Kotha, Sambasivarao ; Khedkar, Priti (2007) Synthesis of conformationally constrained α-imino acid derivatives via ring-closing metathesis Indian Journal of Chemistry - Section B: Organic and Medicinal Chemistry, 46 . pp. 975-979. ISSN 0376-4699
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Abstract
Conformationally constrained amino acid derivatives are useful in the synthesis of peptidomimetics. Seven-, and eight-membered conformationally constrained α-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-α-imino acid derivative.
Item Type: | Article |
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Source: | Copyright of this article belongs to National Institute of Science Communication and Information Resources. |
Keywords: | Peptidomemitics; Conformationally Constrained Amino Acids; Conformationally Constrained Imino Acids; Ring-closing Metathesis |
ID Code: | 65234 |
Deposited On: | 15 Oct 2011 11:45 |
Last Modified: | 18 May 2016 13:19 |
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