A chemo-enzymatic oxidation/aldol sequential process directly converts arylbenzyl alcohols and cyclohexanol into chiral β-hydroxy carbonyls. Issue 19 (17th September 2021)

• Record Type: Journal Article
• Authors: Wang, Yu; Wang, Chengyi; Cheng, Qipeng; Su, Yu; Li, Hongyu; Xiao, Rui; Tan, Chunxia; Liu, Guohua
• Is Part Of: Green chemistry. Volume 23:Issue 19(2021)
• Page Start: 7773
• Page End: 7779
• Publication Date: 2021-09-17
• Subjects: Environmental chemistry -- Industrial applications -- Periodicals; Environmental management -- Periodicals; 660
• DOI: 10.1039/d1gc02831f
• Languages: English
• ISSNs: 1463-9262

Abstract

Abstract : An integrated laccase and prolines as a co-catalyst system enables an efficient oxidation/Aldol process to direct access chiral β-hydroxy carbonyls by using alcohols instead of environmentally unfriendly aldehydes and ketones. Abstract : The development of a combination enzyme and organocatalyst for aqueous sequential organic transformation has great significance, in that it is not only environmentally friendly but also overcomes only a single methodological drawback, either in the chemical or biological process. Herein, through the utilization of the bulky steric hindrance of chiral proline derivatives, an integrated laccase and proline as a chemo-enzymatic co-catalyst system is developed. It enables an efficient oxidation/aldol enantioselective sequential reaction to be accomplished, overcoming the mutual deactivation issue. As we present in this study, this one-pot organic transformation, an initial laccase-mediated oxidation of arylbenzyl alcohols and cyclohexanol to form aldehydes and cyclohexanone, followed by a subsequent proline derivative-catalyzed aldol condensation of the in situ generated intermediates, provides various 1, 2-diastereoisomeric chiral β-hydroxy ketones with acceptable yields and high enantio -/diastereoselectivities.