A novel synthetic approach to (20 R)- and (20 S)-21-hydroxy steroids. Synthesis of a marine sterol 21-hydroxycholesterol (original) (raw)

Reduction of 17.alpha.-hydroxy-20-keto steroids: convenient synthesis of (E)-3.beta.-hydroxy-5,17(20)-pregnadiene 3-pivaloate and (Z)-3.beta.,16.alpha.-dihydroxy-5,17(20)-pregnadiene 3-pivaloate

Masato Koreeda

The Journal of Organic Chemistry, 1990

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A new synthesis of 25-hydroxycholesterol

Martin Riediker

Tetrahedron Letters, 1981

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C-24 Stereochemistry of Marine Sterols: (22E)-24-(Isopropenyl)-22-dehydrocholesterol and 24-Isopropenylcholesterol

Yoshinori Fujimoto

CHEMICAL & PHARMACEUTICAL BULLETIN, 2006

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SYNTHESIS OF SOME DIOL DERIVATIVES AS POTENTIAL REAGENTS IN STEROID CHEMISTRY

Katarina Penov Gaši, Evgenija A Djurendić

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An overview of synthetic approaches for heterocyclic steroids

Ritesh Singh

Tetrahedron, 2013

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A rapid and simple one-pot procedure for the synthesis of 3β-acetoxy-5α-hydroxy-6-oxo steroids

Anielka Rosado-Abón, Martin A Iglesias-arteaga

Arkivoc, 2010

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Synthesis of 3β-hydroxy-5α-cholest-8-en-7-one and 3β-hydroxy-5α-cholest-8-en-11-one: Evaluation as potential hypocholesterolemic agents

Kenneth Nusbaum

Steroids, 1986

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A convenient chemoenzymatic synthesis of (1S,7aS)-1-hydroxy-5-oxo-4-(2′-carboxyethyl)-7a-methyltetrahydro-indane—a key intermediate of steroids

Uttam Kalkote

Journal of Molecular Catalysis B: Enzymatic, 2006

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An enantiospecific route to C,D ring synthons for steroid synthesis

Andrew Clase

Canadian Journal of Chemistry, 1992

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A new facile synthesis of steroid dimers containing 17,17 '-dicarboxamide spacers

Rui Carrilho

Tetrahedron Letters, 2013

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27-Hydroxycholesterol, does it exist? On the nomenclature and stereochemistry of 26-hydroxylated sterols

Norman Javitt

Steroids, 2012

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Structure and stereochemistry of (24R)-27-nor-5α-cholestane-3β,4β,5,6α,7β,8,14,15α,24-nonaol: a highly hydroxylated marine steroid from the starfish Archaster typicus

Lelio Mazzarella

Acta Crystallographica Section C-crystal Structure Communications - ACTA CRYSTALLOGR C-CRYST STR, 1988

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Synthetic steroids containing a tertiary butyl group and their biological activities

Lipid Lib

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ChemInform Abstract: Steroids. Part 355. A-Homo-B,19-dinorandrostanes from 6β- Methanesulfonyloxy-5-methyl-19-nor-5β-androst-9-ene Derivatives

Jaroslav Zajícek

ChemInform

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Synthesis of functionalised enantiopure steroids from estrone and cholestanone through organolithium intermediates

Miguel Yus

Tetrahedron: Asymmetry, 2001

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Stereochemically controlled syntheses of 20,22-epoxycholesterols

Masato Koreeda

Tetrahedron Letters, 1976

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A facile approach to steroidal 20-hydroxy-17(20)-en-21-aldehydes: important intermediates in the biological 17-dehydroxylation of C-17 dihydroxyacetone steroids

Maria Luisa Di Gioia

Tetrahedron Letters, 2001

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Steroids: partial synthesis in medicinal chemistry

James Hanson

Natural Product Reports, 2006

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Stereoselective construction of 22-oxygenated steroid side chains by dimethylaluminum chloride-mediated ene reactions of aldehydes

Todd Houston

The Journal of Organic Chemistry, 1993

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Synthesis of (23R)- and (23S)-23H-Isocalysterols, Marine Sterols with a Cyclopropene Moiety in the Side Chain

Kazimierz Minksztym

European Journal of Organic Chemistry, 2000

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Reactions of 5-hydroxy-6-oxo steroids. III. Acid-catalyzed reactions of 3β-acetoxy-5-hydroxy-5α-cholestan-6-one

Jacek Jagodzinski

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Stereocontrolled synthesis of 22-hydroxy-23-acetylenic steroids, key intermediates in steroid side chain construction. Observation of a directive effect by an α-chiral site during asymmetric reduction with -B-3-pinanyl-9-BBN (Alpine-Borane)

Mark Midland

Tetrahedron Letters, 1984

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Synthesis, X-ray crystal structures and biological activity of 16-amino-17-substituted-D-homo steroid derivatives

Katarina Penov Gaši, Srdjan Stojanovic, Evgenija A Djurendić

Steroids, 2003

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First synthesis of a steroid containing an unstable 19-nor-androsta-1,5-dien-3-one system

Anie Philip, Donald Poirier

Tetrahedron, 2006

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