain N-alkyl sulfamide. The spectral properties and dyeing character of these new dyes are discussed. A bathochromic shift (10 nm), enhanced fastness in light and sublimation (1-2 grade) and larger molar extinction coefficient (increase 104 L ·mol-1 ·cm-1) are apparent with these new compounds. In the meantime, larger solubility appears with these new compounds.展开更多
文摘A family of novel squaramides/sulfamides based on 1,2-alkamine was developed as chiral bifunctional catalysts to promote the asymmetric alcoholysis of meso cyclic anhydrides. The hemiesters were obtained in high yield with up to 93% ee. The usefulness of this methodology was demonstrated in the asymmetric synthesis of the key intermediate of P2X7 receptor antagonists.
文摘Series of coumarins containing heterocyclic substituent in 3-position were prepared. Sulfonyl chloride, a reactive group, was drawn into the heterocycle, and further condensed with amines to give series of new compounds that contain N-alkyl sulfamide. The spectral properties and dyeing character of these new dyes are discussed. A bathochromic shift (10 nm), enhanced fastness in light and sublimation (1-2 grade) and larger molar extinction coefficient (increase 104 L ·mol-1 ·cm-1) are apparent with these new compounds. In the meantime, larger solubility appears with these new compounds.
