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http://nopr.niscpr.res.in/handle/123456789/22453Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Rajesh, S | - |
| dc.contributor.author | Srivastava, Jyoti | - |
| dc.contributor.author | Banerji, Biswadip | - |
| dc.contributor.author | Iqbal, Javed | - |
| dc.date.accessioned | 2013-10-22T11:19:03Z | - |
| dc.date.available | 2013-10-22T11:19:03Z | - |
| dc.date.issued | 2001-11 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/22453 | - |
| dc.description | 1029-1032 | en_US |
| dc.description.abstract | α-Dehydro β-amino
acid derivatives
derived di- and tripeptides 4-7 adopt eight-member turn conformations in
CDCl3 solutions. These peptides show similar hydrogen bonding
characterstics as compared to the corresponding  -proline containing peptides 8. Thus the dehydro
β-amino acid
derived tripeptides 7 may behave as the structural mimic of the -proline containing tripeptides
8c which are structural analogues of HIV protease inhibitors. | 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.40B(11) [November 2001] | en_US |
| dc.title | α-Dehydro β-amino acid derivatives as turn inducer: Synthesis of potential HIV protease inhibitors based on structural mimicry† | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.40B(11) [November 2001] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 40B(11) 1029-1032.pdf | 738.53 kB | Adobe PDF | View/Open |
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