| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5217190 | Tetrahedron | 2014 | 6 Pages |
Abstract
Functionalized spiro-tetrahydro-β-carbolines were formed by an efficient gold(I)-catalyzed rearrangement reaction of alkynylaziridine indoles. The reaction involved a Friedel–Crafts type intramolecular reaction of alkynylaziridine indoles, following by hydroamination of aminoallene intermediate.
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