Molecular editing and biological evaluation of amphidinolide X and Y

A Fürstner, E Kattnig, G Kelter…

Index: Fuerstner, Alois; Kattnig, Egmont; Kelter, Gerhard; Fiebig, Heinz-Herbert Chemistry - A European Journal, 2009 , vol. 15, # 16 p. 4030 - 4043

Full Text: HTML

Citation Number: 25

Abstract

Abstract Scarce and precious: A collection of compounds with deep-seated structural “point mutations” within the framework of the marine natural products amphidinolide X and Y was prepared by “diverted total synthesis”. The resulting products provided first insights into the cytotoxicity profile of these extremely scarce macrolides.

Related Articles:

Novel Regioselective Ester Hydrolysis by Pig-Liver Esterase.

[Basak, Amit; Bhattacharya, Gautam; Palit, Sunanda K. Bulletin of the Chemical Society of Japan, 1997 , vol. 70, # 10 p. 2509 - 2513]

A Reformatsky Reagent. CC Bonds Formation by Substitution Reactions

[Orsini, F.; Pelizzoni, F. Synthetic Communications, 1983 , vol. 13, # 6 p. 523 - 530]

A Reformatsky Reagent. CC Bonds Formation by Substitution Reactions

[Orsini, F.; Pelizzoni, F. Synthetic Communications, 1983 , vol. 13, # 6 p. 523 - 530]

More Articles...