Volume 31, Issue 51
Natural Products
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ChemInform Abstract: Conformational Design for 13α-Steroids.

Bruno Schoenecker

Bruno Schoenecker

Inst. Org. Makromol. Chem., Friedrich-Schiller-Univ., D-07743 Jena, Germany

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Corinna Lange

Corinna Lange

Inst. Org. Makromol. Chem., Friedrich-Schiller-Univ., D-07743 Jena, Germany

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Manuela Koetteritzsch

Manuela Koetteritzsch

Inst. Org. Makromol. Chem., Friedrich-Schiller-Univ., D-07743 Jena, Germany

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Wolfgang Guenther

Wolfgang Guenther

Inst. Org. Makromol. Chem., Friedrich-Schiller-Univ., D-07743 Jena, Germany

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Jennie Weston

Jennie Weston

Inst. Org. Makromol. Chem., Friedrich-Schiller-Univ., D-07743 Jena, Germany

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Ernst Anders

Ernst Anders

Inst. Org. Makromol. Chem., Friedrich-Schiller-Univ., D-07743 Jena, Germany

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Helmar Goerls

Helmar Goerls

Inst. Org. Makromol. Chem., Friedrich-Schiller-Univ., D-07743 Jena, Germany

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First published: 31 May 2010

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

A number of title steroids like (II)—(IX) are prepared as precursors for biologically active compounds and chiral ligands for metal complexation. It is found that the derivatives containing a 17α-substituent or 17-keto group possess the classical steroid conformation, whereas derivatives with a 17β-substituent adopt an atypical C-ring twist-boat and flexible D-ring conformation.

chemical structure image

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