52574-63-7Relevant academic research and scientific papers
Divergent Access to Histone Deacetylase Inhibitory Cyclopeptides via a Late-Stage Cyclopropane Ring Cleavage Strategy. Short Synthesis of Chlamydocin
Elek, Gábor Zoltán,Koppel, Kaur,Zubrytski, Dzmitry M.,Konrad, Nele,J?rving, Ivar,Lopp, Margus,Kananovich, Dzmitry G.
supporting information, p. 8473 - 8478 (2019/10/16)
A unified step-economical strategy for accessing histone deacetylase inhibitory peptides is proposed, based on the late-stage installation of multiple zinc-binding functionalities via the cleavage of the strained cyclopropane ring in the common pluripoten
Synthesis of the cytostatic cyclic tetrapeptide, chlamydocin
Rich,Gardner
, p. 5305 - 5308 (2007/10/02)
Chlamydocin has been synthesized by a route utilizing allylic hydroxylation and epoxidation of the DL-2-amino-9-decenoic acid residue to form the 2-amino-8-oxo-9,10-epoxydecanoic acid residue.
AMINOSAEUREN UND PEPTIDE - XXXXII. SYNTHESE VON CHLAMYDOCIN + EPI-CHLAMYDOCIN
Schmidt, Von Ulrich,Beuttler, Thomas,Lieberknecht, Albrecht,Griesser, Helmut
, p. 3573 - 3576 (2007/10/02)
The total synthesis of the cytostatic Chlamydocin together with his diastereomer epi-Chlamydocin is described.
