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Diversomer libraries consisting of substituted cyclopentanes and cyclohexanes 3 were produced by Knoevenagel reaction of polymer-bound malonate 1 and aldehydes 2, subsequent ene reaction, and cleavage from the support. In this domino solid-phase procedure the simple and induced diastereoselectivities of the ene reaction are generally very satisfactory (>99:1). R = H, Me, nBu, Ph.
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Tietze et al. (1996) studied this question.
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