Li Junqi, Grillo Anthony S, Burke Martin D
Howard Hughes Medical Institute and Roger Adams Laboratory, Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.
Acc Chem Res. 2015 Aug 18;48(8):2297-307. doi: 10.1021/acs.accounts.5b00128. Epub 2015 Jul 22.
The study and optimization of small molecule function is often impeded by the time-intensive and specialist-dependent process that is typically used to make such compounds. In contrast, general and automated platforms have been developed for making peptides, oligonucleotides, and increasingly oligosaccharides, where synthesis is simplified to iterative applications of the same reactions. Inspired by the way natural products are biosynthesized via the iterative assembly of a defined set of building blocks, we developed a platform for small molecule synthesis involving the iterative coupling of haloboronic acids protected as the corresponding N-methyliminodiacetic acid (MIDA) boronates. Here we summarize our efforts thus far to develop this platform into a generalized and automated approach for small molecule synthesis. We and others have employed this approach to access many polyene-based compounds, including the polyene motifs found in >75% of all polyene natural products. This platform further allowed us to derivatize amphotericin B, the powerful and resistance-evasive but also highly toxic last line of defense in treating systemic fungal infections, and thereby understand its mechanism of action. This synthesis-enabled mechanistic understanding has led us to develop less toxic derivatives currently under evaluation as improved antifungal agents. To access more Csp(3)-containing small molecules, we gained a stereocontrolled entry into chiral, non-racemic α-boryl aldehydes through the discovery of a chiral derivative of MIDA. These α-boryl aldehydes are versatile intermediates for the synthesis of many Csp(3) boronate building blocks that are otherwise difficult to access. In addition, we demonstrated the utility of these types of building blocks in accessing pharmaceutically relevant targets via an iterative Csp(3) cross-coupling cycle. We have further expanded the scope of the platform to include stereochemically complex macrocyclic and polycyclic molecules using a linear-to-cyclized strategy, in which Csp(3) boronate building blocks are iteratively assembled into linear precursors that are then cyclized into the cyclic frameworks found in many natural products and natural product-like structures. Enabled by the serendipitous discovery of a catch-and-release protocol for generally purifying MIDA boronate intermediates, the platform has been automated. The synthesis of 14 distinct classes of small molecules, including pharmaceuticals, materials components, and polycyclic natural products, has been achieved using this new synthesis machine. It is anticipated that the scope of small molecules accessible by this platform will continue to expand via further developments in building block synthesis, Csp(3) cross-coupling methodologies, and cyclization strategies. Achieving these goals will enable the more generalized synthesis of small molecules and thereby help shift the rate-limiting step in small molecule science from synthesis to function.
小分子功能的研究与优化常常受到用于制备此类化合物的耗时且依赖专业人员的过程的阻碍。相比之下,已经开发出了用于合成肽、寡核苷酸以及越来越多的寡糖的通用且自动化的平台,在这些平台中,合成被简化为相同反应的迭代应用。受天然产物通过一组特定构建模块的迭代组装进行生物合成方式的启发,我们开发了一个小分子合成平台,该平台涉及作为相应N - 甲基亚氨基二乙酸(MIDA)硼酸酯保护的卤代硼酸的迭代偶联。在此,我们总结了到目前为止我们为将这个平台发展成为一种通用且自动化的小分子合成方法所做的努力。我们和其他人已经采用这种方法获得了许多基于多烯的化合物,包括在所有多烯天然产物中超过75%发现的多烯基序。这个平台还使我们能够对两性霉素B进行衍生化,两性霉素B是治疗系统性真菌感染的强大且不易产生耐药性但毒性也很高的最后一道防线,从而了解其作用机制。这种基于合成的机理理解促使我们开发目前正在评估的毒性较低的衍生物作为改进的抗真菌剂。为了获得更多含Csp(3)的小分子,我们通过发现MIDA的一种手性衍生物,实现了对手性、非外消旋α - 硼基醛的立体控制合成。这些α - 硼基醛是合成许多其他难以获得的Csp(3)硼酸酯构建模块的通用中间体。此外,我们展示了这些类型的构建模块在通过迭代Csp(3)交叉偶联循环获得药学相关靶点方面的效用。我们进一步将该平台的范围扩展到包括使用线性到环化策略的立体化学复杂的大环和多环分子,其中Csp(3)硼酸酯构建模块被迭代组装成线性前体,然后环化形成许多天然产物和类天然产物结构中发现的环状框架。由于偶然发现了一种用于普遍纯化MIDA硼酸酯中间体的捕获 - 释放协议,该平台已实现自动化。使用这台新的合成机器已经实现了14种不同类别的小分子的合成,包括药物、材料成分和多环天然产物。预计通过构建模块合成、Csp(3)交叉偶联方法和环化策略的进一步发展,这个平台可获得的小分子范围将继续扩大。实现这些目标将使小分子的合成更加通用化,从而有助于将小分子科学中的限速步骤从合成转移到功能研究。