298713-13-0Relevant academic research and scientific papers
Pyranophane Transannular Diels-Alder Approach to (+)-Chatancin: A Biomimetic Asymmetric Total Synthesis
Soucy, Pierre,L'Heureux, Alexandre,Toro, Andras,Deslongchamps, Pierre
, p. 9983 - 9987 (2007/10/03)
An asymmetric total synthesis of (+)-chatancin was achieved via a transannular Diels-Alder (TADA) reaction of an in situ generated macrocyclic pyranophane pseudobase. The presented route constitutes the second of two proposed biosynthetic pathways that in
Transannular Diels-Alder studies on the asymmetric total synthesis of chatancin: the pyranophane approach.
Toro,L'Heureux,Deslongchamps
, p. 2737 - 2740 (2007/10/03)
[reaction: see text] A pathway is proposed for the biosynthesis of (+)-chatancin and (+)-sarcophytin linking these tetracycles to cembranoids by a pyranophane transannular Diels-Alder reaction. Preliminary synthetic results in this direction to reach macr
