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Benz isoquinolines synthesis

Benz[g]isoquinoline, l,4-ethano-l,2,3,4-tetrahydro-nomenclature, 1, 20 Benz[g]isoquinolinequinone synthesis... [Pg.539]

Increasingly, this process has been adapted to the synthesis of heterocyclic systems. One or both of the phenyl substituents in stilbene can be replaced by a heteroaromatic system, and some of the more important of these cyclizations are recorded in Table I. The formation of benz[A]isoquinoline by photolysis of 4-styrylpyridine in cyclohexane is accompanied by the formation of 1- and 3-cyclo-hexylbenz[A]isoquinoline.346... [Pg.88]

Cervinomycins (126 and 127) have captured interest as synthetic targets for organic synthesis. So far two approaches [104, 105] for the synthesis of partial structures and one total synthesis [106] of cervinomycin have been reported. At the outset, the rationale of the synthetic tactics towards these molecules was to secure an appropriate methodology for constructing the oxazolo-[3,2]-benz(o)isoquinoline skeleton. We envisioned that this moiety might be prepared in a single step from the corresponding isocoumarin (137) and ethanolamine. [Pg.521]


See other pages where Benz isoquinolines synthesis is mentioned: [Pg.539]    [Pg.539]    [Pg.539]    [Pg.539]    [Pg.539]    [Pg.539]    [Pg.167]    [Pg.411]    [Pg.259]    [Pg.34]    [Pg.97]    [Pg.411]    [Pg.178]    [Pg.16]    [Pg.95]   
See also in sourсe #XX -- [ Pg.52 , Pg.220 , Pg.279 ]




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