Reaction of benzyloxycarbonyl-5-oxazolidinones and of N-benzyloxycarbonylamino acids with BCl3 in dichloromethane at room temperature affords the corresponding free amino acids.
Facile and rapid regeneration of free amino acids from N-benzyloxycarbonyl-5-oxazolidinones and from N-benzyloxycarbonylamino derivatives by treatment with BCl3 in dichloromethane / P. Allevi, R. Cribiù, M. Anastasia. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 45:30(2004 Jul 19), pp. 5841-5843. [10.1016/j.tetlet.2004.06.011]
Facile and rapid regeneration of free amino acids from N-benzyloxycarbonyl-5-oxazolidinones and from N-benzyloxycarbonylamino derivatives by treatment with BCl3 in dichloromethane
P. AlleviPrimo
;R. CribiùSecondo
;M. AnastasiaUltimo
2004
Abstract
Reaction of benzyloxycarbonyl-5-oxazolidinones and of N-benzyloxycarbonylamino acids with BCl3 in dichloromethane at room temperature affords the corresponding free amino acids.
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