A CONVENIENT PROCEDURE FOR THEREDUCTION OF AMINOACIDS AND AMIDES USING TETRABUTYLAMMONIUM FLUORIDE AND POLYMETHYLHYDROSILOXANE

被引:0
|
作者
Drid, Mohammed Elahbib [1 ,2 ]
Sekhri, Lakhdar [1 ]
Rahim, Oum Elkheir [2 ]
Syed, Abdelkader Hadj [1 ]
Tabchouche, Ahmed [1 ]
机构
[1] Univ Kasdi Merbah, Fac Appl Sci, Proc Engn Dept, Lab Dynam Interact & React Syst, Ouargla 30000, Algeria
[2] Univ Kasdi Merbah, Fac Math & Matter Sci, Chem Dept, Electrochem Lab, Ouargla 30000, Algeria
来源
HETEROCYCLIC LETTERS | 2019年 / 9卷 / 03期
关键词
Reduction; PMHS; TBAF; alpha-aminoacids; amides; CARBOXYLIC-ACIDS; REDUCTION; ESTERS;
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A range of alpha-aminoacids(1a-1h)have been converted efficiently to the corresponding beta-aminoalcohols: 2-amino-3-methylpentan-1-ol (isoleucinol) (2a), 2-amino-4-(methylthio)butan-1-ol (methioninol) (2b), 2-amino-3-methylbutan-1-ol (valinol) (2c), 2-amino-3-(4'-hydroxyphenyl) propan-1-ol (tyrosinol) (2d), 2-amino-3-phenylethan-1-ol (phenylglycinol) (2e), 2-amino-3-phenylpropan-1-ol (phenylalaninol) (2f), 2-aminoethan-1-ol (glycinol) (2g), and 2-aminopropanol-1-ol (alaninol) (2h), with polymethylhydrosiloxane, PMHS, in the presence of catalytic tetrabutylammonium fluoride, TBAF with > 61% yield. Carboxylic acids and their derivatives such as amides(3a and 3b) have also been reducedto the corresponding amines: N-ethylaniline(4a) and N-methylaniline(4b) with polymethylhydrosiloxane, PMHS, in the presence of catalytic tetrabutylammonium fluoride, TBAF with > 74% yield.
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页码:309 / 319
页数:11
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