Thiol additions to acrylates by fluorous mixture synthesis: relative control of elution order in demixing by the fluorous tag and the thiol substituent

被引:45
作者
Curran, DP [1 ]
Oderaotoshi, Y [1 ]
机构
[1] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
基金
美国国家卫生研究院;
关键词
mixture synthesis; fluorous synthesis; solution phase combinatorial chemistry;
D O I
10.1016/S0040-4020(01)00369-6
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
All possible combinations of a series of three fluorous benzyl tags and three acrylates have been made. The resulting acrylate esters were combined in groups of three (one of each tag) and the resulting mixtures were reacted with a mixture of four thiols under standard conditions to effect conjugate addition. Analysis of the resulting libraries by fluorous hplc showed a primary separation based on the tag and revealed reliable secondary separations based on the thiol and the acrylate. The primary and secondary separations were used together in a preparative 'mixture of mixtures' experiment in which one of the tagged acrylate mixtures was reacted with a mixture of three thiols. The resulting nine component mixture was demixed by fluorous and reverse phase hplc and then detagged to give all nine final products in pure form. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:5243 / 5253
页数:11
相关论文
共 15 条
[1]  
[Anonymous], COMBINATORIAL CHEM P
[2]  
BERENDSEN GE, 1980, ANAL CHEM, V52, P1990, DOI 10.1021/ac50062a056
[3]   GEOMETRICAL MODEL FOR CHEMICALLY BONDED TMS AND PDS PHASES [J].
BERENDSEN, GE ;
GALAN, LD .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1978, 1 (04) :403-426
[4]   RETENTION AND SELECTIVITY CHARACTERISTICS OF A NONPOLAR PERFLUORINATED STATIONARY PHASE FOR LIQUID-CHROMATOGRAPHY [J].
BILLIET, HAH ;
SCHOENMAKERS, PJ ;
DEGALAN, L .
JOURNAL OF CHROMATOGRAPHY, 1981, 218 (1-3) :443-454
[5]   Multistep convergent solution-phase combinatorial synthesis and deletion synthesis deconvolution [J].
Boger, DL ;
Chai, WY ;
Jin, Q .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (29) :7220-7225
[6]   NEW PROMISE IN COMBINATORIAL CHEMISTRY - SYNTHESIS, CHARACTERIZATION, AND SCREENING OF SMALL-MOLECULE LIBRARIES IN SOLUTION [J].
CARELL, T ;
WINTNER, EA ;
SUTHERLAND, AJ ;
REBEK, J ;
DUNAYEVSKIY, YM ;
VOUROS, P .
CHEMISTRY & BIOLOGY, 1995, 2 (03) :171-183
[7]   Thermal allylations of aldehydes with a fluorous allylstannane. Separation of organic and fluorous products by solid phase extraction with fluorous reverse phase silica gel [J].
Curran, DP ;
Hadida, S ;
He, M .
JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (20) :6714-6715
[8]  
CURRAN DP, UNPUB SYNLETT
[9]   Mixture-based synthetic combinatorial libraries [J].
Houghten, RA ;
Pinilla, C ;
Appel, JR ;
Blondelle, SE ;
Dooley, CT ;
Eichler, J ;
Nefzi, A ;
Ostresh, JM .
JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (19) :3743-3778
[10]  
Kainz S, 1998, SYNTHESIS-STUTTGART, P1425