Articles citing this paper
Preparation of the Central Tryptophan Moiety of the Celogentin/Moroidin Family of Anti-Mitotic Cyclic Peptides
Alexander K. L. Yuen A , Katrina A. Jolliffe A and Craig A. Hutton B C
+ Author Affiliations
- Author Affiliations
A School of Chemistry, University of Sydney, Sydney NSW 2006, Australia.
B School of Chemistry and Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, Melbourne VIC 3010, Australia.
C Corresponding author. Email: chutton@unimelb.edu.au
Australian Journal of Chemistry 59(11) 819-826 https://doi.org/10.1071/CH06324
Submitted: 1 September 2006 Accepted: 2 October 2006 Published: 17 November 2006
15 articles found in Crossref database.
Heterocycles in Natural Product Synthesis (2011)
(2013)
Preparation of Cyclic Peptide Alkaloids Containing Functionalized Tryptophan Residues
Yuen Alexander K. L., Hutton Craig A.
Natural Product Communications. 2006 1(10). p.1934578X0600101
A critical review of the 2006 literature preceded by two chapters on current heterocyclic topics (2008)
Total Synthesis of the Antimitotic Bicyclic Peptide Celogentin C
Ma Bing,
Banerjee Biplab,
Litvinov Dmitry N.,
He Liwen, Castle Steven L.
Journal of the American Chemical Society. 2010 132(3). p.1159
Synthesis of the Leu - Trp Component of the Celogentin Family of Cyclic Peptides Through a C - H Activation - Cross-Coupling Strategy
Li Barbara T. Y.,
White Jonathan M., Hutton Craig A.
Australian Journal of Chemistry. 2010 63(3). p.438
Convenient and efficient synthesis of a lanthanide3+‐coordinated, diethylene triamine pentaacetic acid labeled biopolymer as an assay for the cholecystokinin B receptor
Gao F.,
Handl H.,
Vagner J.,
Hruby V., Gillies R.
Journal of Applied Polymer Science. 2007 106(4). p.2683
Muscarine, imidazole, oxazole and thiazole alkaloids
Jin Zhong
Natural Product Reports. 2009 26(3). p.382
Preparation of the Central Tryptophan Moiety (I) of the Celogentin/Moroidin Family of Antimitotic Cyclic Peptides.
Yuen Alexander K. L.,
Jolliffe Katrina A., Hutton Craig A.
ChemInform. 2007 38(17).
Stereocontrolled and Efficient Total Synthesis of (−)-Stephanotic Acid Methyl Ester and (−)-Celogentin C
Hu Weimin,
Zhang Fengying,
Xu Zhengren,
Liu Qiang,
Cui Yuxin, Jia Yanxing
Organic Letters. 2010 12(5). p.956
Development of novel derivatives of stilbene and macrocyclic compounds as potent of anti-microtubule factors
Borys Filip,
Tobiasz Piotr,
Poterała Marcin, Krawczyk Hanna
Biomedicine & Pharmacotherapy. 2021 133 p.110973
Total Synthesis of Celogentin C
Ma Bing,
Litvinov Dmitry N.,
He Liwen,
Banerjee Biplab, Castle Steven L.
Angewandte Chemie. 2009 121(33). p.6220
Total Synthesis of Celogentin C
Ma Bing,
Litvinov Dmitry N.,
He Liwen,
Banerjee Biplab, Castle Steven L.
Angewandte Chemie International Edition. 2009 48(33). p.6104
Bicyclic Peptides as Next‐Generation Therapeutics
Rhodes Curran A., Pei Dehua
Chemistry – A European Journal. 2017 23(52). p.12690
Synthetic studies of cyclic peptides stephanotic acid methyl ester, celogentin C, and moroidin
Li Lei,
Hu Weimin, Jia Yanxing
Tetrahedron. 2014 70(42). p.7753