Synthesis of Chiral Thiourea-Thioxanthone Hybrids
Ontology highlight
ABSTRACT: Four different 1-aminocyclohexanes bearing a tethered thioxanthone group in the 2-position were prepared. The synthesis commenced with the respective N-protected β-amino acids, the carboxyl group of which was employed for the introduction of the thioxanthone moiety. After construction of the thioxanthone and protecting group removal, the conversion of the amino group into the respective thiourea was accomplished by treatment with
SUBMITTER: Mayr F
PROVIDER: S-EPMC6376629 | biostudies-literature | 2017 Oct
REPOSITORIES: biostudies-literature
ACCESS DATA
