Studies in Spiroketal Synthesis 2. A Tandem Cyclization Route to the 1,7-Dioxaspiro[5.5]undecane Ring System

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Synlett | / 11卷 / 1065期

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[41] Structure of the 1 : 1 Complex of Hexakis(2,3,6-tri- O-methyl) α-Cyclodextrin with ( R)-(-)-1,7-Dioxaspiro[5.5]undecane
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[42] Chiral recognition of (R)-(-)-1,7-dioxaspiro[5.5]undecane by hexakis(2,3,6-tri-O-methyl)-alpha-cyclodextrin
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[43] PHEROMONES .53. SYNTHESIS OF (3S,6R)-3-HYDROXY-1,7-DIOXASPIRO [5.5]UNDECANE AND (3S,6S)-3-HYDROXY-1,7-DIOXASPIRO[5.5]UNDECANE - A COMPONENT OF OLIVE FLY PHEROMONE COMPLEX (DACUS-OLEAE)
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[45] Synthesis and herbicidal activity of [3R*,5S*,6S*]-3-benzyloxy-5-methoxy-1,7-dioxaspiro[5.5]undecane and [3R*,5S*,6S*]-3-methoxy-5-benzyloxy-1,7-dioxaspiro[5.5]undecane
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[46] [3S*,5S*,6S*]-1,7-dioxaspiro[5.5]undecane-3,5-diol
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[50] SYNTHESIS OF 2,8-SUBSTITUTED 1,7-DIOXASPIRO[5.5]UNDECANES AND 1,4,7,10-TETRAOXASPIRO[5.5]UNDECANES BY AN OXYAMINATION REACTION
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