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.

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.

URI: http://hdl.handle.net/10725/2870

URL: http://www.sciencedirect.com/science/article/pii/S004040390402427X

DOI: http://dx.doi.org/10.1016/j.tetlet.2004.10.165

Date: 2015-12-22

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.

Citation:

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.