445246-22-0Relevant academic research and scientific papers
Amphimedosides A-C: Synthesis, chemoselective glycosylation, and biological evaluation
Langenhan, Joseph M.,Mullarky, Edouard,Rogalsky, Derek K.,Rohlfing, James R.,Tjaden, Anja E.,Werner, Halina M.,Rozal, Leonardo M.,Loskot, Steven A.
, p. 1670 - 1676 (2013/03/28)
The amphimedosides, discovered in 2006, are the first examples of naturally occurring glycosylated alkoxyamines. We report syntheses of amphimedosides A-C that feature a stereoselective oxyamine neoglycosylation and found that these alkaloids display mode
Total synthesis of cytotoxic sponge alkaloids hachijodines F and G
Goundry, William R. F.,Baldwin, Jack E.,Lee, Victor
, p. 1719 - 1729 (2007/10/03)
The total synthesis of two cytotoxic sponge alkaloids hachijodines F and G has been achieved. The synthesis of both compounds utilises a common intermediate alkyne. By comparison of spectra the structure of the natural product has been confirmed.
Total synthesis of cytotoxic sponge alkaloids hachijodines F and G
Goundry, William R.F.,Lee, Victor,Baldwin, Jack E.
, p. 2745 - 2747 (2007/10/03)
The total synthesis of two cytotoxic sponge alkaloids hachijodines F (1) and G (2) via a common intermediate 3 is described.
