Regioselective Nucleophilic Ring Opening Reactions of 2,2-Disubstituted Aziridines -The Asymmetric Synthesis of Ξ±,Ξ±-Disubstituted Amino Acids. -It is shown that, under appropriate conditions, 2,2disubstituted aziridines like (I) and (V) undergo regioselective ring opening reactions at C-3 with carb
β¦ LIBER β¦
Synthesis ofgem-disubstituted taurines by the regioselective ring-opening of 2,2-disubstituted aziridines with sodium bisulfite and sulfite
β Scribed by Ning Chen; Min Zhu; Wei Zhang; Da-Ming Du; Jiaxi Xu
- Book ID
- 106221709
- Publisher
- Springer
- Year
- 2008
- Tongue
- English
- Weight
- 383 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0939-4451
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