Tomaino Elisabetta, Capecchi Eliana, Ubertini Valentina, Piccinino Davide, Bizzarri Bruno M, Saladino Raffaele
Department of Biological and Ecological Sciences, University of Tuscia, Via San Camillo De Lellis s.n.c., Viterbo 01100, Italy.
J Org Chem. 2024 Feb 16;89(4):2343-2350. doi: 10.1021/acs.joc.3c02314. Epub 2024 Jan 29.
This work describes the possibility to combine multicomponent chemistry and multienzymes cascade transformations in a unique reactive framework to yield highly functionalized 1,4-benzoxazines under favorable heterogeneous conditions. The synthetic scheme involved the generation in situ of electrophilic reactive quinone intermediates of tyrosol esters catalyzed by lipase M and tyrosinase followed by nucleophilic 1,6-Michael addition of selected α-amino acid methyl esters, and successive intramolecular lactonization and aromatization processes. The immobilization of the multienzymes cascade on electroactive lignin nanoparticles improved the sustainability and recyclability of the overall system.
这项工作描述了在一个独特的反应框架中结合多组分化学和多酶级联转化的可能性,以便在有利的非均相条件下生成高度官能化的1,4 - 苯并恶嗪。合成方案包括由脂肪酶M和酪氨酸酶催化原位生成亲电反应性酪醇酯醌中间体,随后选定的α - 氨基酸甲酯进行亲核1,6 - 迈克尔加成,以及连续的分子内内酯化和芳构化过程。将多酶级联固定在电活性木质素纳米颗粒上提高了整个系统的可持续性和可回收性。