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Structure elucidation of a condensation product of 4‐aminopyrrole derivatives and dicyclohexylcarbodiimide
Author(s) -
Bialer Meir,
Yagen Boris,
Mechoulam Raphael
Publication year - 1980
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570170834
Subject(s) - chemistry , pyrrole , condensation , organic chemistry , product (mathematics) , stereochemistry , physics , geometry , mathematics , thermodynamics
The chemical structure of the two condensation products of dicyclohexylcarbodiimide (DCC) with the precursors of the mono‐pyrrole homologues of distamycin and with the mono and tri‐pyrrole homologues of congocidine were established. The two products isolated were proven to be condensation products between 4‐aminopyrrole derivatives and dicyclohexylcarbodiimide (DCC).