Indole synthesis - something old, something new

被引:574
作者
Inman, Martyn [1 ]
Moody, Christopher J. [1 ]
机构
[1] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
基金
英国工程与自然科学研究理事会;
关键词
H INSERTION REACTIONS; C BOND FORMATION; N-ARYL ENAMINES; OXIDATIVE CYCLIZATION; INTRAMOLECULAR CYCLIZATION; FISCHER INDOLIZATION; EXPEDIENT SYNTHESIS; RHODIUM CARBENOIDS; ARYLBORONIC ACIDS; TERMINAL ALKYNES;
D O I
10.1039/c2sc21185h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Indoles, both naturally occurring and synthetic, exhibit wide-ranging biological activity. Unusual and complex molecular architectures occur among their natural derivatives. As a result, this important ring system continues to attract attention from the international chemical community, and new methodologies for the construction of this ever relevant heteroaromatic ring continue to be developed. Unfortunately, many methods frequently start from ortho-substituted anilines, thereby greatly restricting the availability of starting materials. A more general approach would start from a mono-functionalized arene such as an aniline or halobenzene, followed by cyclization with C-C or C-N bond formation to an unactivated C-H bond. Such methods are the subject of this perspective.
引用
收藏
页码:29 / 41
页数:13
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