98260-55-0Relevant academic research and scientific papers
Dehydrogenation with Benzeneseleninic Anhydride in the Total Synthesis of Ergot Alkaloids
Ninomiya, Ichiya,Hashimoto, Chiyomi,Kiguchi, Toshiko,Naito, Takeaki,Barton, Derek, H. R.,et al.
, p. 707 - 713 (2007/10/02)
Investigation of the dehydrogenative conversion of indolines into indoles with benzeneseleninic anhydride (1) resulted in the development of an efficient standardised procedure, which was successfully applied to the final steps in first total synthesis of (+/-)-lysergol (18), (+/-)-isolysergol (27), and (+/-)-elymoclavine (29).
A TOTAL SYNTHESIS OF (+/-)-LYSERGOL, A 9-ERGOLENE TYPE OF ERGOT ALKALOID
Kiguchi, Toshiko,Hashimoto, Chiyomi,Ninomiya, Ichiya
, p. 1377 - 1380 (2007/10/02)
According to the synthetic route established on the despyrrole analog of the alkaloid, the first total synthesis of (+/-)-lysergol was completed.
