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Journal ArticleDOI

A New Synthesis of 4-Methylene-10-methyl-Δ8,9-carbomethoxy-trans-decalin

TLDR
A novel synthesis of the title compound has been accomplished starting with alcohol (3) which in turn was prepared from the Wieland-Miescher ketone (1), which after reduction, mesylation, and demesylation afforded the unsaturated ester as discussed by the authors.
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This article is published in Synthetic Communications.The article was published on 2003-06-01. It has received 2 citations till now. The article focuses on the topics: Wittig reaction & Ketone.

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Citations
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Journal ArticleDOI

Wittig Reaction on 5,8-Dimethyl-2-Tetralone. A Total Formal Synthesis of Emmotin-G Methyl Ether

TL;DR: In this paper, the conversion of tetralone 2 to 6methoxy-7-acetyl-1,4-dimethylnaphthalene 7, a precursor for Emmotin-G methyl ether is described.
Journal ArticleDOI

A New Synthesis of 4-Methylene-10-methyl-Δ8,9-carbomethoxy-trans-decalin.

TL;DR: A novel synthesis of the title compound has been accomplished starting with alcohol (3) which in turn was prepared from the Wieland-Miescher ketone (1), which after reduction, mesylation, and demesylation afforded the unsaturated ester.
References
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Book

Studies in natural products chemistry

TL;DR: The series covers the synthesis or testing and recording of the medicinal properties of natural products, providing cutting edge accounts of the fascinating developments in the isolation, structure elucidation, synthesis, biosynthesis and pharmacology of a diverse array of bioactive natural products.
Book

Applications of nuclear magnetic resonance spectroscopy in organic chemistry

TL;DR: In this paper, the authors discuss the applications of nuclear magnetic resonance spectroscopy in organic chemistry and propose a fast and easy way to obtain a book for such applications, taking into account that the book can straight get it.
Journal ArticleDOI

Reductive cleavage of benzyl ethers with lithium naphthalenide. A convenient method for debenzylation

TL;DR: An operationally simple, high-yielding and highly chemoselective procedure has been developed for the conversion of benzyl ethers to the corresponding alcohols, using lithium naphthalenide as the reagent.
Journal ArticleDOI

Potent army worm antifeedants from the east African Warburgia plants

TL;DR: Chemical investigation of antifeedant compounds from Warburgia plants has led to the isolation and characterization of polygodial, ugandensidial, and the unknown warburganal, which exhibit very strong antifeEDant activity against the African army worm.
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