Highly selective and high-yielding rotaxane synthesis via aminolysis of prerotaxanes consisting of a ring component and a stopper unit

被引:37
作者
Hirose, Keiji [1 ]
Nishihara, Keiji [1 ]
Harada, Naoki [1 ]
Nakamura, Yamato [1 ]
Masuda, Daisuke [1 ]
Araki, Masami [1 ]
Tobe, Yoshito [1 ]
机构
[1] Osaka Univ, Div Frontier Mat Sci, Grad Sch Engn Sci, Toyonaka, Osaka 5638531, Japan
关键词
D O I
10.1021/ol070999w
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A highly rotaxane-selective synthesis via aminolysis of prerotaxanes, which were composed of a phenolic pseudo-crown ether as a ring component and a bulky stopper unit, was developed. The best result was obtained in the case of aminolysis of 3b with 3,5-dimethylbenzylamine which proceeded quantitatively with ca. 100% rotaxane selectivity forming the corresponding rotaxane 5b. The rotaxanes were formed by kinetically controlled attack of the amine from the backside of the ring component of the prerotaxanes.
引用
收藏
页码:2969 / 2972
页数:4
相关论文
共 14 条
[1]   The slipping approach to self-assembling [n]rotaxanes [J].
Asakawa, M ;
Ashton, PR ;
Ballardini, R ;
Balzani, V ;
Belohradsky, M ;
Gandolfi, MT ;
Kocian, O ;
Prodi, L ;
Raymo, FM ;
Stoddart, JF ;
Venturi, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (02) :302-310
[2]   Self-assembly, spectroscopic, and electrochemical properties of [n]rotaxanes [J].
Ashton, PR ;
Ballardini, R ;
Balzani, V ;
Belohradsky, M ;
Gandolfi, MT ;
Philp, D ;
Prodi, L ;
Raymo, FM ;
Reddington, MV ;
Spencer, N ;
Stoddart, JF ;
Venturi, M ;
Williams, DJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (21) :4931-4951
[3]  
ASHTON PR, 1993, CHEM COMMUN, P1269
[4]   A new reaction pathway in the ester aminolysis catalyzed by glymes and crown ethers [J].
Basilio, Nuno ;
Garcia-Rio, Luis ;
Mejuto, Juan C. ;
Perez-Lorenzo, Moises .
JOURNAL OF ORGANIC CHEMISTRY, 2006, 71 (11) :4280-4285
[5]   Non-rusty [2]catenanes with huge rings and their polymers [J].
Godt, A .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2004, 2004 (08) :1639-1654
[6]   Synthesis of [1]rotaxane via covalent bond formation and its unique fluorescent response by energy transfer in the presence of lithium ion [J].
Hiratani, K ;
Kaneyama, M ;
Nagawa, Y ;
Koyama, E ;
Kanesato, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (42) :13568-13569
[7]   A new synthetic method for rotaxanes via tandem Claisen rearrangement, diesterification, and aminolysis [J].
Hiratani, K ;
Suga, J ;
Nagawa, Y ;
Houjou, H ;
Tokuhisa, H ;
Numata, M ;
Watanabe, K .
TETRAHEDRON LETTERS, 2002, 43 (33) :5747-5750
[8]   Preparation of phenolic chiral crown ethers and podands and their enantiomer recognition ability toward secondary amines [J].
Hirose, K ;
Fujiwara, A ;
Matsunaga, K ;
Aoki, N ;
Tobe, Y .
TETRAHEDRON-ASYMMETRY, 2003, 14 (05) :555-566
[9]   Chiral recognition of secondary amines by using chiral crown ether and podand [J].
Hirose, K ;
Fujiwara, A ;
Matsunaga, K ;
Aoki, N ;
Tobe, Y .
TETRAHEDRON LETTERS, 2002, 43 (47) :8539-8542
[10]   FINGERPRINTING A TRANSITION-STRUCTURE GUEST BY A BUILDING-BLOCK APPROACH WITH AN INCREMENTAL SERIES OF CATALYTIC HOSTS - STRUCTURAL REQUIREMENTS FOR GLYME AND ALPHA,OMEGA-DIMETHOXYALKANE CATALYZES IN N-METHYLBUTYLAMINOLYSIS AND BUTYLAMINOLYSIS OF 4-NITROPHENYL ACETATE IN CHLOROBENZENE [J].
HOGAN, JC ;
GANDOUR, RD .
JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (01) :55-61