A highly stereoselective route to medium-ring-sized trans-alkenolides via oxidative fragmentation of bicyclic oxycyclopropane precursors : application to the synthesis of (+)-recifeiolide

autor
vastutusandmed
Dzmitry M. Zubrytski, Dzmitry G. Kananovich, Oleg G. Kulinkovich
allikas
ajakirja aastakäik number kuu
Vol. 70, 18
ilmumisaasta
leheküljed
p. 2944-2950 : ill
ISSN
0040-4020
märkused
Bibliogr.: 33 ref
keel
inglise
võtmesõna
alkenolides
hypervalent iodine compounds
stereoselective synthesis
(+)-recifeiolide
TTÜ struktuuriüksus
Zubrytski, D.M., Kananovich, D.G., Kulinkovich, O.G. A highly stereoselective route to medium-ring-sized trans-alkenolides via oxidative fragmentation of bicyclic oxycyclopropane precursors : application to the synthesis of (+)-recifeiolide // Tetrahedron (2014) Vol. 70, 18, p. 2944-2950 : ill. https://www.sciencedirect.com/science/article/abs/pii/S0040402014003524