Zubrytski, D.M., Kananovich, D.G., Kulinkovich, O.G.

prindi

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

autor

Zubrytski, Dzmitry

Kananovich, Dzmitry

Kulinkovich, Oleg

vastutusandmed

Dzmitry M. Zubrytski, Dzmitry G. Kananovich, Oleg G. Kulinkovich

allikas

Tetrahedron

ajakirja aastakäik number kuu

Vol. 70, 18

ilmumisaasta

2014

leheküljed

p. 2944-2950 : ill

leitav

https://www.sciencedirect.com/science/article/abs/pii/S0040402014003524

märksõna

orgaanilised ühendid

stereoselektiivne süntees

võtmesõna

alkenolides

cyclopropanols

hypervalent iodine compounds

stereoselective synthesis

(+)-recifeiolide

ISSN

0040-4020

märkused

Bibliogr.: 33 ref

TTÜ struktuuriüksus

keemiainstituut

keel

inglise

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