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

full record print

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

author

Zubrytski, Dzmitry

Kananovich, Dzmitry

Kulinkovich, Oleg

statement of authorship

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

source

Tetrahedron

journal volume number month

Vol. 70, 18

year of publication

2014

pages

p. 2944-2950 : ill

url

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

ISSN

0040-4020

notes

Bibliogr.: 33 ref

language

inglise

Märksõnad ja võtmesõnad

subject term

orgaanilised ühendid

stereoselektiivne süntees

keyword

alkenolides

cyclopropanols

hypervalent iodine compounds

stereoselective synthesis

(+)-recifeiolide

TalTechi üksused

TTÜ department

keemiainstituut

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