The behaviour of thiazole-5-carboxylic acid-ester-iodine-methylate in reduction experiments

被引：8

作者：

Erlenmeyer, H

Epprecht, A

von Meyenburg, H

机构：

来源：

HELVETICA CHIMICA ACTA | 1937年 / 20卷

关键词：

D O I：

10.1002/hlca.19370200177

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：514 / 515

页数：2

共 11 条

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Erlenmeyer, H ;

von Meyenburg, H .

HELVETICA CHIMICA ACTA, 1937, 20 :204-206

[2] Experimental models concerning the hydrogen transfer action groups of cofermentation [J].

Karrer, P ;

Ringier, BH ;

Buchi, J ;

Fritzsche, H ;

Solmssen, U .

HELVETICA CHIMICA ACTA, 1937, 20 :55-71

[3] Reduction products of nicotinic acid-amide-iodine methylate [J].

Karrer, P ;

Schwarzenbach, G ;

Benz, F ;

Solmssen, U .

HELVETICA CHIMICA ACTA, 1936, 19 :811-828

[4]

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[5] Dihydro-pyridine compounds IV. N-phenyl-o-dihydro-pyridine and N-p-methoxyphenyl-o-dihydro-pyridine [J].

Karrer, P ;

Schwarzenbach, G ;

Utzinger, GE .

HELVETICA CHIMICA ACTA, 1937, 20 :72-79

[6]

KARRER P, 1936, LEHRBUCH ORG CHEM, V4, P783

[7]

KARRER P, 1937, HELV CHIM ACTA, V20, P66

[8]

Karrer P., 1936, HELV CHIM ACTA, V19, P1028

[9] Hydrogenation of vitamin B1 [J].

Lipmann, F .

NATURE, 1936, 138 :1097-1098

[10]

MEYER V, LEHRBUCH ORG CHEM, V3, P536

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