Wadsworth Andrew D, Naysmith Briar J, Brimble Margaret A
School of Chemical Sciences, The University of Auckland, 23 Symonds Street, Auckland 1010, New Zealand.
School of Chemical Sciences, The University of Auckland, 23 Symonds Street, Auckland 1010, New Zealand; Maurice Wilkins Centre for Molecular Biodiscovery, c/o The University of Auckland, Private Bag 92019, Auckland, New Zealand.
Eur J Med Chem. 2015 Jun 5;97:816-29. doi: 10.1016/j.ejmech.2014.11.038. Epub 2014 Nov 22.
Since the first reported synthesis of an α-carboline almost a century ago, there has been a steady interest in the development of strategies towards this unique heterocyclic motif. This interest can mainly be attributed to a range of biological activity displayed by the α-carboline natural products including cytotoxicity, anticancer properties or CNS activity. Numerous studies have led to the development of a number of alternative methods to prepare simple α-carbolines as well as a range of synthetic α-carboline derived compounds.
自近一个世纪前首次报道α-咔啉的合成以来,人们一直对开发针对这一独特杂环结构的合成策略保持着持续的兴趣。这种兴趣主要归因于α-咔啉天然产物所表现出的一系列生物活性,包括细胞毒性、抗癌特性或中枢神经系统活性。众多研究促使人们开发出了多种制备简单α-咔啉以及一系列合成α-咔啉衍生化合物的替代方法。