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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Mallakpour, Shadpour E | - |
| dc.contributor.author | Zolfigol, Mohammad Ali | - |
| dc.date.accessioned | 2013-03-27T19:48:48Z | - |
| dc.date.available | 2013-03-27T19:48:48Z | - |
| dc.date.issued | 1999-07 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16506 | - |
| dc.description | 777-782 | en_US |
| dc.description.abstract | Diels-Alder adducts of 4-substituted triazolinediones (4-Ph, 4-n-Pr) with cyclopellladienes have heen reacted with chlorine in carbon tetrachloride. When R = Ph only, cis-dichloride adduct is obtained in a stereos pecific manner. However, when R = n-Pr, two products, the cis-dichloride adduct and the rearrangement adduct are obtained in a stereoselective manner. The adducts of these triazolinediones with 1,3-cyclohexadiene have also been reacted with chlorine. When R = Ph, the trans-dichloride is formed with a high degree of stereoselectivity (98%). However, when R = n-Pr, two products, the trans-dichloride and the rearrangement adduct are obtained in 4:1 ratio. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights |  CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-B Vol.38B(07) [July 1999] | en_US |
| dc.title | Stereoselective chlorination of non-conjugated heterocyclic alkenes | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.38B(07) [July 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 38B(7) 777-782.pdf | 1.19 MB | Adobe PDF | View/Open |
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