2012
DOI: 10.1002/chin.201209031
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: Ring Closure Reactions of 2,6‐Diazaheptatrienyl Metal Compounds: Synthesis of 3‐Aminoindole Derivatives and 14‐Membered Macrocyclic Dimers.

Abstract: Ring Closure Reactions of 2,6-Diazaheptatrienyl Metal Compounds: Synthesis of 3-Aminoindole Derivatives and 14-Membered Macrocyclic Dimers. -In dilute solution, potassium salts of diimines of type (I) undergo intramolecular cyclization to afford 3-aminoindoles. In more concentrated solution they undergo dimerization to 14-membered N-heterocycles. The vinylogous analogue (IX) provides the δ-carboline (X) under dilute conditions. -(NEUE, B.; REIERMANN, R.; GERDES, K.; FROEHLICH, R.; WIBBELING, B.; WUERTHWEIN*, E… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
0
0

Publication Types

Select...

Relationship

0
0

Authors

Journals

citations
Cited by 0 publications
references
References 1 publication
0
0
0
Order By: Relevance

No citations

Set email alert for when this publication receives citations?