Micalizio Glenn C, Hale Sarah B
Department of Chemistry, Burke Laboratory, Dartmouth College, Hanover, New Hampshire 03755, United States.
Acc Chem Res. 2015 Mar 17;48(3):663-73. doi: 10.1021/ar500408e. Epub 2015 Feb 10.
Convergent C-C bond-forming reactions define the fabric of organic synthesis and, when applied in complex molecule synthesis, can have a profound impact on efficiency by decreasing the longest linear sequence of transformations required to convert simple starting materials to complex targets. Despite their well-appreciated strategic significance, campaigns in natural product synthesis typically embrace only a small suite of reactivity to achieve such bond construction (i.e., nucleophilic addition to polarized π-bonds, nucleophilic substitution, cycloaddition, and metal-catalyzed "cross-coupling"), therefore limiting the sites at which convergent coupling chemistry can be strategically employed. In our opinion, it is far too often that triumphs in the field are defined by chemical sequences that do not address the challenges associated with discovery, development, and production of natural product-inspired agents. We speculated that advancing an area of chemical reactivity not represented in the few well-established strategies for convergent C-C bond formation may lead to powerful new retrosynthetic relationships that could simplify approaches to the syntheses of a variety of different classes of natural products. Our studies ultimately embraced the pursuit of strategies to control the course of metallacycle-mediated "cross-coupling" between substrates containing sites of simple π-unsaturation (ubiquitous functionality in organic chemistry including alkenes, alkynes, allenes, aldehydes, and imines, among others). In just eight years since our initial publication in this area, we have defined over 20 stereoselective intermolecular C-C bond-forming reactions that provide access to structural motifs of relevance for the synthesis of polyketides, fatty acids, alkaloids, and terpenes, while doing so in a direct and stereoselective fashion. These achievements continue to serve as the foundation of my group's activity in natural product and function-oriented synthesis, where our achievements in reaction development are challenged in the context of complex targets. Among our early efforts, we achieved the most concise synthesis of a benzoquinone ansamycin ever described (macbecin I), and moved beyond this achievement to explore the role of our chemistry in function-oriented synthesis targeting the discovery of natural product-inspired Hsp90 inhibitors. These later efforts have led to the discovery of a uniquely selective benzoquinone ansamycin-inspired Hsp90 inhibitor that lacks the problematic quinone present in the natural series. This achievement was made possible by a concise chemical synthesis pathway that had at its core the application of metallacycle-mediated cross-coupling chemistry.
收敛性碳-碳键形成反应决定了有机合成的架构,当应用于复杂分子合成时,通过减少将简单起始原料转化为复杂目标所需的最长线性转化序列,可对效率产生深远影响。尽管它们具有公认的战略意义,但天然产物合成中的研究通常仅采用一小部分反应活性来实现此类键的构建(即对极化π键的亲核加成、亲核取代、环加成以及金属催化的“交叉偶联”),因此限制了可战略性应用收敛偶联化学的位点。在我们看来,该领域的成功往往由那些未解决与天然产物启发的药物发现、开发和生产相关挑战的化学序列所定义。我们推测,推进一个在已确立的少数收敛性碳-碳键形成策略中未体现的化学反应领域,可能会产生强大的新逆合成关系,从而简化各种不同类天然产物合成的方法。我们的研究最终致力于探索控制含简单π-不饱和位点的底物(包括烯烃、炔烃、联烯、醛和亚胺等有机化学中普遍存在的官能团)之间金属环介导的“交叉偶联”过程的策略。自我们在该领域首次发表论文以来的短短八年时间里,我们已经定义了20多种立体选择性分子间碳-碳键形成反应,这些反应能够直接且立体选择性地提供与聚酮化合物、脂肪酸、生物碱和萜类化合物合成相关的结构基序。这些成就继续作为我们团队在天然产物和功能导向合成活动的基础,在复杂目标的背景下,我们在反应开发方面的成就面临着挑战。在我们早期的努力中,我们实现了有史以来最简洁的苯醌安莎霉素(马贝菌素I)合成,并在此基础上进一步探索我们的化学在以发现天然产物启发的Hsp90抑制剂为目标的功能导向合成中的作用。这些后期的努力导致发现了一种独特的选择性苯醌安莎霉素启发的Hsp90抑制剂,它没有天然系列中存在的有问题的醌。这一成就得益于一条简洁的化学合成途径,其核心是金属环介导的交叉偶联化学的应用。