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Synthesis 2005(1): 158-160
DOI: 10.1055/s-2004-831218
DOI: 10.1055/s-2004-831218
PSP
© Georg Thieme Verlag Stuttgart · New York
Facile Preparation of tert-Butyl 1-tert-Butoxycarbonylaminocyclopent-3-enecarboxylate from Inexpensive Starting Materials
Further Information
Publication History
Received
30 March 2004
Publication Date:
16 September 2004 (online)


Abstract
1,5-C,C-Cycloalkylation of tert-butyl acetoacetate (1) with cis-1,4-dichloro-2-butene (2) followed by the haloform reaction of the product in NaOH solution and subsequent Curtius degradation in tert-butyl alcohol furnished tert-butyl 1-tert-butoxycarbonylaminocyclopent-3-enecarboxylate (5) in 32% overall yield.
Key words
alkenes - cyclizations - excitatory amino acids - haloform reaction - Curtius rearrangement