Efficient synthesis of the gadolinium complex of a new C2-symmetric tetramine
β Scribed by Michael Harre; Klaus Nickisch; Claudia Schulz; Hilmar Weinmann
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 203 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A short and efficient synthesis of the substituted tetramines 2a and 7 and of the gadolinium complex 1 was developed starting from the Cbz-protected amino alcohol 3. Key steps of the synthesis are the optimized bleach oxidation of enantiopure alcohols and the bridging of the resulting aldehyde molecules by double reductive amination with ethylenediamine. Interesting biological activity of the amines 2a and 7 was detected.
π SIMILAR VOLUMES
The oxidation of a C 2 symmetric piperidine, obtained through a ring enlargement process of the enantiopure protected (4R)-hydroxy-(2S)-hydroxymethyl pyrrolidine, is reported. Oxidation with C-phenyl-N-phenylsulfonyloxaziridine afforded the corresponding nitrone that is too unstable for isolation an