1 article(s) from Filo, Juraj
Ireland–Claisen rearrangement of allyl esters 1a–c.
Jump to Scheme 1
Ireland–Claisen rearrangement of 1c mediated by tertiary amines.
Jump to Scheme 2
Organocatalysts used in this study. Conditions: typical procedure: 1. Et3N (4.9 equiv), DCM, −60 °C...
Jump to Figure 1
Solvent-free Ireland–Claisen rearrangement of cinnamyl esters.
Jump to Scheme 3
ωB97X-D/6-31G* calculated uncatalyzed Ireland–Claisen rearrangement of 1c. Charges on allylic oxyge...
Jump to Figure 2
ωB97X-D/6-31G* calculated Schreiner thiourea (12)-catalyzed Ireland–Claisen rearrangement of 1c. Ch...
Jump to Figure 3
ωB97X-D/6-31G* calculated Ph-thiourea (top) and squaramide-catalyzed (bottom) Ireland–Claisen rearr...
Jump to Figure 4
a) Rate of product formation; b) reaction profile without catalyst determined by 1H NMR.
Jump to Figure 5
Beilstein J. Org. Chem. 2019, 15, 2948–2957, doi:10.3762/bjoc.15.290
Subscribe to our Latest Articles RSS Feed.
Register and get informed about new articles.
Follow the Beilstein-Institut