Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8675, Japan.
Molecular Chirality Research Center, Chiba University, 1-33, Yayoi-cho, Inage-ku, Chiba 263-8522, Japan.
J Am Chem Soc. 2021 Jan 20;143(2):604-611. doi: 10.1021/jacs.0c10682. Epub 2020 Dec 31.
Arene dearomatization is a straightforward method for converting an aromatic feedstock into functionalized carbocycles. Enantioselective dearomatizations of chemically inert arenes, however, are quite limited and underexplored relative to those of phenols and indoles. We developed a method for diazo-free generation of silver-carbene species from an ynamide and applied it to the dearomatization of nonactivated arenes. Transiently generated norcaradiene could be trapped by intermolecular [4 + 2] cycloaddition, synthesizing polycycles with five consecutive stereogenic centers. This protocol constitutes the first highly enantioselective reaction based on the diazo-free generation of silver-carbene species. Mechanistic investigations revealed a dearomatization followed by two different classes of pericyclic reactions, as well as the origin of the chemo- and enantioselectivity.
芳烃脱芳构化是将芳构化原料转化为功能化碳环的一种直接方法。然而,相对于酚类和吲哚类化合物,化学惰性芳烃的对映选择性脱芳构化反应相当有限,且研究不足。我们开发了一种从炔酰胺中无重氮生成银卡宾物种的方法,并将其应用于非活化芳烃的脱芳构化反应中。瞬态生成的降蒈二烯可以通过分子间[4+2]环加成进行捕获,合成具有五个连续手性中心的多环化合物。该方案构成了第一个基于银卡宾物种无重氮生成的高对映选择性反应。机理研究表明,该反应经历了脱芳构化,随后是两类不同的周环反应,以及化学和对映选择性的起源。