METHODS AND POSSIBILITIES OF NUCLEOPHILIC ACYLATION

被引:333
作者
SEEBACH, D
机构
[1] Institut für Organische Chemie, Universität Karlsruhe, Richard-Willstätter-Allee
关键词
Acylation; Nucleophilic reactions;
D O I
10.1002/anie.196906391
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nucleophilic acylation is the attachment of an (Formula Presented.) group to an electrophilic center. A brief discussion of the advantages offered by acylations of this type in syntheses is followed by a description of the direct methods (reactions with acylmetal compounds) and the methods proceeding via “masked” acyl anions. The latter methods are based on the use of either metalated vinyl ether derivatives or carbanions derived from acetals. Organyllithiums of sulfur‐stabilized carbanions are important reagents of this type. Copyright © 1969 by Verlag Chemie, GmbH, Germany
引用
收藏
页码:639 / &
相关论文
共 167 条
[1]  
[Anonymous], 1967, ANGEW CHEM, V79, P15
[2]  
ARENS JF, 1959, RECL TRAV CHIM PAY B, V78, P663
[3]  
ARENS JF, 1968, RECUEIL TRAV CHIM PA, V87, P97
[4]  
ARENS JF, 1963, RECUEIL TRAV CHIM PA, V82, P1040
[5]  
ARENS JF, 1961, RECUEIL TRAV CHIM PA, V80, P244
[6]  
ARENS JF, 1966, RECUEIL TRAV CHIM PA, V85, P580
[7]  
BANK KC, 1969, CHEM COMMUN, P8
[8]   PREPARATION OF [FORMYL-2H]- AND [FORMYL-3H]-ALDEHYDES [J].
BENNETT, DJ ;
KIRBY, GW ;
MOSS, VA .
CHEMICAL COMMUNICATIONS, 1967, (05) :218-&
[9]  
BENT HA, 1966, ORGANIC SULFUR COMPO, V2, P1
[10]   CONDENSATION OF 2-ARYL-1,3-DIOXOLANES WITH ALKYLLITHIUM REAGENTS . A NEW SYNTHESIS OF ALKYL ARYL KETONES FROM AROMATIC ALDEHYDES [J].
BERLIN, KD ;
RATHORE, BS ;
PETERSON, M .
JOURNAL OF ORGANIC CHEMISTRY, 1965, 30 (01) :226-&