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Of -steganacin

Mont N, Mehta VP, Appukkuttan P et al (2008) Diversity oriented microwave-assisted synthesis of (-) -Steganacin aza-analogues. J Org Chem 73 7509-7516... [Pg.230]

SCHEME 125. Biomimetic synthesis of steganacin and related compounds... [Pg.1281]

Hernandin (15) is a new compound which belongs to the category of phenyl-tetralin-type lignans. Many studies have been reported on the syntheses of this type lignans (ref. 2, 47), and some of them were carried out in connection with the syntheses of steganacin (ref. 48) and deoxyschizandrin (ref. 49). A route via an itaconic acid derivative, obtained by Stobbe condensation of a benzophenone derivative with diethyl succinate, followed by cyclization (ref. 41a, 50) was first undertaken through the scheme outlined in Chart 10. [Pg.579]

Optically pure l-(3, 4 -methylenedioxyphenyl)ethanol is a key chiral intermediate for the synthesis of Steganacin and Salmeterol. Apara-nitrobenzyl esterase cloned from Bacillus amyloliquefaciens (BAE) was employed to hydrolyze... [Pg.33]

See other pages where Of -steganacin is mentioned: [Pg.356]    [Pg.385]    [Pg.386]    [Pg.388]    [Pg.392]    [Pg.393]    [Pg.401]    [Pg.1278]    [Pg.1300]    [Pg.356]    [Pg.385]    [Pg.386]    [Pg.388]    [Pg.392]    [Pg.401]    [Pg.216]    [Pg.88]    [Pg.190]    [Pg.510]   
See also in sourсe #XX -- [ Pg.24 , Pg.779 ]



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Stegane synthesis of -steganacin

Steganes synthesis of -steganacin

Synthesis of -steganacin

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