Synthesis of huge macrocycles using two calix[4]arenes as templates

被引:32
作者
Cao, YD [1 ]
Wang, LY
Bolte, M
Vysotsky, MO
Böhmer, V
机构
[1] Johannes Gutenberg Univ Mainz, Abt Lehramt Chem, Fachbereich Chem Pharm & Geowissensch, D-55099 Mainz, Germany
[2] Goethe Univ Frankfurt, Fachbereich Chem & Pharm Wissensch, Inst Organ Chem, D-60439 Frankfurt, Germany
关键词
D O I
10.1039/b505223h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Macrocycles with up to 100 atoms have been synthesised using two calix[4]arenes as templates: first, (3,5-dialkenyloxy)phenyl groups are attached to the wide rim of a calix[4]arene via urea links, then the alkenyl groups are connected via a metathesis reaction using a tetratosylurea calix[4]arene for their correct prearrangement and finally the urea functions are cleaved to detach the newly formed macrocycles.
引用
收藏
页码:3132 / 3134
页数:3
相关论文
共 22 条
[1]   THE ROLES OF TEMPLATES IN THE SYNTHESES OF PORPHYRIN OLIGOMERS [J].
ANDERSON, S ;
ANDERSON, HL ;
SANDERS, JKM .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1995, (18) :2255-2267
[2]   Nanoscale borromean rings [J].
Cantrill, SJ ;
Chichak, KS ;
Peters, AJ ;
Stoddart, JF .
ACCOUNTS OF CHEMICAL RESEARCH, 2005, 38 (01) :1-9
[3]   Chiral capsules: Asymmetric binding in calixarene-based dimers [J].
Castellano, RK ;
Kim, BH ;
Rebek, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (51) :12671-12672
[4]   Macrocycle synthesis by olefin metathesis on a nanosized, shape-persistent tricationic platinum template [J].
Chuchuryukin, AV ;
Dijkstra, HP ;
Suijkerbuijk, BMJM ;
Gebbink, RJMK ;
van Klink, GPM ;
Mills, AM ;
Spek, AL ;
van Koten, G .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (02) :228-+
[5]  
Diederich F., 2000, TEMPLATED ORGANIC SY
[6]   Resorcinarenes as templates [J].
Gibb, BC .
CHEMISTRY-A EUROPEAN JOURNAL, 2003, 9 (21) :5180-5187
[7]  
Hof F, 2002, ANGEW CHEM INT EDIT, V41, P1488, DOI 10.1002/1521-3773(20020503)41:9<1488::AID-ANIE1488>3.0.CO
[8]  
2-G
[9]  
Höger S, 1999, CHEM-EUR J, V5, P1686, DOI 10.1002/(SICI)1521-3765(19990604)5:6<1686::AID-CHEM1686>3.0.CO
[10]  
2-0