α,β-Unsaturated oxime as a new heterodiene for the diels alder reaction synthesis of furo [2,3-c] pyridine n-oxides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. 1-AZA-1,3-dienes. Diels-alder reactions with α, β-unsaturated hydrazones.
2. A Convenient Synthesis of Alkyl 2-Alkoxycarbonyl-3-pyridineacetates
3. XY–ZH systems as potential 1,3-dipoles. Part 2. Oxime cycloadditions: formation of 2 : 1 adducts
4. Furopyridines. I. Synthesis of furo[2,3-c]pyridine
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1. ChemInform Abstract: α,β-Unsaturated Oxime (I) as a New Heterodiene for the Diels-Alder Reaction. Synthesis of Furo(2,3-c)pyridine N-Oxides (IV), ( VII).;ChemInform;2010-08-22
2. Synthesis of Heterocycles from Oximes;PATAI'S Chemistry of Functional Groups;2010-04-15
3. Rh(I)-catalyzed intramolecular hetero-[4+2] cycloaddition of ω-alkynyl-vinyl oximes;Tetrahedron Letters;2007-09
4. Interesting Behavior of α,β-Unsaturated Oximes in Intramolecular [4 + 2] Cycloaddition Reactions;Organic Letters;2004-05-15
5. STUDY OF THE REACTIONS OF FOUR INDOLIC 1-AZADIENES WITH A FEW ENOIC, YNOIC, AND AZO DIENOPHILES;Synthetic Communications;2002-01
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