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Vanadyl-catalyzed epoxidation

Vanadyl Acetyloacctonate Catalyzed Epoxidation of 4-CycloIiexyl-4-hydroxy-3-methylene-2-butanone Typical Procedure31 ... [Pg.161]

With compound 64 available, vanadyl acetylacetonate catalyzed epoxidation [44] accompanied by simultaneous cyclization, afforded the corresponding tetrahydrofuran and its diastereomer in a 4 1 ratio (Scheme 12). Ring expansion of the corresponding mesylate 65 with silver (I) carbonate afforded compound 66 in a 42% yield for the two steps [45]. Extension of the side chain in six steps, followed by an asymmetric epoxidation, gave product 67 stereoselectively. The cyclization of 67 with titanium tetraisopropoxide in a manner consistent with model studies [27d], afforded bicyclic ether 68 in 65% yield. Transformation to the epoxide under standard conditions afforded fragment 69 ready to be coupled with the D-ring side chain. [Pg.26]


See other pages where Vanadyl-catalyzed epoxidation is mentioned: [Pg.124]    [Pg.827]    [Pg.183]    [Pg.29]    [Pg.7]    [Pg.532]    [Pg.95]    [Pg.95]    [Pg.185]    [Pg.469]    [Pg.462]    [Pg.95]    [Pg.2134]   
See also in sourсe #XX -- [ Pg.1130 , Pg.1131 ]




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Epoxides catalyzed

Vanadyl

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