Amidation through carbamates
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Other documents of the author: Latorre, Antonio; Rodríguez, Santiago; Izquierdo Ferrer, Javier; González, Florenci
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comunitat-uji-handle2:10234/7053
comunitat-uji-handle3:10234/8639
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http://dx.doi.org/10.1016/j.tetlet.2009.03.113 |
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Title
Amidation through carbamatesDate
2009Publisher
ElsevierISSN
404039Bibliographic citation
Tetrahedron Letters, 50, 22, p. 2653-2655Type
info:eu-repo/semantics/articleSubject
Abstract
N-Alkyl carbamates of primary amines are easily converted into amides under treatment with Grignard reagents. Consequently, primary amines can be converted into amides in a one-pot reaction through carbamate protection ... [+]
N-Alkyl carbamates of primary amines are easily converted into amides under treatment with Grignard reagents. Consequently, primary amines can be converted into amides in a one-pot reaction through carbamate protection and Grignard addition. © 2009 Elsevier Ltd. All rights reserved. [-]
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info:eu-repo/semantics/restrictedAccess
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- QUIO_Articles [689]