3-(tributylstannyl)allyl alcohols: Useful building blocks for solid-phase synthesis of skipped dienes and trienes

Repeated Stille coupling of 3-substituted 3-(tributylstannyl)allyl alcohols 2 on a solid support was used to synthesize a 21 x 21 library of skipped d ienes and a 21 x 21 x 21 library of skipped trienes. Starting 3-(tributylst annyl)allyl alcohols were prepared by Pd-catalyzed hydrostannation of subst ituted prop-2-yn-1-ols, by hydroalumination by LiAlH4 followed with transme tallation to tin using tributyltin methoxide, or by substitution of chlorin e in (Z)-6-chloro-3-(tributylstannyl)hex-2-en-1-ol with appropriate nucleop hile. Synthesized libraries were tested for the activity to endorphin recep tors, but with negative results.