Synthesis of chiral 1,2-diols and relate
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Yukio Masaki; Yuzuru Serizawa; Kinnosuke Nagata; Hirohisa Oda; Hiromu Nagashima;
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Article
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1986
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Elsevier Science
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French
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octanes, prepared from (+)-tartaric acid, were converted by means of an organoaluminium reagent Et2AlSPh into the pyranoid monothioacetals, which were utilized via the successive thioacetalization to the synthesis of the insect pheromones (+)-disparlure and (-)-(2S,3S)-octanediol.