Microwave-assisted RCM for the synthesis of carbocyclic peptides

Elaridi, Jomana; Robinson, Andrea J.; Mujcinovic, Selma; Jackson, W. Roy; Van Lierop, Bianca J.

Microwave-assisted RCM for the synthesis of carbocyclic peptides

Elaridi, Jomana; Robinson, Andrea J.; Mujcinovic, Selma; Jackson, W. Roy; Van Lierop, Bianca J.

URI: http://hdl.handle.net/10725/2866

URL: http://onlinelibrary.wiley.com/doi/10.1002/psc.840/abstract

DOI: http://dx.doi.org/10.1002/psc.840

Date: 2015-12-22

Abstract:

Microwave irradiation dramatically improves the efficiency of ring closing metathesis (RCM) reactions of resin-attached peptides and the technology is illustrated by the highly selective synthesis of dicarba analogues of α-conotoxin IMI. Copyright  2007 European Peptide Society and John Wiley & Sons, Ltd.

Citation:

Robinson, A. J., Elaridi, J., Van Lierop, B. J., Mujcinovic, S., & Jackson, W. R. (2007). Microwave-assisted RCM for the synthesis of carbocyclic peptides. Journal of Peptide Science, 13(4), 280.