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Wiley-VCH Verlag, ChemInform, 50(43), p. no-no, 2012

DOI: 10.1002/chin.201250064

Wiley, Angewandte Chemie International Edition, 28(51), p. 7031-7034, 2012

DOI: 10.1002/anie.201201719

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Palladium-Catalyzed Vicinal Difunctionalization of Internal Alkenes: Diastereoselective Synthesis of Diamines

Journal article published in 2012 by Claudio Martínez ORCID, Kilian Muñiz ORCID
This paper is available in a repository.
This paper is available in a repository.

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Abstract

Internal affairs: the first general palladium-catalyzed intermolecular diamination of internal alkenes employs different nitrogen sources, which add to the alkene in a regio- and diastereoselective fashion. The resulting diamination products can be converted directly into a known ligand motif.