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Journal ArticleDOI

The stereospecific synthesis of inotodiol 3β, 22R-dihydroxylanosta-8,24-diene

J. P. Poyser, +2 more
- 01 Jan 1974 - 
- Vol. 30, Iss: 8, pp 977-986
TLDR
Inotodiol 1a has been stereospecifically synthesised from lanosterol in six steps and Horeau's method utilised to demonstrate the R-configuration at C-22.
About
This article is published in Tetrahedron.The article was published on 1974-01-01. It has received 17 citations till now. The article focuses on the topics: Inotodiol & Lanosterol.

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Citations
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Book ChapterDOI

Experimental approaches to antifungal chemotherapy.

TL;DR: This chapter discusses the experimental approaches to antifungal chemotherapy, and the possibility exists of applying a topical treatment to the affected area, or alternatively treating the infection systemically, getting the parasite from “behind.
Journal ArticleDOI

Dormantinol, a possible precursor in solanidine biosynthesis, from budding Veratrum grandiflorum

TL;DR: A new sapogenin, dormantinol, was isolated from budding Veratrum, and identified as (25S)-cholest-5-ene-3β,22α,26-triol by spectral analysis and its synthesis from dormantinone.
Journal ArticleDOI

General and highly α-regioselective zinc-mediated prenylation of aldehydes and ketones.

TL;DR: The method provides a convenient route for the direct α-prenylation of carbonyl compounds in a highly α-regioselective manner using a cheap and convenient mediator.
Journal ArticleDOI

Guaianolides, heliangolides, diterpenes and cycloartenol derivatives from Balsamorhiza sagittata

TL;DR: In this paper, the aerial parts of Balsamorhiza sagittata were investigated for the extraction of sesquiterpene lactones, five guaianolides, three heliangolides and three germacranolides.
Journal Article

Chemical Constituents of Inonotus obliquus I.:A new triterpene, 3β-hydroxy-8,24-dien-lanosta-21,23-lactone from sclerotium

TL;DR: A new lanostane type triterpene with a lactone partial structure in the side chain was isolated from the sclerotium of the wood rotting fungus Inonotus ob/iquus together with three known compounds; lanosterol, inotodiol and trametenolic acid.
References
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Journal ArticleDOI

Zur Chemie des Ecdysons, VII: Die Kristall‐ und Molekülstrukturanalyse des Insektenverpuppungshormons Ecdyson mit der automatisierten Faltmolekülmethode

TL;DR: In this article, the vollstandige Struktur und Konfiguration des Insektenverpuppungshormons Ecdyson wird durch Rontgenstrukturanalyse der naturlichen, schweratomfreien Verbindung als 2β.3β.14α.22βF.25-Pentahydroxy-Δ7-5β-cholestenon-(6) ermittelt.
Journal ArticleDOI

Determination des configurations par “dedoublement partiel”—III : Alcools steroides

TL;DR: The methode de dedoublement partiel as discussed by the authors is a partiel partiel (1) a ete appliquee a des alcools steroides tres varies and elle permet de trouver avec la plus grande surete la configuration α ou β de l'hydroxyle for toutes les positions examinees, exception faite des positions 2, 3 and 16 qui, en l'absence de substituants vicinaux, ne donnent lieu qu'a de faibles dedoublements.
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