Regioselective Nucleophilic Ring Opening Reactions of 2,2-Disubstituted Aziridines -The Asymmetric Synthesis of α,α-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
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ChemInform Abstract: Chemo- and Regioselective Nucleophilic Reactions of (Bromomethyl)methylmaleic Anhydride: Synthesis of α-Quinoxalinyl- and α-Benzothiazinylacrylic Acids.
✍ Scribed by Anil M. Deshpande; Arvind A. Natu; Narshinha P. Argade
- Book ID
- 101889520
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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