Atropisomenic amides: Achiral ligands with chiral conformations

被引:26
|
作者
Honda, A [1 ]
Waltz, KM [1 ]
Carroll, PJ [1 ]
Walsh, PJ [1 ]
机构
[1] Univ Penn, Dept Chem, P Roy & Diane T Vagelos Labs, Philadelphia, PA 19104 USA
关键词
atropisomeric amides; titanium; stereochemistry; alkoxide; X-ray structure;
D O I
10.1002/chir.10259
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A new class of achiral ligands With atropisomeric conformations has been coordinated to titanium(IV). The ligands are ortho-hydroxy benzamide derivatives which are deprotonated on reaction with titanium tetraisopropoxide to furnish Ti(L)(2)(O-iPr)(2) complexes (L=ortho-phenoxy benzamide). In these octahedral titanium compounds, the ortho-phenoxy benzamide ligands chelate to titanium, bonding through the phenoxide oxygen and the amide carbonyl oxygen. The benzamide ligands adopt atropisomeric conformations with an angle between the aryl and amide groups of approximately 35degrees. The ligand precursor, ligand, and titanium complexes have been characterized by X-ray crystallography. Only one diastereomer of each titanium complex was observed in the solid state structures. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:615 / 621
页数:7
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