Hideki Abe

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Organization: Tokyo University of Pharmacy and Life Sciences
Department: School of Life Sciences
Title:
Co-reporter:Hideki Abe, Naohiro Miyagawa, Sho Hasegawa, Toyoharu Kobayashi, Sakae Aoyagi, Chihiro Kibayashi, Tadashi Katoh, Hisanaka Ito
Tetrahedron Letters 2015 Volume 56(Issue 7) pp:921-924
Publication Date(Web):11 February 2015
DOI:10.1016/j.tetlet.2014.12.130
Synthesis of 2-spiroindolines from 2-substituted indole derivatives via acid-induced N-acyliminium ion-conjugated diene spirocyclization was demonstrated. This methodology can be used to direct transformations of 2-substituted indole moieties into 3-nonsubstituted-2-spiroindoline skeletons.
Propanoic acid, 2-(diphenoxyphosphinyl)-, ethyl ester
2-Cyclohepten-1-one, 4-(benzoyloxy)-
SILANE, [(4-BROMO-4-PENTENYL)OXY](1,1-DIMETHYLETHYL)DIMETHYL-
Methyl 4-((tert-butyldimethylsilyl)oxy)but-2-ynoate
Silanamine, N-(2,4-dimethylphenyl)-1,1,1-trimethyl-
Magnesium, bromo(3-methyl-3-butenyl)-