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HRID597440

反应详情

EQUATION

反应方程式

HRID 597440 的结构方程式

REACTANTS

反应物

8
结构：C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
HCID5881

Dehydroepiandrosterone

C19H28O2

结构：CC(=O)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
HCID5994

Progesterone

C21H30O2

结构：CC(=O)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
HCID8955

Pregnenolone

C21H32O2

结构：C[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O)CC[C@@]43C)[C@@H]1CC[C@@H]2O
HCID10634

Androstenediol

C19H30O2

结构：C[C@]12CCC(=O)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
HCID222865

Dihydroandrostendione

C19H28O2

结构：C[C@]12CC[C@H](O)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)CC[C@@H]12
HCID242332

3beta,17beta-Androstanediol

C19H32O2

结构：C[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O)CC[C@@H]43)[C@@H]1CC[C@@H]2O
HCID9900246

19-Nor-5-androstenediol

C18H28O2

结构：C[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O)CC[C@@H]43)[C@@H]1CCC2=O
HCID53990402

19-Nordehydroepiandrosterone

C18H26O2

PRODUCTS

生成物

1
结构：C[C@]12C[C@H](O)[C@@H]3c4ccc(O)cc4CC[C@H]3[C@@H]1CC[C@@H]2O
HCID227673

CHEBI:62848

C18H24O3

PROCEDURE

实验过程

This reduction procedure is useful for the preparation of the 11α-acid succinates of 11α-hydroxy analogs of dehydroepiandrosterone, pregnenolone, progesterone, 3β-hydroxy-estr-5-en-17-one, and 5α-androstane-3,17-dione to 11α-hydroxy succinate derivatives of androst-5-ene-3β,17β-diol, pregn-5-ene-3β,20α and 20β diols, pregn-4-ene-3,20α and 20β diols, estr-5-en-3β,17β-diol and 5α-androstane-3β,17β-diol.