70561-78-3Relevant academic research and scientific papers
Synthesis of (+/-)-Allosedamine by Iodide Treatment of Isoxazolidinium Salts
Liguori, Angelo,Ottana, Rosaria,Romeo, Giovanni,Sindona, Giovanni,Uccella, Nicola
, p. 2019 - 2020 (2007/10/02)
A simple stereospecific route to the (+/-)-allosedamine alkaloid has been accomplished by ring opening of the isoxazolidinium salt 2 with lithium iodide. - Key Words: (+/-)-Allosedamine / 1,3-Dipolar cycloaddition / Five-membered ring opening / Isoxazolid
THE CYCLOADDITION REACTION BETWEEN STYRENE AND 2,3,4,5-TETRAHYDROPYRIDINE 1-OXIDE
Hootele, C.,Ibebeke-Bomangwa, W.,Driessens, F.,Sabil, S.
, p. 57 - 62 (2007/10/02)
The cycloaddition of styrene to 2,3,4,5-tetrahydropyridine 1-oxide leads, with a high yield, to a 97:3 mixture of the diastereoisomeric isoxazolidines 3c and 4c respectively.
