1999Unpublished venueOpen access

Synthesis of Heterocycles Using Tandem Cyclization Processes.

Albert Padwa

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Abstract

Various applications of the cycloaddition/N-acyliminium ion tandem cyclization cascade are outlined in this electronic symposium on synthetic organic chemistry. The key step in the process involves the generation of a reactive N-acyliminium ion by fragmentation of an amino substituted [4+2]-cycloadduct. The successful synthesis of a number of alkaloids by this sequence of reactions reveals the usefulness and importance of this unique domino cascade.

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What this paper is about

Various applications of the cycloaddition/N-acyliminium ion tandem cyclization cascade are outlined in this electronic symposium on synthetic organic chemistry. The key step in the process involves the generation of a reactive N-acyliminium ion by fragmentation of an amino substituted [4+2]-cycloadduct. The successful synthesis of a number of alkaloids by this sequence of reactions reveals the usefulness and importance of this unique domino cascade.

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Available abstract

Various applications of the cycloaddition/N-acyliminium ion tandem cyclization cascade are outlined in this electronic symposium on synthetic organic chemistry. The key step in the process involves the generation of a reactive N-acyliminium ion by fragmentation of an amino substituted [4+2]-cycloadduct. The successful synthesis of a number of alkaloids by this sequence of reactions reveals the usefulness and importance of this unique domino cascade.

Key concepts: Tandem, Cascade, Domino, Cycloaddition, Fragmentation (computing), Cascade reaction, Combinatorial chemistry, Computer science

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