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Intramolecular oxidative diamination and aminohydroxylation of olefins under metal-free conditions SCIE SCOPUS

Title
Intramolecular oxidative diamination and aminohydroxylation of olefins under metal-free conditions
Authors
Kim, HJCho, SHChang, S
Date Issued
2012-03-16
Publisher
American Chemical Society
Abstract
A metal-free procedure that is simple to operate and convenient to handle was developed for the facile intramolecular oxidative diamination of olefins using an iodobenzene diacetate oxidant and a halide additive to furnish bisindolines at room temperature. The present reaction is featured by mild conditions, a broad substrate scope, and excellent functional group tolerance. The same protocol was successfully extended to the aminohydroxylation.
Keywords
N BOND FORMATION; ACTIVATED METHYLENE-COMPOUNDS; C-H BONDS; CONJUGATED DIENES; STEREOSELECTIVE-SYNTHESIS; MECHANISTIC PATHWAYS; HYPERVALENT IODINE; DIRECT AMINATION; ALKENES; CYCLIZATION
URI
https://oasis.postech.ac.kr/handle/2014.oak/14436
DOI
10.1021/OL300166Q
ISSN
1523-7060
Article Type
Article
Citation
ORGANIC LETTERS, vol. 14, no. 6, page. 1424 - 1427, 2012-03-16
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