Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/30689Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Jin, Tong-Shou | - |
| dc.contributor.author | Zhao, Rui-Qiao | - |
| dc.contributor.author | Ma, Yen-Ran | - |
| dc.contributor.author | Yang, Mi-Na | - |
| dc.contributor.author | Guo, Jun-Jic | - |
| dc.contributor.author | Li, Tong-Shuang | - |
| dc.date.accessioned | 2015-02-26T11:45:08Z | - |
| dc.date.available | 2015-02-26T11:45:08Z | - |
| dc.date.issued | 2006-02 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/30689 | - |
| dc.description | 503-505 | en_US |
| dc.description.abstract | Formation of 1,3-oxathiolanes from aldehydes and ketones using 2-mercaptoethanol in the presence of TiCl4-montmorillonite under mild reaction conditions in excellent yields is described. Chernoselective monothioacetalization of aldehyde in the presence of ketone can also he achieved in high yield. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.relation.ispartofseries | Int.CI.7 C 07 D | en_US |
| dc.rights |  CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-B Vol.45B(02) [February 2006] | en_US |
| dc.subject | 1,3-oxathiolanes | en_US |
| dc.subject | Aldehydes | en_US |
| dc.subject | Ketones | en_US |
| dc.subject | Chemoselective | en_US |
| dc.subject | 2-mercaptoethanol | en_US |
| dc.subject | Conversion | en_US |
| dc.title | An efficient and chemoselective method for conversion of carbonyl compounds to 1,3-oxathiolanes with 2-mercaptoethanol catalyzed by TiCl4-montmorillonitc | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.45B(02) [February 2006] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 45B(2) 503-505.pdf | 585.23 kB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.