Stereoselectively fluorinated N-heterocycles: a brief survey

被引:75
作者
Hu, Xiang-Guo [1 ]
Hunter, Luke [1 ]
机构
[1] Univ New S Wales, Sch Chem, Sydney, NSW 2052, Australia
来源
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY | 2013年 / 9卷
基金
澳大利亚研究理事会;
关键词
conformation; fluorine; N-heterocycles; iminosugars; medicinal chemistry; organo-fluorine; VAR INCURVATA IFO-9228; ASYMMETRIC-SYNTHESIS; SUBSTITUTED; 3-FLUOROPIPERIDINES; ORGANOFLUORINE CHEMISTRY; SYNTHETIC MODIFICATIONS; GLYCOSIDASE INHIBITORS; NATURAL OCCURRENCE; ACYL-COA; DEOXYFLUORINATION; REGIOSELECTIVITY;
D O I
10.3762/bjoc.9.306
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The stereoselective incorporation of fluorine atoms into N-heterocycles can lead to dramatic changes in the molecules' physical and chemical properties. These changes can be rationally exploited for the benefit of diverse fields such as medicinal chemistry and organocatalysis. This brief review will examine some of the effects that fluorine substitution can have in N-heterocycles, including changes to the molecules' stability, their conformational behaviour, their hydrogen bonding ability, and their basicity. Finally, some methods for the synthesis of stereoselectively fluorinated N-heterocycles will also be reviewed.
引用
收藏
页码:2696 / 2708
页数:13
相关论文
共 80 条
[1]  
Al-Maharik N, 2011, ALDRICHIM ACTA, V44, P65
[2]   Two isosteric fluorinated derivatives of the powerful glucosidase inhibitors, 1-deoxynojirimycin and 2,5-dideoxy-2,5-imino-D-mannitol: Syntheses and glycosidase-inhibitory activities of 1,2,5-trideoxy-2-fluoro-1,5-imino-D-glucitol and of 1,2,5-trideoxy-1-fluoro-2,5-imino-D-mannitol [J].
Andersen, SM ;
Ebner, M ;
Ekhart, CW ;
Gradnig, G ;
Legler, G ;
Lundt, I ;
Stutz, AE ;
Withers, SG ;
Wrodnigg, T .
CARBOHYDRATE RESEARCH, 1997, 301 (3-4) :155-166
[3]  
[Anonymous], 2007, IMINOSUGARS SYNTHESI
[4]   Sugar-mimic glycosidase inhibitors: natural occurrence, biological activity and prospects for therapeutic application [J].
Asano, N ;
Nash, RJ ;
Molyneux, RJ ;
Fleet, GWJ .
TETRAHEDRON-ASYMMETRY, 2000, 11 (08) :1645-1680
[5]   The profound effect of fluorine substitution on the reactivity and regioselectivity of nucleophilic substitution reactions of strained heterocycles. A study of aziridine and its derivatives [J].
Banks, Harold D. .
JOURNAL OF ORGANIC CHEMISTRY, 2006, 71 (21) :8089-8097
[6]   REGIO-SELECTIVITY AND STEREO-SELECTIVITY IN RADICAL REACTIONS [J].
BECKWITH, ALJ .
TETRAHEDRON, 1981, 37 (18) :3073-3100
[7]   The polar hydrophobicity of fluorinated compounds [J].
Biffinger, JC ;
Kim, HW ;
DiMagno, SG .
CHEMBIOCHEM, 2004, 5 (05) :622-627
[8]  
BIRCH AJ, 1969, J CHEM SOC CHEM COMM, P644
[9]   Fluorine in medicinal chemistry: β-fluorination of peripheral pyrrolidines attached to acridine ligands affects their interactions with G-quadruplex DNA [J].
Campbell, Nancy H. ;
Smith, Daniel L. ;
Reszka, Anthony P. ;
Neidle, Stephen ;
O'Hagan, David .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2011, 9 (05) :1328-1331
[10]   Ring expansion induced by DAST:: Synthesis of substituted 3-fluoropiperidines from prolinols and 3-fluoroazepanes from 2-hydroxymethylpiperidines [J].
Dechamps, Ingrid ;
Pardo, Domingo Gomez ;
Cossy, Janine .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2007, 2007 (25) :4224-4234