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Article: Peptides of aminoxy acids as foldamers

TitlePeptides of aminoxy acids as foldamers
Authors
Issue Date2006
PublisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/Publishing/Journals/cc/index.asp
Citation
Chemical Communications, 2006 n. 32, p. 3367-3379 How to Cite?
AbstractThis Feature Article summarizes our efforts in developing a new family of foldamers from α-, β- and γ-aminoxy acids. From a series of conformational studies, we demonstrate that peptides consisting of aminoxy acids adopt several well-defined secondary structures, such as α N-O turns (which feature an eight-membered-ring hydrogen bond), β N-O turns (a nine-membered-ring hydrogen bond), γ N-O turns (a ten-membered-ring hydrogen bond), 1.88 helices (consecutive homochiral α N-O turns), 7/8 helices (alternating α N-O turns and γ-turns), 1.7 9 helices (consecutive β N-O turns), reverse turns (consecutive heterochiral α N-O turns) and sheet-like structures. © The Royal Society of Chemistry 2006.
Persistent Identifierhttp://hdl.handle.net/10722/68911
ISSN
2015 Impact Factor: 6.567
2015 SCImago Journal Rankings: 2.771
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorLi, Xen_HK
dc.contributor.authorYang, Den_HK
dc.date.accessioned2010-09-06T06:08:50Z-
dc.date.available2010-09-06T06:08:50Z-
dc.date.issued2006en_HK
dc.identifier.citationChemical Communications, 2006 n. 32, p. 3367-3379en_HK
dc.identifier.issn1359-7345en_HK
dc.identifier.urihttp://hdl.handle.net/10722/68911-
dc.description.abstractThis Feature Article summarizes our efforts in developing a new family of foldamers from α-, β- and γ-aminoxy acids. From a series of conformational studies, we demonstrate that peptides consisting of aminoxy acids adopt several well-defined secondary structures, such as α N-O turns (which feature an eight-membered-ring hydrogen bond), β N-O turns (a nine-membered-ring hydrogen bond), γ N-O turns (a ten-membered-ring hydrogen bond), 1.88 helices (consecutive homochiral α N-O turns), 7/8 helices (alternating α N-O turns and γ-turns), 1.7 9 helices (consecutive β N-O turns), reverse turns (consecutive heterochiral α N-O turns) and sheet-like structures. © The Royal Society of Chemistry 2006.en_HK
dc.languageengen_HK
dc.publisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/Publishing/Journals/cc/index.aspen_HK
dc.relation.ispartofChemical Communicationsen_HK
dc.titlePeptides of aminoxy acids as foldamersen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1359-7345&volume=&spage=3367&epage=3379&date=2006&atitle=Peptides+of+aminoxy+acids+as+foldamers+en_HK
dc.identifier.emailLi, X:xiangli@hku.hken_HK
dc.identifier.emailYang, D:yangdan@hku.hken_HK
dc.identifier.authorityLi, X=rp01562en_HK
dc.identifier.authorityYang, D=rp00825en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/b602230hen_HK
dc.identifier.pmid16896469-
dc.identifier.scopuseid_2-s2.0-33746888291en_HK
dc.identifier.hkuros122157en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-33746888291&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.issue32en_HK
dc.identifier.spage3367en_HK
dc.identifier.epage3379en_HK
dc.identifier.isiWOS:000239639700001-
dc.publisher.placeUnited Kingdomen_HK
dc.identifier.scopusauthoridLi, X=49761544200en_HK
dc.identifier.scopusauthoridYang, D=7404800756en_HK

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