Structure-stability correlations for imine formation in aqueous solution

被引:241
作者
Godoy-Alcántar, C
Yatsimirsky, AK
Lehn, JM
机构
[1] Univ Louis Pasteur Strasbourg 1, Inst Sci & Ingn Supramol, F-67083 Strasbourg, France
[2] Univ Autonoma Estado Morelos, Ctr Invest Quim, Cuernavaca 62210, Morelos, Mexico
[3] Univ Nacl Autonoma Mexico, Fac Quim, Mexico City 04510, DF, Mexico
关键词
amine; aldehyde; imine formation; structure-stability correlations;
D O I
10.1002/poc.941
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Imine formation between 25 aldehydes and 13 amines in aqueous solution in the pH range 7-11 was studied by H-1 NMR spectroscopy. A three-parameter linear equation correlating logarithms of imine formation constants with pK(a) and HOMO energies of amines and LUMO energies of aldehydes is proposed. In view of the widespread occurrence of imine-forming processes in both chemistry and biology, the data presented are of significance for physical organic chemistry and of particular interest for dynamic combinatorial chemistry. Copyright (c) 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:979 / 985
页数:7
相关论文
共 60 条
[41]  
Patai S., 1970, CHEM CARBON NITROGEN, P64
[42]  
Patai S., 1966, CHEM CARBONYL GROUP, P600
[43]  
Patai S., 1968, CHEM AMINO GROUP, P350
[44]  
Polyakov VA, 1999, J PHYS ORG CHEM, V12, P357, DOI 10.1002/(SICI)1099-1395(199905)12:5<357::AID-POC129>3.0.CO
[45]  
2-Y
[46]   Drug discovery by dynamic combinatorial libraries [J].
Ramström, O ;
Lehn, JM .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (01) :26-36
[47]   Dynamic combinatorial carbohydrate libraries:: Probing the binding site of the concanavalin A lectin [J].
Ramström, O ;
Lohmann, S ;
Bunyapaiboonsri, T ;
Lehn, JM .
CHEMISTRY-A EUROPEAN JOURNAL, 2004, 10 (07) :1711-1715
[48]   Simultaneous selection, amplification and isolation of a pseudo-peptide receptor by an immobilised N-methyl ammonium ion template [J].
Roberts, SL ;
Furlan, RLE ;
Cousins, GRL ;
Sanders, JKM .
CHEMICAL COMMUNICATIONS, 2002, (09) :938-939
[49]  
Rowan SJ, 2002, ANGEW CHEM INT EDIT, V41, P898, DOI 10.1002/1521-3773(20020315)41:6<898::AID-ANIE898>3.0.CO
[50]  
2-E