An efficient method for the preparation of N,N-disubstituted 1,2-diamines

Judith M Mitchell , Nathaniel S Finney

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Paper Details

DOI 10.1016/s0040-4039(00)01501-x

Journal Tetrahedron Letters
Location p 8431-8434, Volume 41, Issue 44, 2000
Publication Type journal-article

Tags chiral diamines, asymmetric synthesis, chiral ligands, organic chemistry, biochemistry, drug discovery
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Review

18 Feb 2017

Anonymous

(9)

Good synthesis with comments for improvement

Reproducibility

Clarity

Versatility

Innovation

The article presents a synthetic methodology to prepare chiral N,N-disubstituted, 1,2-diamines, which can be convenient precursors to tridentate ligands.

Particularly, I used the synthetic route using cyclohexane-1,2-diamine (both racemic and enatiopure) to obtain a series,...

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An efficient method for the preparation of N,N-disubstituted 1,2-diamines

Judith M Mitchell , Nathaniel S Finney

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Good synthesis with comments for improvement

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