A simple one-pot preparation of diazoacetoacetate derivatives from aldehydes.
Marvis O Erhunmwunse, Patrick G Steel
文献索引:J. Org. Chem. 73(21) , 8675-7, (2008)
全文:HTML全文
摘要
Diazoacetoacetate derivatives can be simply and efficiently prepared from aldehydes in a one-pot process involving initial DBU-promoted "aldol" condensation with ethyl diazoacetate followed by in situ oxidation with IBX. Aryl, alkyl, and unsaturated aldehydes are all viable substrates.
相关化合物
相关文献:
2001-10-05
[J. Org. Chem. 66(20) , 6729-33, (2001)]
Niobium (V) chloride-catalyzed C-H insertion reactions of a-diazoesters: synthesis of ß-keto esters. Yadav JS, et al.
[Tetrahedron 61(4) , 875-78, (2005)]
Reaction of dimethyl diazomalonate and ethyl 2-diazoacetoacetate with N-methylpyrrole. Maryanoff BE.
[J. Org. Chem. 47(15) , 3000-3002., (1982)]