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Estrogen sulfamates: a new approach to oral estrogen therapy

Reproduction fertility and development, 2001, Vol.13 (4), p.297

2001

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Sulfamates of various estrogens are prodrugs with increased systemic and reduced hepatic estrogenicity at oral application

The Journal of steroid biochemistry and molecular biology, 1995-12, Vol.55 (3), p.395-403

1995

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Novel oestrogen sulfamates: a new approach to oral hormone therapy

Expert opinion on investigational drugs, 1998-04, Vol.7 (4), p.575-589

1998

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Synthesis and conformation of four 16,17-diols in the 3-methoxy-13alpha-estra-1,3,5(10)-triene series

Steroids, 2003-02, Vol.68 (2), p.113-123

2003

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Effects of estradiol and estradiol sulfamate on the liver of ovariectomized or ovariectomized and hypophysectomized rats

The Journal of steroid biochemistry and molecular biology, 2002-04, Vol.80 (4), p.457-467

2002

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Effects of estradiol and estradiol sulfamate on the uterus of ovariectomized or ovariectomized and hypophysectomized rats

The Journal of steroid biochemistry and molecular biology, 2000-10, Vol.74 (3), p.99-107

2000

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The steroid story of Jenapharm: From the late 1940s to the early 1970s

Steroids, 1999-07, Vol.64 (7), p.439-445

1999

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Scavestrogen sulfamates: correlation between estrone sulfatase inhibiting and antioxidant effects

Canadian journal of physiology and pharmacology, 1998-02, Vol.76 (2), p.99

1998

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Synthesis of estrogen sulfamates: Compounds with a novel endocrinological profile

Steroids, 1996-12, Vol.61 (12), p.710-717

1996

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Influence of subchronic administration of oestradiol, ethinyloestradiol and oestradiol sulphamate on bile flow, bile acid excretion, and liver and biliary glutathione status in rats

Archives of toxicology, 1997-05, Vol.71 (7), p.443-449

1997

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Comparative toxicology of ethinylestradiol (EE) and a new estrogen without 17-alpha ethinyl group: 17-beta-estradiol-3-sulfamate (J 995)

Toxicology letters, 1996-10, Vol.88, p.100-100

1996

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The remarkable influence of steroid A/B-ring junction on the Wittig olefination reaction of the 11-oxo group : Towards the synthesis of 5α- and 5β-oriented Δ3-isomers of desogestrel

Steroids, 1998, Vol.63 (1), p.21-27

1998

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The remarkable influence of steroid A/B-ring junction on the Wittig olefination reaction of the 11-oxo group: Towards the synthesis of 5α- and 5β-oriented Δ 3-isomers of desogestrel

Steroids, 1998, Vol.63 (1), p.21-27

1998

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17β-Hydroxy-11α-(3′-sulfanylpropyl)oxy-estra-1,3,5(10)-trien-3-yl sulfamate – a novel hapten structure: toward the development of a specific enzyme immunoassay (EIA) for estra-1,3,5(10)-triene-3-yl sulfamates

Steroids, 1999, Vol.64 (7), p.460-471

1999

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Novel “scavestrogens” and their radical scavenging effects, iron-chelating, and total antioxidative activities: Δ8,9-dehydro derivatives of 17α-estradiol and 17β-estradiol

Steroids, 1997-03, Vol.62 (3), p.304-310

1997

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Novel estrogens and their radical scavenging effects, iron-chelating, and total antioxidative activities: 17α-substituted analogs of Δ9(11)-dehydro-17 β-estradiol

Steroids, 1997-11, Vol.62 (11), p.688-694

1997

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Ionic hydrogenation of 3-methoxy-14α,15α-methylenestra-1,3,5(10),8-tetraen-17α-ol: A correction

Steroids, 1996, Vol.61 (2), p.48-49

1996

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Synthesis of 13-ethyl-11-methylene-18,19-dinor-17α-pregn-4-en-20-yn-17-ol (desogestrel) and its main metabolite 3-oxo desogestrel

Tetrahedron, 1994, Vol.50 (36), p.10709-10720

1994

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Synthesis of (1S,4R)-(-)-4-Hydroxy-2-cyclopentenyl Acetate by a Highly Enantioselective Enzyme-Catalyzed Transesterification in Organic Solvents

Synthesis (Stuttgart), 1988, Vol.1988 (7), p.540-541

1988

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2,2-disubstituierte cyclopentan-1,3-dione—2

Tetrahedron, 1982-01, Vol.38 (9), p.1279-1283

1982

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2,2-disubstituierte cyclopentan-1,3-dione—2: Untersuchung der regioselektivität von alkylierungs-reaktionen an 2-methyl-cyclopentan-1,3-dion

Tetrahedron, 1982, Vol.38 (9), p.1279-1283

1982

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Steroide. XII [1]. Steroid-alkansulfonate

Journal für Praktische Chemie, 1970, Vol.312 (4), p.720-727

1970

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Sterode. VIII. Darstellung Racemischer und enantiomerer 19-Norsteroide

Journal für Praktische Chemie, 1969, Vol.311 (4), p.671-676

1969

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Syntheses and Reactions of 2,2-Disubstituted Cyclopentane-1,3-diones, 6. Conversion of 2-Methylcyclopentane-1,3-dione into 5-Methylcycloheptane-1,4-dione via 3-(1-Methyl-2,5-dioxocyclopentyl)propanal

Liebigs Annalen der Chemie, 1992-05, Vol.1992 (5), p.419-422

1992

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Die Bestimmung der Optischen Reinheit an Zwischenprodukten der Prostaglandinsynthese mit Hilfe der NMR-Spektroskopie

Journal für Praktische Chemie, 1983, Vol.325 (2), p.345-349

1983

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Estrogen sulfamates: a new approach to oral estrogen therapy

Sulfamates of various estrogens are prodrugs with increased systemic and reduced hepatic estrogenicity at oral application

Novel oestrogen sulfamates: a new approach to oral hormone therapy

Synthesis and conformation of four 16,17-diols in the 3-methoxy-13alpha-estra-1,3,5(10)-triene series

Effects of estradiol and estradiol sulfamate on the liver of ovariectomized or ovariectomized and hypophysectomized rats

Effects of estradiol and estradiol sulfamate on the uterus of ovariectomized or ovariectomized and hypophysectomized rats

The steroid story of Jenapharm: From the late 1940s to the early 1970s

Scavestrogen sulfamates: correlation between estrone sulfatase inhibiting and antioxidant effects

Synthesis of estrogen sulfamates: Compounds with a novel endocrinological profile

Influence of subchronic administration of oestradiol, ethinyloestradiol and oestradiol sulphamate on bile flow, bile acid excretion, and liver and biliary glutathione status in rats

Comparative toxicology of ethinylestradiol (EE) and a new estrogen without 17-alpha ethinyl group: 17-beta-estradiol-3-sulfamate (J 995)

The remarkable influence of steroid A/B-ring junction on the Wittig olefination reaction of the 11-oxo group : Towards the synthesis of 5α- and 5β-oriented Δ3-isomers of desogestrel

The remarkable influence of steroid A/B-ring junction on the Wittig olefination reaction of the 11-oxo group: Towards the synthesis of 5α- and 5β-oriented Δ 3-isomers of desogestrel

17β-Hydroxy-11α-(3′-sulfanylpropyl)oxy-estra-1,3,5(10)-trien-3-yl sulfamate – a novel hapten structure: toward the development of a specific enzyme immunoassay (EIA) for estra-1,3,5(10)-triene-3-yl sulfamates

Novel “scavestrogens” and their radical scavenging effects, iron-chelating, and total antioxidative activities: Δ8,9-dehydro derivatives of 17α-estradiol and 17β-estradiol

Novel estrogens and their radical scavenging effects, iron-chelating, and total antioxidative activities: 17α-substituted analogs of Δ9(11)-dehydro-17 β-estradiol

Ionic hydrogenation of 3-methoxy-14α,15α-methylenestra-1,3,5(10),8-tetraen-17α-ol: A correction

Synthesis of 13-ethyl-11-methylene-18,19-dinor-17α-pregn-4-en-20-yn-17-ol (desogestrel) and its main metabolite 3-oxo desogestrel

Synthesis of (1S,4R)-(-)-4-Hydroxy-2-cyclopentenyl Acetate by a Highly Enantioselective Enzyme-Catalyzed Transesterification in Organic Solvents

2,2-disubstituierte cyclopentan-1,3-dione—2

2,2-disubstituierte cyclopentan-1,3-dione—2: Untersuchung der regioselektivität von alkylierungs-reaktionen an 2-methyl-cyclopentan-1,3-dion

Steroide. XII [1]. Steroid-alkansulfonate

Sterode. VIII. Darstellung Racemischer und enantiomerer 19-Norsteroide

Syntheses and Reactions of 2,2-Disubstituted Cyclopentane-1,3-diones, 6. Conversion of 2-Methylcyclopentane-1,3-dione into 5-Methylcycloheptane-1,4-dione via 3-(1-Methyl-2,5-dioxocyclopentyl)propanal

Die Bestimmung der Optischen Reinheit an Zwischenprodukten der Prostaglandinsynthese mit Hilfe der NMR-Spektroskopie

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