Abstract
An unprecedented route for the synthesis of 3,3′-biindoles is developed. Both symmetrical and unsymmetrical 3,3′-biindoles could be generated by this method. Mild conditions, high yields of the products, and environmentally acceptable reagent are the merits of the procedure.
| Original language | English |
|---|---|
| Pages (from-to) | 3796-3801 |
| Number of pages | 6 |
| Journal | European Journal of Organic Chemistry |
| Issue number | 20 |
| DOIs | |
| Publication status | Published - 2010 Jul 1 |
Fingerprint
Keywords
- Cyclization
- Iron
- Michael addition
- Nitroalkenes
- Nitrogen heterocycles
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry
Cite this
An unprecedented route for the synthesis of 3,3′-biindoles by reductive cyclization of 3-[2-Nitro-1-(2-nitrophenyl)ethyl]-1H-indoles mediated by iron/ acetic acid. / Ramesh, Chintakunta; Kavala, Veerababurao; Kuo, Chun Wei; Raju, B. Rama; Yao, Ching Fa.
In: European Journal of Organic Chemistry, No. 20, 01.07.2010, p. 3796-3801.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - An unprecedented route for the synthesis of 3,3′-biindoles by reductive cyclization of 3-[2-Nitro-1-(2-nitrophenyl)ethyl]-1H-indoles mediated by iron/ acetic acid
AU - Ramesh, Chintakunta
AU - Kavala, Veerababurao
AU - Kuo, Chun Wei
AU - Raju, B. Rama
AU - Yao, Ching Fa
PY - 2010/7/1
Y1 - 2010/7/1
N2 - An unprecedented route for the synthesis of 3,3′-biindoles is developed. Both symmetrical and unsymmetrical 3,3′-biindoles could be generated by this method. Mild conditions, high yields of the products, and environmentally acceptable reagent are the merits of the procedure.
AB - An unprecedented route for the synthesis of 3,3′-biindoles is developed. Both symmetrical and unsymmetrical 3,3′-biindoles could be generated by this method. Mild conditions, high yields of the products, and environmentally acceptable reagent are the merits of the procedure.
KW - Cyclization
KW - Iron
KW - Michael addition
KW - Nitroalkenes
KW - Nitrogen heterocycles
UR - http://www.scopus.com/inward/record.url?scp=77954302545&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77954302545&partnerID=8YFLogxK
U2 - 10.1002/ejoc.201000276
DO - 10.1002/ejoc.201000276
M3 - Article
AN - SCOPUS:77954302545
SP - 3796
EP - 3801
JO - Annalen der Pharmacie
JF - Annalen der Pharmacie
SN - 0075-4617
IS - 20
ER -