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Total Synthesis of Lignans and Polymeric Resveratrol by Friedel-Crafts Reactions

SCHEME 10.36 Short total synthesis of podophyllotoxin enabled by a Pd-catalyzed C(sp )—H arylation. [Pg.357]

5 TOTAL SYNTHESIS OF LIGNANS AND POLYMERIC RESVERATROL BY FRIEDEL-CRAFTS REACTIONS [Pg.357]

Cyclogalgravin (191) then can be served as a common intermediate for collective synthesis of stereodivergent aryltetralins and aryltetralones [(33, 194-199)] with anti-anti or (anti-)syn-anti arrangement of substituents in tetrahydronaphthalene (THN) skeleton through a series of redox reactions. In particular, the first racemic syntheses of [Pg.357]

SCHEME 1037 Synthetic tactic of 2,7 -cyclolignan class and their correlation. [Pg.358]

SCHEME 10.38 Total synthesis of galbulin and isogalbulin via cyclogalgravin and kadangnstin J. [Pg.359]




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By Total Synthesis

Friedel and Crafts Reaction

Friedel and Crafts synthesis

Friedel synthesis

Friedel-Crafts polymerization

Friedel-Crafts synthesis

Lignan

Lignans

Lignans synthesis

Of lignans

Of resveratrol

Polymeric synthesis

Polymerization reaction

Polymerization reactions and

Reaction total

Resveratrol

Resveratrole

Resveratrols

Synthesis Friedel-Crafts reactions

Synthesis and Reactions

Synthesis polymerization

Synthesis resveratrol

Total Synthesis of

Total lignans

Total synthesis reactions

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