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Enolate compounds processes, lactone synthesis

As discussed in Chapter 9, various nucleophiles can be introduced at the ortho position of nitroarenes via the VNS process. This provides a useful strategy for the synthesis of indoles. One of the most attractive and general methods of indoles and indolinones would be the reductive cyclization of a-nitroaryl carbonyl compounds (Eq. 10.54). The VNS and related reactions afford a-nitroaryl carbonyl compounds by a simple procedure. For example, alkylation of 4-fluoronitrobenzene with a lactone silyl enol ether followed by reductive cyclization leads to tryptophols (Eq. 10.55).73... [Pg.341]


See other pages where Enolate compounds processes, lactone synthesis is mentioned: [Pg.712]    [Pg.712]    [Pg.296]    [Pg.341]    [Pg.296]    [Pg.296]    [Pg.137]    [Pg.296]    [Pg.185]    [Pg.98]    [Pg.301]    [Pg.16]    [Pg.1111]    [Pg.1708]    [Pg.1111]   


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8-lactone synthesis

Compound processing

Compounding process

Enol lactones

Enol synthesis

Enolate compound

Enolate compounds processes

Enolate synthesis

Enolates compounds

Lactone enolate

Lactones compounds

Lactones enolates

Lactones synthesis

Lactones, enolization

Process synthesis

Processing synthesis

Synthesis enolates

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