Abstract
This article has no abstract. Keywords: aldol and michael reactions; allylation; friedel–crafts acylation; diels–alder reactions; acetalization; O-acylation; friedel–crafts reactions; decarbonylation; allylation; aldol reactions; γ-hydroxy ketones; α,β-unsaturated thioimidates; polymeric catalysts; allylation; aldol and mannich-type reactions; amines via condensations; protection of oxygen functions; carbonyl-ene reaction; friedel–crafts reactions; structural homolog; allylation; aldol reactions; mannich reactions; tishchenko reaction; cyclocondensation; friedel–crafts alkylation; hydrolysis; silyl ethers; functional group transformations; alkylation; nitration; diels-alder reaction; functional group transformations; substitutions; additions; hydroamination; ring cleavage; (z)-chloroalkenes; substitution; mannich reaction; michael reaction; α-hydroxyalkyl-γ-lactams; cycloaddition; cycloisomerization; transesterification; meyer–schuster rearrangement; addition reactions; annulation; friedel–crafts reactions; coupling; samarium(III) chloride; Negishi coupling; samarium(III) tris(hexamethyldisilazide); Wolff rearrangement; silver trifluoroacetate
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