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The Reaction of β-Amino Alcohols with 1,1′-Carbonyldiimidazole − Influence of the Nitrogen Substituent on the Reaction Course

✍ Scribed by Sara Cutugno; Gianluca Martelli; Lucia Negro; Diego Savoia

Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
342 KB
Volume
2001
Category
Article
ISSN
1434-193X

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✦ Synopsis

The reaction of β-amino alcohols with 1,1Ј-carbonyldiimidazole in dichloromethane is affected by the size of the nitrogen substituent. 1,3-Oxazolidin-2-ones are exclusively obtained from N-H, N-methyl and N-arylmethyl derivatives. O-(1-Imidazolyl)carbonyl derivatives are formed as intermediates [a

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ChemInform Abstract: The Reaction of β-A
ChemInform Abstract: The Reaction of β-Amino Alcohols with 1,1′-Carbonyldiimidazole — Influence of the Nitrogen Substituent on the Reaction Course.
✍ Sara Cutugno; Gianluca Martelli; Lucia Negro; Diego Savoia 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB

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