Dehydrocholic acid (DHCA), an unnatural bile acid, is manufactured by oxidation of cholic acid. Its biotransformation by two basidiomycetes (Trametes hirsuta and Collybia velutipes) is reported. These mycelia showed different affinities for the substrate and selectivities of attack: T. hirsuta in particular regio- and stereoselectively reduced the 3-keto group to yield 3-hydroxy-7,12-diketo-5-cholan-24-oic acid (7,12-diketolithocolic acid) as the main product. A number of different chemical reductions were carried out on DHCA; among them hydrogenation with Raney Nickel in water under high-intensity ultrasound proved highly regio- and stereoselective, yielding 7,12-diketolithocolic acid exclusively. 1H and 13C resonances were assigned in details thanks to a series of 1D and 2D NMR runs including DEPT, NOESY, H–H COSY, gHSQC and gHMBC.

Regio- and stereoselective reductions of dehydrocholic acid / G. CRAVOTTO; A. BINELLO; L. BOFFA; O. ROSATI; M. BOCCALINI; S. CHIMICHI. - In: STEROIDS. - ISSN 0039-128X. - STAMPA. - 71:(2006), pp. 469-475. [10.1016/j.steroids.2006.01.004]

Regio- and stereoselective reductions of dehydrocholic acid

BOCCALINI, MARCO;CHIMICHI, STEFANO
2006

Abstract

Dehydrocholic acid (DHCA), an unnatural bile acid, is manufactured by oxidation of cholic acid. Its biotransformation by two basidiomycetes (Trametes hirsuta and Collybia velutipes) is reported. These mycelia showed different affinities for the substrate and selectivities of attack: T. hirsuta in particular regio- and stereoselectively reduced the 3-keto group to yield 3-hydroxy-7,12-diketo-5-cholan-24-oic acid (7,12-diketolithocolic acid) as the main product. A number of different chemical reductions were carried out on DHCA; among them hydrogenation with Raney Nickel in water under high-intensity ultrasound proved highly regio- and stereoselective, yielding 7,12-diketolithocolic acid exclusively. 1H and 13C resonances were assigned in details thanks to a series of 1D and 2D NMR runs including DEPT, NOESY, H–H COSY, gHSQC and gHMBC.
2006
71
469
475
G. CRAVOTTO; A. BINELLO; L. BOFFA; O. ROSATI; M. BOCCALINI; S. CHIMICHI
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/203919
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