Cyanuric Chloride-Catalyzed Michael Addition of Indoles to Nitroolefins under Solvent-Free Conditions
Cyanuric chloride is an inexpensive, efficient, and mild catalyst for the Michael addition of indoles to nitroolefins at 70°C under solvent-free conditions. The simple experimental procedure, solvent-free reaction conditions, utilization of an inexpensive and readily available catalyst, short period...
Saved in:
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wiley
2013-01-01
|
| Series: | Journal of Chemistry |
| Online Access: | http://dx.doi.org/10.1155/2013/429235 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| _version_ | 1850234282829676544 |
|---|---|
| author | Xiao Juan Yang Yun Jing |
| author_facet | Xiao Juan Yang Yun Jing |
| author_sort | Xiao Juan Yang |
| collection | DOAJ |
| description | Cyanuric chloride is an inexpensive, efficient, and mild catalyst for the Michael addition of indoles to nitroolefins at 70°C under solvent-free conditions. The simple experimental procedure, solvent-free reaction conditions, utilization of an inexpensive and readily available catalyst, short period of conversion, and excellent yields are the advantages of the present method. |
| format | Article |
| id | doaj-art-15c7690a3e714c65b8b14809bf8e5d75 |
| institution | OA Journals |
| issn | 2090-9063 2090-9071 |
| language | English |
| publishDate | 2013-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | Journal of Chemistry |
| spelling | doaj-art-15c7690a3e714c65b8b14809bf8e5d752025-08-20T02:02:40ZengWileyJournal of Chemistry2090-90632090-90712013-01-01201310.1155/2013/429235429235Cyanuric Chloride-Catalyzed Michael Addition of Indoles to Nitroolefins under Solvent-Free ConditionsXiao Juan Yang0Yun Jing1College of Chemistry and Chemical Engineering, Xinxiang University, Henan, Xinxiang 453003, ChinaSchool of Pharmacy, Xinxiang Medical University, Henan, Xinxiang 453003, ChinaCyanuric chloride is an inexpensive, efficient, and mild catalyst for the Michael addition of indoles to nitroolefins at 70°C under solvent-free conditions. The simple experimental procedure, solvent-free reaction conditions, utilization of an inexpensive and readily available catalyst, short period of conversion, and excellent yields are the advantages of the present method.http://dx.doi.org/10.1155/2013/429235 |
| spellingShingle | Xiao Juan Yang Yun Jing Cyanuric Chloride-Catalyzed Michael Addition of Indoles to Nitroolefins under Solvent-Free Conditions Journal of Chemistry |
| title | Cyanuric Chloride-Catalyzed Michael Addition of Indoles to Nitroolefins under Solvent-Free Conditions |
| title_full | Cyanuric Chloride-Catalyzed Michael Addition of Indoles to Nitroolefins under Solvent-Free Conditions |
| title_fullStr | Cyanuric Chloride-Catalyzed Michael Addition of Indoles to Nitroolefins under Solvent-Free Conditions |
| title_full_unstemmed | Cyanuric Chloride-Catalyzed Michael Addition of Indoles to Nitroolefins under Solvent-Free Conditions |
| title_short | Cyanuric Chloride-Catalyzed Michael Addition of Indoles to Nitroolefins under Solvent-Free Conditions |
| title_sort | cyanuric chloride catalyzed michael addition of indoles to nitroolefins under solvent free conditions |
| url | http://dx.doi.org/10.1155/2013/429235 |
| work_keys_str_mv | AT xiaojuanyang cyanuricchloridecatalyzedmichaeladditionofindolestonitroolefinsundersolventfreeconditions AT yunjing cyanuricchloridecatalyzedmichaeladditionofindolestonitroolefinsundersolventfreeconditions |