A tandem metathesis–hydrogenation route to dicarba analogues of cystine-containing cyclic peptides

Elaridi, Jomana; Whelan, Amanda N.; Harte, Michael; Smith, Suzanne V.; Jackson, W. Roy; Robinson, Andrea J.

dc.creator	Elaridi, Jomana	en_US
dc.creator	Whelan, Amanda N.	en_US
dc.creator	Harte, Michael	en_US
dc.creator	Smith, Suzanne V.	en_US
dc.creator	Jackson, W. Roy	en_US
dc.creator	Robinson, Andrea J.	en_US
dc.date.accessioned	2015-12-22T09:38:33Z
dc.date.available	2015-12-22T09:38:33Z
dc.date.datecopyrighted	2004
dc.date.issued	2015-12-22
dc.identifier.issn	0040-4039	en_US
dc.identifier.uri	http://hdl.handle.net/10725/2870
dc.description.abstract	Dicarba cyclic peptide analogues of the cyclic peptide octreotide have been synthesised in good yields using a single pot, on resin, tandem homogeneous metal-catalysed metathesis–hydrogenation sequence.	en_US
dc.language.iso	en	en_US
dc.title	A tandem metathesis–hydrogenation route to dicarba analogues of cystine-containing cyclic peptides	en_US
dc.type	Article	en_US
dc.description.version	Published	en_US
dc.creator.school	SAS	en_US
dc.creator.identifier	201100947	en_US
dc.author.woa	N/A	en_US
dc.creator.department	Natural Sciences	en_US
dc.description.embargo	N/A	en_US
dc.relation.ispartof	Tetrahedron Letters	en_US
dc.description.volume	45	en_US
dc.description.issue	52	en_US
dc.article.pages	9545-9547	en_US
dc.keywords	Metathesis	en_US
dc.keywords	Hydrogenation	en_US
dc.keywords	Octreotide	en_US
dc.keywords	Tandem reactions	en_US
dc.identifier.doi	http://dx.doi.org/10.1016/j.tetlet.2004.10.165	en_US
dc.identifier.ctation	Whelan, A. N., Elaridi, J., Harte, M., Smith, S. V., Jackson, W. R., & Robinson, A. J. (2004). A tandem metathesis–hydrogenation route to dicarba analogues of cystine-containing cyclic peptides. Tetrahedron letters, 45(52), 9545-9547.	en_US
dc.creator.email	jomana.aridi@lau.edu.lb
dc.identifier.url	http://www.sciencedirect.com/science/article/pii/S004040390402427X