ChemInform Abstract: Nucleophilic Ring Opening of Aziridines
โ Scribed by Helmut Stamm
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 24 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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๐ SIMILAR VOLUMES
Regioselective Nucleophilic Ring Opening of Epoxides and Aziridines Derived from Homoallylic Alcohols. -The title investigation is carried out with a view to providing a method for the regioselective preparation of 1,4diols or amino alcohols as building blocks for the synthesis of natural products.
Regioselective Nucleophilic Ring Opening Reactions of 2,2-Disubstituted Aziridines -The Asymmetric Synthesis of ฮฑ,ฮฑ-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
This account of research work on nucleophilic ring opening (NRO) of aziridines (Az's) demonstrates the broad synthetic scope of this reaction, inclusive secondary reactions, and it discusses the special mechanistic fundamentals and details as well as mechanistic variants. Formation of a C-C bond by