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Please use this identifier to cite or link to this item:
http://hdl.handle.net/2074/1065
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Full metadata record
| DC Field | Value | Language |
| contributor.author | Arora, Vandna | - |
| contributor.author | Chawla, H M | - |
| contributor.author | Santra, Anuradha | - |
| date.accessioned | 2005-12-30T04:22:35Z | - |
| date.available | 2005-12-30T04:22:35Z | - |
| date.issued | 2002 | - |
| identifier.citation | Tetrahedron, 58(28), 5591-5597 | en |
| identifier.uri | http://eprint.iitd.ac.in/dspace/handle/2074/1065 | - |
| description.abstract | By careful choice of a catalyst (TiCl4 or SnCl4), temperature, reaction time and mole ratio of the substrate to dichloromethylmethylether, it has been possible to obtain new functionalized formylated calix[n]arenes in the cone or partial cone conformation. Optimized general reaction procedures for obtaining mono-, di-, tri- and tetraformylated derivatives of calix[4]arenes as exemplified by formylation of tetramethoxy-, tetrakis(2-ethoxyethoxy)-, bis(ethoxycarbonylmethoxy)- and bis(hexadecyloxy)-calix[4]-arenes have been reported. | en |
| format.extent | 71142 bytes | - |
| format.mimetype | application/pdf | - |
| language.iso | en | en |
| subject | selective | en |
| subject | calix[4]arene | en |
| subject | formylation | en |
| title | Synthesis of selectively formylated calixarene ethers | en |
| type | Article | en |
| Appears in Collections: | Chemistry
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| File |
Description |
Size | Format |
| arorasyn2002.pdf | | 69Kb | Adobe PDF | View/Open |
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