Synthetic strategy toward skeletal diversity via solid-supported, otherwise unstable reactive intermediates

Angewandte Chemie - International Edition

Volumn 43, Issue 13, 2004, Pages 1681-1685

  Taylor, Steven J ^a   Taylor, Alexander M ^a   Schreiber, Stuart L ^a  

^a HARVARD UNIVERSITY   (United States)

Author keywords

Diversity oriented synthesis; Enamines; Nitrogen heterocycles; Reactive intermediates; Solid phase synthesis

Indexed keywords

ALKYLATION; MATHEMATICAL TRANSFORMATIONS; REDUCTION; STABILITY; SYNTHESIS (CHEMICAL);

CYCLOADDITIONS; MACROBEADS; SKELETAL DIVERSITY;

CHEMICAL BONDS;

ALKALOID; DIHYDROISOQUINOLINE; DIHYDROPYRIDINE; ENAMINE; ISOQUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CHEMICAL BOND; CHEMICAL REACTION; CYCLOADDITION; MATERIALS; REDUCTION; SOLID; SYNTHESIS;

ALKALOIDS; AMINES; DIHYDROPYRIDINES; ISOQUINOLINES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; REFERENCE STANDARDS;

EID: 4544326369     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200353466     Document Type: Article

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