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
Publisher Link Click Here

Review

18 Feb 2017

Anonymous

(6)

Good synthesis with comments for improvement

Reproducibility

Clarity

Versatility

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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