10.1021/ol201320v.s002
Gang Li
Gang
Li
Albert Padwa
Albert
Padwa
Intramolecular Diels–Alder Cycloaddition/Rearrangement Cascade of an Amidofuran Derivative for the Synthesis of (±)-Minfiensine
American Chemical Society
2011
MinfiensineAn
alkaloid
intramolecular
minfiensine
Thermal reorganization
cycloaddition
Diel
synthesis
tetrahydroiminoethanocarbazole skeleton
Amidofuran
Cascade
cycloadduct
Cycloaddition
amidofuran
cascade
Intramolecular
Synthesi
2011-08-05 00:00:00
Journal contribution
https://acs.figshare.com/articles/journal_contribution/Intramolecular_Diels_Alder_Cycloaddition_Rearrangement_Cascade_of_an_Amidofuran_Derivative_for_the_Synthesis_of_Minfiensine/2625580
An efficient synthesis of (±)-minfiensine has been accomplished employing an intramolecular Diels–Alder cycloaddition/rearrangement cascade of an amidofuran derivative. Thermal reorganization of the initially formed [4 + 2]-cycloadduct affords the critical tetrahydroiminoethanocarbazole skeleton of the alkaloid in high yield.