Cho, YS Kang, KH Cha, JH Choi, KI Pae, AN Koh, HY Chang, MH 2024-01-21T10:05:22Z 2024-01-21T10:05:22Z 2021-09-01 2002-09-20 0253-2964 https://pubs.kist.re.kr/handle/201004/139206 Various nitrobenzaldehydes were simultaneously allylated and reduced using indium in the presence of HCl in aqueous media to give compounds having both functionality of homoallylic alcohol and aromatic amine. Sequential protection of the amino group and oxidation of the anilinyl homoallylic alcohol provided useful precursors of heterocyclic compounds such as dihydroindolones and dihydroquinolones, which could be efficiently synthesized through intramolecular cyclization reaction. English KOREAN CHEMICAL SOC AQUEOUS-MEDIA ORGANIC-REACTIONS A facile one-pot operations of reduction and allylation of nitrobenzaldehydes mediated by indium and their applications Article 1 BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.23, no.9, pp.1285 - 1290 BULLETIN OF THE KOREAN CHEMICAL SOCIETY 23 9 1285 1290 scie scopus kci ART001190432 000178759200024 2-s2.0-0037145157 Chemistry, Multidisciplinary Chemistry Article AQUEOUS-MEDIA ORGANIC-REACTIONS simultaneous reduction-allylation indium aqueous media