Structure elucidation of a condensation product of 4‐aminopyrrole derivatives and dicyclohexylcarbodiimide

Meir Bialer; Boris Yagen; Raphael Mechoulam

doi:10.1002/jhet.5570170834

Structure elucidation of a condensation product of 4‐aminopyrrole derivatives and dicyclohexylcarbodiimide

Meir Bialer^*
, Boris Yagen
, Raphael Mechoulam

^*Corresponding author for this work

School of Pharmacy

Research output: Contribution to journal › Article › peer-review

6 Scopus citations

Abstract

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).

Original language	English
Pages (from-to)	1797-1798
Number of pages	2
Journal	Journal of Heterocyclic Chemistry
Volume	17
Issue number	8
DOIs	https://doi.org/10.1002/jhet.5570170834
State	Published - Dec 1980

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title = "Structure elucidation of a condensation product of 4‐aminopyrrole derivatives and dicyclohexylcarbodiimide",

abstract = "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).",

author = "Meir Bialer and Boris Yagen and Raphael Mechoulam",

year = "1980",

month = dec,

doi = "10.1002/jhet.5570170834",

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volume = "17",

pages = "1797--1798",

journal = "Journal of Heterocyclic Chemistry",

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publisher = "John Wiley and Sons Inc.",

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AU - Bialer, Meir

AU - Yagen, Boris

AU - Mechoulam, Raphael

PY - 1980/12

Y1 - 1980/12

N2 - 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).

AB - 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).

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DO - 10.1002/jhet.5570170834

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AN - SCOPUS:0019176806

SN - 0022-152X

VL - 17

SP - 1797

EP - 1798

JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

IS - 8

ER -

Structure elucidation of a condensation product of 4‐aminopyrrole derivatives and dicyclohexylcarbodiimide

Abstract

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