1108750-53-3Relevant academic research and scientific papers
Exploring the original proposed biosynthesis of (+)-symbioimine: Remote exocyclic stereocontrol in a type i IMDA reaction
Burke, Jason P.,Sabat, Michal,Iovan, Diana A.,Myers, William H.,Chruma, Jason J.
supporting information; experimental part, p. 3192 - 3195 (2010/10/04)
(Figure Presented) The originally proposed biosynthesis of (+)-symbioimine was explored, resulting in the successful intramolecular Diels-Alder (IMDA) cyclization of an appropriate (E,E,E)-1,7,9-decatrien-3-one. In contrast to the originally proposed bios
Microwave-assisted intramolecular Diels-Alder reaction towards the total synthesis of symbioimine
Born, Stephen,Bacani, Genesis,Olson, Erin E.,Kobayashi, Yoshihisa
scheme or table, p. 2877 - 2881 (2009/05/07)
Uemura's proposed biosynthetic pathway of symbioimine was demonstrated by microwave-assisted intramolecular Diels-Alder reaction of a trans-enone precursor. Georg Thieme Verlag Stuttgart.
