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dc.contributor.authorKotha, Sambasivarao-
dc.contributor.authorKhedkar, Priti-
dc.date.accessioned2008-04-01T10:35:44Z-
dc.date.available2008-04-01T10:35:44Z-
dc.date.issued2007-06-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/632-
dc.description975-979en_US
dc.description.abstractConformationally 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.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.46B(6) [June 2007]en_US
dc.subjectPeptidomemiticsen_US
dc.subjectConformationally constrained amino acidsen_US
dc.subjectConformationally constrained imino acidsen_US
dc.subjectRing-closing metathesisen_US
dc.titleSynthesis of conformationally constrained ⍺-imino acid derivatives via ring-closing metathesisen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.46B(06) [June 2007]

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