DIASTEREOSELECTIVE REACTION OF (1S,2S)-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL WITH AROMATIC ALDEHYDES. SYNTHESIS OF (1R,2R,4S,5S,8S)-2,8-DIARYL-4-(4-NITROPHENYL)-1-AZA-3,7-DIOXABICYCLO[3.3.0]OCTANES
DOI:
https://doi.org/10.1007/7988Keywords:
(1S, 2S)-2-amino-1-(4-nitrophenyl)-1, 3-propanediol, (1R, 2R, 4S, 5S, 8S)-2, 8-diaryl-4-(4-nitrophenyl)-1-aza-3, 7-dioxabicyclo[3.3.0]octane, oxazolidine, diastereoselectivity, 1H NMRAbstract
We have synthesized a series of (1R,2R,4S,5S,8S)-2,8-diaryl-4-(4-nitrophenyl)-1-aza-3,7-dioxabicyclo[3.3.0]octanes as a result of reaction of (1S,2S)-2-amino-1-(4-nitrophenyl)-1,3-propanediol with aromatic aldehydes. The structure of the compounds obtained was established on the basis of 1H NMR data.How to Cite
Madesclaire, M.; Coudert, P.; Gaumet, V.; Zaitsev, V. P.; Zaitseva, Yu. V. Chem. Heterocycl. Compd. 2006, 42, 665. [Khim. Geterotsikl. Soedin. 2006, 757.]
For this article in the English edition, see DOI 10.1007/s10593-006-0143-x