共 49 条
Interplay between the diamine structure and absolute helicity in Ni-salen metallofoldamers
被引:19
作者:
Dong, Zhenzhen
[1
]
Bai, Shi
[1
]
Yap, Glenn P. A.
[1
]
Fox, Joseph M.
[1
]
机构:
[1] Univ Delaware, Brown Labs, Dept Chem & Biochem, Newark, DE 19803 USA
关键词:
SITE-SELECTIVE TRANSMETALATION;
DIELS-ALDER REACTIONS;
ASYMMETRIC EPOXIDATION;
(SALEN)MANGANESE(III) COMPLEX;
ABIOTIC METALLOFOLDAMERS;
SECONDARY STRUCTURE;
LIGAND;
CATALYST;
METAL;
TRANS-CYCLOHEXANE-1,2-DIAMINE;
D O I:
10.1039/c0cc04794e
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The nature of internal chiral diamines can greatly influence the ratio of helical diastereomers for Ni-salen based metallofoldamers. The diastereomer ratio is small for metallofoldamers derived from (1R, 2R)-cyclohexanediamine, (11R, 12R)-9,10-dihydro-9,10-ethanoanthracene-11,12-diamine, or (1R, 2R)-cyclopentanediamine. By contrast, the foldamer from (1S, 2S)-1,2-diphenylethylenediamine provides a relatively large bias (6 : 1) for the P-helical diastereomer as evidenced by NMR studies, chiroptical data, and X-ray studies. A model is proposed to explain the origin of the helical bias. These findings underscore the need to consider helical diastereomers in models for asymmetric induction in metal-salen catalyzed reactions.
引用
收藏
页码:3781 / 3783
页数:3
相关论文