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http://nopr.niscpr.res.in/handle/123456789/632| Title: | Synthesis of conformationally constrained ⍺-imino acid derivatives via ring-closing metathesis |
| Authors: | Kotha, Sambasivarao Khedkar, Priti |
| Keywords: | Peptidomemitics;Conformationally constrained amino acids;Conformationally constrained imino acids;Ring-closing metathesis |
| Issue Date: | Jun-2007 |
| Publisher: | CSIR |
| 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. |
| Page(s): | 975-979 |
| ISSN: | 0376-4699 |
| 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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