Deprotection of Sulfonyl Aziridines
Author:
Affiliation:
1. Department of Organic Chemistry, Uppsala University, Box 531, S-751 21 Uppsala, Sweden
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9815296
Reference61 articles.
1. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations
2. (b) Kump, J. E. G.Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 7, p 469.
3. Efficient Syntheses of (1R,2R)- and (1S,2S)-2-Amino-1-alkyl(or aryl)-1,3-propanediols by Regioselective Ring Opening of Aziridine-2-methanols
4. A Highly Stereoselective Aza-[3,3]-Claisen Rearrangement of Vinylaziridines as a Novel Entry to Seven-Membered Lactams
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