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4,5‐Dihalogen‐O‐acetylindoxyle
Author(s) -
Kambli Ed.
Publication year - 1964
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19640470809
Subject(s) - chemistry , esterase , stereochemistry , combinatorial chemistry , selection (genetic algorithm) , enzyme , biochemistry , artificial intelligence , computer science
In the synthesis of 4‐chloro‐5‐bromo‐O‐acetyl indoxyl, an important substance used in locating esterase activity, difficulties arose from the formation of isomeric intermediate products. Selection of different starting compounds not only facilitates the syntheses of this dihalogeno O‐acetyl indoxyl, but also enables the production of new o‐acetyl indoxyls of equal applicability.