Four mechanisms in the reactions of 3-aminopyrrole with 1,3,5-triazines: Inverse electron demand diels-alder cycloadditions vs SNAr reactions via uncatalyzed and acid-catalyzed pathways

Journal of Organic Chemistry

Volumn 78, Issue 17, 2013, Pages 8614-8623

  De Rosa, Michael ^a   Arnold, David ^a   Hartline, Douglas ^a  

^a PENNSYLVANIA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACID-CATALYZED PATHWAYS; DIELS-ALDER CYCLOADDITIONS; DOUBLE SUBSTITUTION; HETEROCYCLIC RINGS; INVERSE-ELECTRON DEMAND DIELS-ALDER REACTIONS; ONE-STEP REACTIONS; PYRIMIDINE DERIVATIVES; TWO-STEP REACTIONS;

CARBON DIOXIDE; CATALYSIS;

CYCLOADDITION;

3 AMINOPYRROLE; ACID; AMINE; HETEROCYCLIC COMPOUND; PYRIMIDINE DERIVATIVE; PYRROLE DERIVATIVE; TETRAPHENYLBORON; TRIAZINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CYCLOADDITION; DIELS ALDER REACTION; QUANTUM YIELD; REACTION ANALYSIS; SUBSTITUTION REACTION; X RAY CRYSTALLOGRAPHY;

ACIDS; CATALYSIS; CYCLIZATION; ELECTRONS; MOLECULAR STRUCTURE; PYRROLES; TRIAZINES;

EID: 84883781035     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo4012915     Document Type: Article

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