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Recherches sur la formation et la transformation des esters LXIV. Acides aminoalcoylsulfuriques et isothiocyanates: N‐thiocarbamylation sans ou avec alcoylation cyclisante intramoléculaire
Author(s) -
Cherbuliez Emile,
Baehler Br.,
Jaccard S.,
Jindra H.,
Weber G.,
Wyss G.,
Rabinowitz J.
Publication year - 1966
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.19660490124
Subject(s) - chemistry , yield (engineering) , medicinal chemistry , sulfuric acid , alkyl , stereochemistry , organic chemistry , metallurgy , materials science
Aminoalkyl sulfuric monoesters with primary or secondary amino groups – with the exception of colaminesulfuric monoester – react with isothiocyanates in the presence of one equivalent of a base to yield the corresponding hydrosoluble salts of [N‐aryl(aralkyl or alkyl)thiocarbamoyl]‐aminoalkyl sulfates.