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Blum-Ittah aziridine synthesis

Ring opening of oxiranes using azide followed by PPI13 reduction of the intermediate azido alcohol to give the corresponding aziridines. Cf. Staudinger reduction. [Pg.60]

Regardless of the regioselectivity of the Sn2 reaction of the azide, the ultimate stereochemieal outcome for the aziridine is the same. [Pg.60]

Name Reactions A Collection of Detailed Mechanisms and Synthetic Applications, DOI 10.1007/978-3-319-03979-4 29, Springer International Publisbing Switzerland 2014 [Pg.60]

Sasson, Y. Shahak, I. Tsaroom, S. Blum, J. J. Org. Ghent. 1978, 43,4271-4273. Jochanan Blum is a professor at The Hebrew University in Jemsalem, Israel. [Pg.61]

Richter, J. M. Blum aziridine synthesis. In Name Reactions in Heterocyclic Ghemistry 77 Li, J. J., Ed. Wiley Hoboken, NJ, 2011, pp 2-10. (Review). [Pg.61]

Name Reactions, 4th ed., DOI 10.1007/978-3-642-01053-8 25, Springer-Verlag Berlin Heidelberg 2009 [Pg.52]


See other pages where Blum-Ittah aziridine synthesis is mentioned: [Pg.60]    [Pg.52]    [Pg.60]    [Pg.52]   
See also in sourсe #XX -- [ Pg.52 ]

See also in sourсe #XX -- [ Pg.60 ]

See also in sourсe #XX -- [ Pg.52 ]




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