Ring-Expansion Reactions in the Synthesis of Macrocycles and Medium-Sized Rings

被引:227
作者
Donald, James R. [1 ]
Unsworth, William P. [1 ]
机构
[1] Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
关键词
macrocycles; medium-sized rings; rearrangements; ring enlargement; ring expansion; DIVERSITY-ORIENTED SYNTHESIS; AZA-CLAISEN REARRANGEMENT; HYDROGEN-BONDING SITES; 1ST TOTAL-SYNTHESIS; BETA-KETO-ESTERS; HOMO-COPE-TYPE; TRANSAMIDATION REACTIONS; ZIP-REACTION; STEREOSELECTIVE-SYNTHESIS; RADICAL FRAGMENTATION;
D O I
10.1002/chem.201700467
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Functionalised macrocycles and medium-sized rings have applications in a number of scientific fields, ranging from medicinal chemistry and supramolecular chemistry, to catalysis and nanotechnology. However, their value in these areas can be undermined by a simple, but important limitation: large ring systems are very often difficult to make. Traditional end-to-end cyclisation reactions of long linear precursors are typically unpredictable and impractical processes, mainly due to unfavourable enthalpic and entrop-ic factors. Most published methods to make large rings focus on minimising the damage inflicted by performing the difficult cyclisation step; in contrast, ring-expansion reactions enable it to be avoided altogether. In this Review article, it is highlighted how "growing" rings from existing cyclic systems via ring expansion can expedite the efficient, practical and scalable synthesis of macrocycles and medium-sized rings.
引用
收藏
页码:8780 / 8799
页数:20
相关论文
共 250 条
[1]   Biological activity of synthetic ionophores: ion transporters as prospective drugs? [J].
Alfonso, Ignacio ;
Quesada, Roberto .
CHEMICAL SCIENCE, 2013, 4 (08) :3009-3019
[2]  
[Anonymous], 2016, Angew. Chem
[3]  
[Anonymous], 1978, ANGEW CHEM, V90, P210
[4]  
[Anonymous], 2004, ANGEW CHEM
[5]  
[Anonymous], 2015, ANGEW CHEM, V127, P16020
[6]   Three-carbon Dowd-Beckwith ring expansion reaction versus intramolecular 1,5-hydrogen transfer reaction: A theoretical study [J].
Ardura, D ;
Sordo, TL .
JOURNAL OF ORGANIC CHEMISTRY, 2005, 70 (23) :9417-9423
[7]   Studies towards the total synthesis of taxoids: a rapid entry into bicyclo[6.4.0]dodecane ring system. Part 1 [J].
Arseniyadis, S ;
Ferreira, MDR ;
del Moral, JQ ;
Hernando, JIM ;
Potier, P ;
Toupet, L .
TETRAHEDRON-ASYMMETRY, 1998, 9 (22) :4055-4071
[8]   TICL4-MEDIATED REACTIONS OF ALKYL AZIDES WITH CYCLIC-KETONES [J].
AUBE, J ;
MILLIGAN, GL ;
MOSSMAN, CJ .
JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (06) :1635-1637
[9]   INTRAMOLECULAR SCHMIDT REACTION OF ALKYL AZIDES [J].
AUBE, J ;
MILLIGAN, GL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (23) :8965-8966
[10]   Synthesis of α-heterosubstituted glycine derivatives from dihaloethanamides [J].
Bailey, PD ;
Baker, SR ;
Boa, AN ;
Clayson, J ;
Rosair, GM .
TETRAHEDRON LETTERS, 1998, 39 (42) :7755-7758