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生物质化学催化转化制备手性化学品:进展与展望

From Biomass to Chiral Chemicals via Chemocatalysis: Advances and Prospects

  • 摘要: 光学纯手性化学品在食品、制药及可降解生物材料等领域具有重要应用价值。木质纤维素生物质主要由(半)纤维素和木质素组成,其丰富的立体结构和多样化功能基团使其成为替代化石资源制备手性化学品的潜在原料。化学催化法高效可控,为手性化学品的制备提供了有利途径。本文综述了经化学催化法由生物质制备包括内酯、羧酸、多元醇、呋喃及寡糖等典型手性化学品的进展。其策略主要分为两类:一是首先由生物质制备非手性平台化学品,随后引入不对称催化剂构建手性中心;二是通过串联反应选择性保留生物质中的天然手性中心,利用其作为“手性池”直接合成目标产物。本文详细讨论了原料体系、合成方法、立体选择性调控及应用研究现状。尽管已取得重要进展,但由生物质定向转化制备光学纯化学品的研究仍处于发展初期。未来研究可集中于:(1)发展生物质手性单元继承与不对称催化的协同新策略;(2)建立精准构筑多手性中心的方法;(3)突破木质素解构与重构技术,发展木质素基手性化合物。这些关键问题的解决有望为可持续手性分子的制备开辟新途径。

     

    Abstract: Optically pure chiral chemicals are important building blocks with widespread applications across multiple scientific and industrial domains such as in pharmaceuticals, agrochemicals, and food, especially acting as precursors to synthesize biodegradable polymers. As an alternative to fossil resources, renewable lignocellulosic biomass has been used to access chiral chemicals, due to the versatile inherent stereostructures and multiple functional groups, such as hydroxyl, carbonyl, and phenyl ether groups. Typically, as the two main units of (hemi)cellulose components in lignocellulosic biomass, D-xylose and D-glucose bear multiple chiral centers (e.g., 2R-3S-4R for D-xylose and 2R-3S-4R-5R for D-glucose). Lignin bears β-O-4 linkages, exhibiting (R,S/S,R) or (R,R/S,S) stereocenters at the side-chain α and β carbon atoms. The valorization of biomass into optically pure chiral chemicals is vital for developing a more sustainable future. This review discusses the production of typical chiral chemicals derived from biomass through chemocatalysis, including lactones (e.g., R/S-valerolactone), carboxylic acids (e.g., D/L-glyceric acid, D/L-lactic acid), polyols (e.g., tetrose), furans, oligosaccharides, and others. Two strategies are generally employed. One approach involves first producing achiral platform chemicals from biomass, followed by the introduction of asymmetric catalysts to reconstruct stereocenters. The second relates to selectively preserving one or more inherent stereocenters in the natural biomass structure during complex cascade reactions in which biomass feedstock acts as a “chiral pool", thus eliminating the establishment of stereocenter. The feedstock, methods employed, and enantioselectivity and applications of the target chiral chemicals are discussed. Despite these advances, the synthesis of optically pure chemicals from biomass is still in its infancy. The coming decade presents both extraordinary challenges and opportunities in biomass-derived chiral chemistry. Future research should be focused on: (1) integrating well-established asymmetric catalysis techniques and methods with biomass’ inherent chiral pools, presenting an unprecedented opportunity to expand the chemical space of sustainable chiral compounds; (2) mastering polyfunctional complexity of chiral chemicals through holistic utilization of biomass’ multichiral centers; (3) unlocking lignin’s stereochemical treasury that represents the next frontier in biomass valorization.

     

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