Microwave-assisted RCM for the synthesis of carbocyclic peptides

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

dc.creator	Elaridi, Jomana	en_US
dc.creator	Robinson, Andrea J.	en_US
dc.creator	Mujcinovic, Selma	en_US
dc.creator	Jackson, W. Roy	en_US
dc.creator	Van Lierop, Bianca J.	en_US
dc.date.accessioned	2015-12-22T07:56:55Z
dc.date.available	2015-12-22T07:56:55Z
dc.date.datecopyrighted	2007
dc.date.issued	2015-12-22
dc.identifier.issn	1075-2617	en_US
dc.identifier.uri	http://hdl.handle.net/10725/2866
dc.description.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.	en_US
dc.language.iso	en	en_US
dc.title	Microwave-assisted RCM for the synthesis of carbocyclic 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.author.division	jomana.aridi@lau.edu.lb
dc.relation.ispartof	Journal of Peptide Science	en_US
dc.description.volume	13	en_US
dc.article.pages	280-285	en_US
dc.keywords	Microwave	en_US
dc.keywords	Ring closing metathesis	en_US
dc.keywords	icarba peptides	en_US
dc.keywords	Conotoxins	en_US
dc.identifier.doi	http://dx.doi.org/10.1002/psc.840
dc.identifier.ctation	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.	en_US
dc.identifier.url	http://onlinelibrary.wiley.com/doi/10.1002/psc.840/abstract