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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kotha, Sambasivarao | - |
| dc.contributor.author | Khedkar, Priti | - |
| dc.date.accessioned | 2008-04-01T10:35:44Z | - |
| dc.date.available | 2008-04-01T10:35:44Z | - |
| dc.date.issued | 2007-06 | - |
| dc.identifier.issn | 0376-4699 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/632 | - |
| dc.description | 975-979 | en_US |
| dc.description.abstract | Conformationally constrained amino acid derivatives are useful in the synthesis of peptidomimetics. Seven-, and eight-membered conformationally constrained ⍺-imino acid derivatives have been prepared via RCM (ring-closing metathesis). Interestingly, attempts to achieve the synthesis of nine-membered imino acid derivative resulted in the formation of dimeric, 18-membered macrocyclic bis-⍺-imino acid derivative. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.source | IJCB Vol.46B(6) [June 2007] | en_US |
| dc.subject | Peptidomemitics | en_US |
| dc.subject | Conformationally constrained amino acids | en_US |
| dc.subject | Conformationally constrained imino acids | en_US |
| dc.subject | Ring-closing metathesis | en_US |
| dc.title | Synthesis of conformationally constrained ⍺-imino acid derivatives via ring-closing metathesis | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.46B(06) [June 2007] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 46B(6) (2007) 975-979.pdf | 111.48 kB | Adobe PDF | View/Open |
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