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(Z)-3α-(1,3-Dioxoisoindolin-2-yl)-17(20)-pregnene.

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TLDR
The title compound, C29H37NO2, crystallized with two independent molecules in an asymmetric unit in which the conformation of the cyclohexyl ring of the pregnene moiety bonded to the 3α-(1,3-dioxoisoindolin-2-yl)- ring system differs: in one molecule it is in a chair conformation, while in the other it exhibits a half-chair conformation.
Abstract
The title compound, C29H37NO2, crystallized with two independent mol­ecules in an asymmetric unit in which the conformation of the cyclo­hexyl ring of the pregnene moiety bonded to the 3α-(1,3-dioxoisoindolin-2-yl)- ring system differs: in one mol­ecule it is in a chair conformation, while in the other it exhibits a half-chair conformation. The other six-membered rings in the pregnene moiety are in chair conformations and the five-membered rings are in envelope forms in both mol­ecules. In both mol­ecules, the 3α-(1,3-dioxoisoindolin-2-yl)- ring systems are individually approximately planar, with r.m.s. devtaions 0.0148 and 0.0264 A. The structure is consolidated by inter­molecular C—H⋯O hydrogen-bonding inter­actions involving the carbonyl O atoms and methyl, methyl­ene and methyl­idyne groups, resulting in a two-dimensional structure.

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(Z)-3β-(2-Chloro-anilino)-17(20)-pregnene.

TL;DR: In the pregnene fragment of the title compound, C27H38ClN, the three six- Membered rings exhibit chair conformations and the five-membered ring has a distorted envelope form with the fused C atom not bearing a methyl group as the flap atom.
References
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Journal ArticleDOI

A short history of SHELX

TL;DR: This paper could serve as a general literature citation when one or more of the open-source SH ELX programs (and the Bruker AXS version SHELXTL) are employed in the course of a crystal-structure determination.
Journal ArticleDOI

Ladroside (= 6′-Caffeoyl-mussaenoside), a New Iridoid Glucoside from Veronica officinalis L. (Scrophulariaceae) and the elucidation of the absolute configuration at C(8) of mussaenoside

TL;DR: A new iridoid glucoside, named ladroside, together with mussaenoside (1) [2], has been isolated from Veronica officinalisL..
Journal ArticleDOI

Pregnane alkaloids from Pachysandra axillaris

TL;DR: Nine new pregnane alkaloids, pachysamines J-R (1-9), together with seven known ones, were isolated from Pachysandra axillaris by spectroscopic methods and showed moderate activities against A-549, SK-BR-3, and PANC-1 cells.
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