132402-81-4Relevant articles and documents
Concise synthesis of stereodefined, thiazole - Containing cyclic hexa- and octapeptide relatives of the Lissoclinums, via cyclooligomerisation reactions
Bertram, Anna,Blake, Alexander J.,González-López De Turiso, Felix,Hannam, Jeffery S.,Jolliffe, Katrina A.,Pattenden, Gerald,Skae, Michael
, p. 6979 - 6990 (2003)
The synthesis of a range of thiazole containing cyclic peptides using cyclooligomerisation reactions of amino acid substituted thiazole monomers and by macrolactamisation procedures is reported. The synthetic approaches lead to high yields of novel 18- and 24-membered ring analogues of the naturally occurring Lissoclinum families of cyclic peptides found in marine organisms and algae.
Total Synthesis of Lissoclinamide 5, a Cytotoxic Cyclic Peptide from the Tunicate Lissoclinum patella
Boden, Christopher,Pattenden, Gerald
, p. 8271 - 8274 (2007/10/02)
A total synthesis of lissoclinamide 5, and some of its stereoisomers, shows that its stereostructure should be revised to 13.