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Methyl hexanoate, reduction

So far, most microorganisms and enzymes derived therefrom have been used in the reduction of a single keto group of p-keto or a-keto compounds [68-71], Recently, Patel et al. [72] have demonstrated the stereoselective reduction of 3,5-dioxo-6-(benzyloxy)hexanoic acid, ethyl ester (41), to (3,S, 5R)-dihydroxy-6-(benzyloxy)hexanoic acid, ethyl ester (42a) (Fig. 14). The compound (42a) is a key chiral intermediate required for the chemical synthesis of [4-[4a,6P(E)]]-6-[4,4-bis(4-fluorophenyl)-3-(l-methyl-lH-tetrazol-5-yl)-l,3-butadienyl]-tetrahydro-4-hydroxy-2H-pyran-2-one, compound R-( + )-(43), a new anticholesterol drug that acts by inhibition of HMG CoA reductase [73], Among various microbial cultures evaluated for the stereoselective reduction of diketone (41), cell suspensions of Aci-... [Pg.157]


See other pages where Methyl hexanoate, reduction is mentioned: [Pg.148]    [Pg.2]    [Pg.388]    [Pg.1514]    [Pg.235]    [Pg.235]    [Pg.76]    [Pg.212]    [Pg.100]   
See also in sourсe #XX -- [ Pg.149 ]




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1-Hexano

Hexanoate

Hexanoic

Methyl reductions

Reductive methylation

Reductive methylations

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