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Synthesis and activity evaluation of a series of cholanamides as modulators of the liver X receptors

Bioorganic & medicinal chemistry, 2018-03, Vol.26 (5), p.1092-1101

2018

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Antiproliferative activity of synthetic naphthoquinones related to lapachol. First synthesis of 5-hydroxylapachol

Bioorganic & medicinal chemistry, 2010-04, Vol.18 (7), p.2621-2630

2010

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Oxido-bridged neurosteroid analogues. Synthesis of 2,19-oxido-allopregnanolone

ARKIVOC, 2003-10, Vol.2003 (10), p.468-476

2003

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Intramolecular PhIO Mediated Copper-Catalyzed Aziridination of Unsaturated Sulfamates: A New Direct Access to Polysubstituted Amines from Simple Homoallylic Alcohols

Organic letters, 2002-07, Vol.4 (15), p.2481-2483

2002

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Self-assembly of a silylated steroid-based organogelator and its use as template for the in situ sol–gel polymerization of tetraethyl orthosilicate

Tetrahedron, 2010-03, Vol.66 (12), p.2162-2167

2010

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27-Nor-Δ4-dafachronic acid is a synthetic ligand of Caenorhabditis elegans DAF-12 receptor

Bioorganic & medicinal chemistry letters, 2013-05, Vol.23 (10), p.2893-2896

2013

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Withanolides and Related Steroids

Progress in the Chemistry of Organic Natural Products Vol. 94, 2011, Vol.94, p.127-229

2011

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Synthesis of C–C bonded dimeric steroids by olefin metathesis

Tetrahedron, 2009-05, Vol.65 (18), p.3615-3623

2009

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Synthesis and GABAA receptor activity of 2,19-sulfamoyl analogues of allopregnanolone

Bioorganic & medicinal chemistry, 2009-09, Vol.17 (18), p.6526-6533

2009

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Synthesis of 6-thia analogs of the natural neurosteroid allopregnanolone

Tetrahedron, 2006-05, Vol.62 (20), p.4762-4768

2006

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Biological activity and ligand binding mode to the progesterone receptor of A-homo analogues of progesterone

Bioorganic & medicinal chemistry, 2011-03, Vol.19 (5), p.1683-1691

2011

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Synthesis and GABA A receptor activity of oxygen-bridged neurosteroid analogs

Bioorganic & medicinal chemistry, 2008-04, Vol.16 (7), p.3831-3838

2008

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Synthesis of 6,19-Sulfamidate Bridged Pregnanes

Journal of organic chemistry, 2005-10, Vol.70 (21), p.8613-8616

2005

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6,19-carbon-bridged steroids. Synthesis of 6,19-methanoprogesterone

Organic & biomolecular chemistry, 2003-03, Vol.1 (6), p.939-943

2003

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Synthesis of C(1)–C(11) oxygen-bridged pregnanes

Tetrahedron letters, 2005-06, Vol.46 (24), p.4235-4238

2005

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PhINSes mediated aziridination of 11-pregnane derivatives: synthesis of an 11,12-aziridino analogue of neuroactive steroids

Tetrahedron, 2003-02, Vol.59 (7), p.1009-1014

2003

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Synthesis and GABA A receptor activity of a 6,19-Oxido analogue of pregnanolone

Bioorganic & medicinal chemistry letters, 2003-02, Vol.13 (3), p.343-346

2003

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Synthesis of 6,19-cyclopregnanes. Constrained analogues of steroid hormones

Organic & biomolecular chemistry, 2007-01, Vol.5 (15), p.2453-2457

2007

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Aziridination of 11-pregnene-3,20-dione using PhIN-Ses

Tetrahedron letters, 2000-09, Vol.41 (36), p.7041-7045

2000

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Ring expansion of fused cyclopropylketones. Synthesis of a 12(13→18)- abeo-pregnane

Tetrahedron letters, 1996-02, Vol.37 (7), p.929-932

1996

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Oxidative Cyclization of Iodo Ketones. Synthesis of 6-Oxa-5α-pregnane-3,20-dione

Journal of organic chemistry, 1996-09, Vol.61 (19), p.6673-6677

1996

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Rearrangement of 18-iodo- and 20-iodopregnanes mediated by iodosyl derivatives

Perkin 1 : an international journal of organic and bio-organic chemistry, 2001 (13), p.1511-1517

2001

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An Improved Preparation of 11,19-Oxidopregn-4-ene-3,20-dione and 6,19-Oxidopregn-4-ene-3,11,20-trione

Zeitschrift für Naturforschung. B, A journal of chemical sciences, 1990-05, Vol.45 (5), p.711-716

1990

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Simple synthetic approach to 6-oxa steroids. Synthesis of 6-oxa-5β-pregnane-3,20-dione

J. Chem. Soc., Perkin Trans. 1, 1995 (9), p.1089-1093

1995

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Mercuric Oxide-Iodine Oxidation of 6β-Hydroxypregnanes. Influence of the C-5 Functionality

Zeitschrift für Naturforschung. B, A journal of chemical sciences, 1988-04, Vol.43 (4), p.491-496

1988

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Synthesis and activity evaluation of a series of cholanamides as modulators of the liver X receptors

Antiproliferative activity of synthetic naphthoquinones related to lapachol. First synthesis of 5-hydroxylapachol

Oxido-bridged neurosteroid analogues. Synthesis of 2,19-oxido-allopregnanolone

Intramolecular PhIO Mediated Copper-Catalyzed Aziridination of Unsaturated Sulfamates: A New Direct Access to Polysubstituted Amines from Simple Homoallylic Alcohols

Self-assembly of a silylated steroid-based organogelator and its use as template for the in situ sol–gel polymerization of tetraethyl orthosilicate

27-Nor-Δ4-dafachronic acid is a synthetic ligand of Caenorhabditis elegans DAF-12 receptor

Withanolides and Related Steroids

Synthesis of C–C bonded dimeric steroids by olefin metathesis

Synthesis and GABAA receptor activity of 2,19-sulfamoyl analogues of allopregnanolone

Synthesis of 6-thia analogs of the natural neurosteroid allopregnanolone

Biological activity and ligand binding mode to the progesterone receptor of A-homo analogues of progesterone

Synthesis and GABA A receptor activity of oxygen-bridged neurosteroid analogs

Synthesis of 6,19-Sulfamidate Bridged Pregnanes

6,19-carbon-bridged steroids. Synthesis of 6,19-methanoprogesterone

Synthesis of C(1)–C(11) oxygen-bridged pregnanes

PhINSes mediated aziridination of 11-pregnane derivatives: synthesis of an 11,12-aziridino analogue of neuroactive steroids

Synthesis and GABA A receptor activity of a 6,19-Oxido analogue of pregnanolone

Synthesis of 6,19-cyclopregnanes. Constrained analogues of steroid hormones

Aziridination of 11-pregnene-3,20-dione using PhIN-Ses

Ring expansion of fused cyclopropylketones. Synthesis of a 12(13→18)- abeo-pregnane

Oxidative Cyclization of Iodo Ketones. Synthesis of 6-Oxa-5α-pregnane-3,20-dione

Rearrangement of 18-iodo- and 20-iodopregnanes mediated by iodosyl derivatives

An Improved Preparation of 11,19-Oxidopregn-4-ene-3,20-dione and 6,19-Oxidopregn-4-ene-3,11,20-trione

Simple synthetic approach to 6-oxa steroids. Synthesis of 6-oxa-5β-pregnane-3,20-dione

Mercuric Oxide-Iodine Oxidation of 6β-Hydroxypregnanes. Influence of the C-5 Functionality

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