2-oxo-3-butenoate esters as dienophiles and their utility in a novel synthesis of pyrroles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Accelerated inverse electron demand Diels-Alder reactions of 1-oxa-1,3-butadienes: [4 + 2] cycloaddition reactions of .beta.,.gamma.-unsaturated .alpha.-keto esters
2. Divergent de novo synthesis of carbohydrates based on an accelerated inverse electron demand Diels-Alder reaction of 1-oxa-1,3-butadienes
3. Room-temperature, endo-specific 1-aza-1,3-butadiene Diels-Alder reactions: acceleration of the LUMOdiene-controlled [4 + 2] cycloaddition reactions through noncomplementary aza diene substitution
4. Hetero-Diels-Alder Reaction of Substituted 1-Oxabutadienes and 2-Ethoxyvinylacetate An entry to various natural occurring carbohydrates
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1. Arylidene pyruvic acids (APAs) in the synthesis of organic compounds;Tetrahedron;2012-08
2. ChemInform Abstract: 2-Oxo-3-butenoate Esters as Dienophiles and Their Utility in a Novel Synthesis of Pyrroles.;ChemInform;2010-08-22
3. Steric Effects of Silyl Groups;PATAI'S Chemistry of Functional Groups;2009-12-15
4. Synthetic Studies in Phytochrome Chemistry;Synlett;2005-10-27
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