DICARBOXYLIC-ACID BIS(METHYL PHOSPHATES) - ANIONIC BIOMIMETIC CROSS-LINKING REAGENTS

被引:42
作者
KLUGER, R
GRANT, AS
BEARNE, SL
TRACHSEL, MR
机构
[1] Lash Miller Chemical Laboratories, Department of Chemistry, University of Toronto, Toronto, Ontario
关键词
D O I
10.1021/jo00296a056
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Monoesters of acyl phosphates are anionic electrophiles and their difunctional analogues are expected to function as site-directed cross-linking reagents. Dimethyl phosphate anhydrides of mono- and dicarboxylic acids are conveniently prepared by the reaction of an acyl chloride with sodium dimethyl phosphate in tetrahydrofuran. These are converted to monomethyl acyl phosphates by reaction with sodium iodide. Methyl acetyl phosphate and a representative group of symmetrical difunctional bis(methyl phosphates) (1a-5a) were prepared by this route. Hemoglobin is cross-linked in its reactions with difunctional methyl acyl phosphates. © 1990, American Chemical Society. All rights reserved.
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页码:2864 / 2868
页数:5
相关论文
共 29 条
[21]   REACTIONS OF TOLUIC ACIDS WITH SULFUR .1. STILBENEDICARBOXYLIC ACIDS [J].
TOLAND, WG ;
WILKES, JB ;
BRUTSCHY, FJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (09) :2263-2264
[22]  
UENO H, 1989, J BIOL CHEM, V264, P12344
[23]   SITE-SPECIFIC MODIFICATION OF HEMOGLOBIN BY METHYL ACETYL PHOSPHATE [J].
UENO, H ;
POSPISCHIL, MA ;
MANNING, JM ;
KLUGER, R .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1986, 244 (02) :795-800
[24]  
WALSH C, 1979, ENZYMATIC REACTION M, P234
[25]  
WALSH C, 1979, ENZYMATIC REACTION M, P241
[26]  
WEBER K, 1969, J BIOL CHEM, V244, P4406
[27]  
WHETSTONE R, 1953, Patent No. 2648896
[28]   A METHOD FOR THE PREPARATION OF UNESTERIFIED ACYL PHOSPHATES VIA STANNYL PHOSPHATE INTERMEDIATES [J].
YAMAGUCHI, K ;
KAMIMURA, T ;
HATA, T .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (13) :4534-4536
[29]   DEALKYLATION AND DEBENZYLATION OF TRIESTERS OF PHOSPHORIC ACID - PHOSPHORYLATION OF HYDROXY AND AMINO COMPOUNDS [J].
ZERVAS, L ;
DILARIS, I .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (20) :5354-5357