861872-87-9Relevant academic research and scientific papers
Total synthesis of uniflorine A, casuarine, australine, 3-epi-australine, and 3,7-di-epi-australine from a common precursor
Ritthiwigrom, Thunwadee,Willis, Anthony C.,Pyne, Stephen G.
supporting information; experimental part, p. 815 - 824 (2010/06/15)
(Chemical Equation Presented) Aflexible method for the diastereoselective total synthesis of the pyrrolizidine alkaloids uniflorine A, casuarine, australine, and 3-epi-australine and the unnatural epimer 3,7-di-epi-australine from a common chiral 2,5-dihydropyrrole precursor is described. 2009 American Chemical Society.
Polyhydroxylated pyrrolizidines. Part 6: A new and concise stereoselective synthesis of (+)-casuarine and its 6,7-diepi isomer, from DMDP
Izquierdo, Isidoro,Plaza, María T.,Tamayo, Juan A.
, p. 6527 - 6533 (2007/10/03)
A new synthesis for (+)-casuarine (1) and its 6,7-diepi isomer (15) in a stereocontrolled manner, is reported herein. An appropriately protected polyhydroxylated pyrrolidine, such as (2R,3R,4R,5R)-3,4-dibenzyloxy-2′-O- tert-butyldiphenylsilyl-2,5-bis(hydr
