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Bardhan-Sengupta synthesis

BARDHAN-SENGUPTA SYNTHESIS. Phosphorus pentoxide and other powerful dehydrating agents act upon 2-beta-phenethyl-l-cyclohexanol to form oclahydrophenanlhrene compounds. [Pg.171]

Other refereces related to the Bardhan-Sengupta synthesis are cited in the literature. ... [Pg.218]

This reaction is related to the Bardhan Sengupta Synthesis. [Pg.457]

Much like the work conducted by the Bogert and Cook groups, the Bardhan-Sengupta synthesis of phenanthrenes helped lead to the determination of the carbon framework for steroids and was used to prepare terpene-type natural products. [Pg.199]

The Bardhan-Sengupta Phenanthrene Synthesis uses P2Os in place of H2SO . [Pg.524]

Another Friedel-Crafts route to phenanthrenes is the Bardhan-Sengupta phenanthrene synthesis. When phenethylcyclohexanol 222 was cyclized with phosphorus pentoxide at 140°C, the product was 223. Aromatization was accomplished by heating with selenium to give the phenanthrene derivative 224 (1-methyl-7-isopropylphenanthrene, otherwise known as retene). An improvement in the reaction used hydrogen fluoride (HF) to induce cyclization.l ... [Pg.1095]


See other pages where Bardhan-Sengupta synthesis is mentioned: [Pg.996]    [Pg.996]    [Pg.215]    [Pg.215]    [Pg.216]    [Pg.218]    [Pg.996]    [Pg.996]    [Pg.215]    [Pg.215]    [Pg.216]    [Pg.218]    [Pg.121]    [Pg.661]    [Pg.197]    [Pg.198]    [Pg.198]    [Pg.762]    [Pg.27]   
See also in sourсe #XX -- [ Pg.996 ]

See also in sourсe #XX -- [ Pg.996 ]




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Bardhan-Sengupta phenanthrene synthesis

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