Production Method 1

145-13-1

82538-36-1

600-72-6

95832-17-0

595-59-5

80-75-1

Reaction Conditions

1.1 Reagents: Glucose Solvents: Acetone ,  Water ;  3 d, 25 °C

Reference

Novel metabolites of dehydroepiandrosterone and progesterone obtained in Didymosphaeria igniaria KCH 6670 culture

Janeczko, Tomasz; et al, Journal of Molecular Catalysis B: Enzymatic, 2012, 82, 24-31

Production Method 2

57-83-0

82538-36-1

27534-93-6

600-72-6

95832-17-0

601-90-1

595-59-5

80-75-1

Reaction Conditions

1.1 Reagents: Glucose Solvents: Acetone ,  Water ;  3 d, 25 °C

Reference

Novel metabolites of dehydroepiandrosterone and progesterone obtained in Didymosphaeria igniaria KCH 6670 culture

Janeczko, Tomasz; et al, Journal of Molecular Catalysis B: Enzymatic, 2012, 82, 24-31

Pregn-4-ene-3,20-dione, 11,15-dihydroxy-, (11a,15b)- Raw materials

• Progesterone
• Pregnenolone

Pregn-4-ene-3,20-dione, 11,15-dihydroxy-, (11a,15b)- Preparation Products

• Pregn-4-ene-3,20-dione,7-hydroxy-, (7a)-(9CI) (27534-93-6)
• 15β-Hydroxy Progesterone (600-72-6)
• Pregn-4-ene-3,20-dione,11,14-dihydroxy-, (11a)- (9CI) (95832-17-0)
• Pregn-4-ene-3,20-dione, 11,15-dihydroxy-, (11a,15b)- (82538-36-1)
• (7beta,15beta)-7,15-Dihydroxypregn-4-ene-3,20-dione (601-90-1)
• Pregn-4-ene-3,20-dione, 14,15-dihydroxy-, (15b)- (595-59-5)
• 11a-Hydroxy Progesterone (80-75-1)

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