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Diastereoselectivity cyclic allyl alcohol derivatives

CHMO.. has been used in the diastereoselective oxidation of different p-hydroxy sulfides to the corresponding chiral p-hydroxy sulfoxides. Chiral p-hydroxy sulfoxides represent interesting compounds used as chiral auxiliaries in asymmetric synthesis, asymmetric ligands, or as building blocks for the synthesis of cyclic sulfides, benzoxathiepines, allylic alcohols, or leukotrienes [27]. The sulfoxidation of these substrates is a kinetic resolution, in which both the sulfide and the sulfoxide can be obtained in chiral form. Oxidation of the cyclohexyl derivative (Table 6.1, entry 2) by a semipurified preparation of in the presence of the enzymatic... [Pg.152]


See other pages where Diastereoselectivity cyclic allyl alcohol derivatives is mentioned: [Pg.410]    [Pg.903]    [Pg.410]    [Pg.731]    [Pg.101]    [Pg.212]    [Pg.38]    [Pg.1173]    [Pg.1173]    [Pg.109]    [Pg.180]    [Pg.180]    [Pg.280]    [Pg.180]    [Pg.974]    [Pg.93]    [Pg.38]    [Pg.43]    [Pg.1006]    [Pg.149]    [Pg.36]    [Pg.175]   
See also in sourсe #XX -- [ Pg.836 , Pg.837 ]




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3- allyl alcohol derivatives

5-Allyl-derivatives

Alcohols derivatives

Alcohols, cyclic

Allyl alcohols diastereoselectivity

Allylic alcohols cyclic derivatives

Allylic alcohols diastereoselective

Allylic alcohols diastereoselectivity

Allylic derivatives

Allylic derivatives cyclic allylation

Allylic derivatives diastereoselectivity

Allylic diastereoselective

Cyclic allylic alcohol

Cyclic derivatives

Diastereoselective allylations

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