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Enantioselective Synthesis and Stereoselective Ring Opening of N-Acylaziridines

✍ Scribed by Jennifer Cockrell; Christopher Wilhelmsen; Heather Rubin; Allen Martin; Prof. Jeremy B. Morgan


Book ID
115549703
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
574 KB
Volume
124
Category
Article
ISSN
0044-8249

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The neutral hydrolysis of N-acyl-2,2-dimethylaziridines gave rise to the amidoalcohols in 76-91% overall yields. These products resulted from the specific cleavage of the C-2-N bond.