Stereochemistry of nucleophilic ring-opening reactions of optically active N-acetyl-2-methoxycarbonylaziridine
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference7 articles.
1. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations
2. Single electron transfer versus nucleophilic ring opening in reactions of cis-trans pairs of activated 2-phenylaziridines. Strong influence of nitrogen pyramid for N-benzoylaziridines
3. Synthesis of functionalized phenylalanine derivatives by ring opening reactions of 3-arylaziridine-2-carboxylic esters
4. Preparation of .beta.-substituted tryptophan derivatives: comparison of the reactivity of N-methylindole toward aziridine-2-lactones and aziridine-2-carboxylic esters and interpretation of results using MNDO calculations
5. OPTICAL ENANTIOMORPHS OF α,β-DIAMINOPROPIONIC ACID
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