Investigation on the configurative behaviour of pseudolucine in the Walden inversion and on the secession of halogen through diluted alkali from stereoisomeric alpha-bromine-beta-trimethyl-propionyl-amino acids.

被引：27

作者：

Abderhalden, E

Faust, W

Haase, E

机构：

来源：

HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE | 1934年 / 228卷

关键词：

D O I：

10.1515/bchm2.1934.228.3-6.187

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：187 / 197

页数：11

共 7 条

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[2] On the configurative relations of alpha-bromic acids attainable from the optical isomers of isoleucine and alloisoleucine to the amino acids emerging from the amination of the same. An article on the problem of the Walden inversion
Abderhalden, E
Zeisset, W
[J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1931, 200 : 179 - 190
[3] Tests on the configurative behaviour of isoleucine in Walden's reversal.
Abderhalden, E
Schweitzer, F
[J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1932, 206 : 116 - 124
[4] Division of synthetically prepared isoleucine in its four optic-active components, namely 1-(+) and d-(-) isoleucine, along with d-(-) and l-(+) alloisoleucine
Abderhalden, E
Zeisset, W
[J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1931, 195 : 121 - 131
[5] 1914, H-S Z PHYSIOL CHEM, V89, P517
[6] 1923, PFLUGERS ARCH, V201, P3
[7] 1889, MH CHEM, V10, P771