Synthesis of acetyl-substituted heterocyclic enamines and their reaction with diethyl azodicarboxylate

Article abstract of DOI:10.1080/00397919508013835

Acetyl-substituted heterocyclic enamines 4 were synthesized from lactim ethers 2 and acetylacetone through condensation and deacetylation reactions, and they, along with the ester-substituted heterocyclic enamines 6, reacted with diethyl azodicarboxylate to afford C-adducts 7 and 8 in excellent yields.

Full text of DOI:10.1080/00397919508013835

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Synthesis of Acetyl-Substituted
Heterocyclic Enamines and
Their Reaction with Diethyl
Azodicarboxylate
Ying Cheng a , Min Zhao a , Mei-Xiang Wang b , Li-Ben
Wang b & Zhi-Tang Huang b
a Department of Chemistry , Beijing Normal
University , Beijing, 100875, China
b Institute of Chemistry, Academia Sinica , Beijing,
100080, China
Published online: 23 Sep 2006.
To cite this article: Ying Cheng , Min Zhao , Mei-Xiang Wang , Li-Ben Wang & Zhi-
Tang Huang (1995) Synthesis of Acetyl-Substituted Heterocyclic Enamines and Their
Reaction with Diethyl Azodicarboxylate, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 25:9, 1339-1351,
DOI: 10.1080/00397919508013835
To link to this article: http://dx.doi.org/10.1080/00397919508013835
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