Site-Selective Molecular Transformation: Acylation of Hydroxy Groups and C-H Amination

被引:2
|
作者
Ueda, Yoshihiro [1 ]
机构
[1] Kyoto Univ, Inst Chem Res, Uji, Kyoto 6110011, Japan
基金
日本学术振兴会;
关键词
site selectivity; catalyst; acylation; C-H amination; glucose; total synthesis; HEPARAN-SULFATE EXPRESSION; AQUILINUM VAR LATIUSCULUM; REGIOSELECTIVE ACYLATION; NATURAL-PRODUCTS; PHENYL(BROMODICHLOROMETHYL)MERCURY-DERIVED DICHLOROCARBENE; NONCOVALENT INTERACTIONS; ORGANOSILICON COMPOUNDS; BOND FUNCTIONALIZATION; HYDROLYZABLE TANNINS; BRACKEN FERN;
D O I
10.1248/cpb.c21-00425
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Control of site selectivity is an exciting direction for synthetic organic chemistry owing to the possibility of selective modification of multifunctionalized molecules, ultimately including biomacromolecules. In this review, our recent research related to site selectivity in two types of transformation, namely, the acylation of hydroxy groups and C-H amination, is summarized. Regarding the acylation of hydroxy groups, catalystcontrolled site selectivity enables unconventional retrosynthetic analysis, leading to efficient syntheses of sugar-related natural and unnatural products. Regarding C-H amination, the discovery of unprecedented reaction sites in intermolecular amination mediated by dirhodium nitrenes is described. The findings of this research demonstrate the power of site-selective transformation in the synthesis of a particular class of compounds.
引用
收藏
页码:931 / 944
页数:14
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