Fig. 2: Substrate scope of 1,1-disubstituted alkenes and azodicarboxylates.
From: Enantioselective aza-electrophilic dearomatization of naphthalene derivatives
Yields are for isolated and purified products. e.r. is determined by HPLC analysis. See the supplementary materials for detailed procedures. a The reaction was carried out at −78 °C ~ −20 °C. Fmoc 9-fluorenylmethyloxycarbonyl, Troc 2,2,2-trichloroethoxycarbonyl, MOM methoxyethyl.
