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Stereocontrolled Synthesis of 3-Acyl-4-alkoxy-5-aryl-1,2,4(E)-pentatrienes and Their Subsequent Electrocyclization to Naphthalenes

Philip Turnbull, +1 more
- 01 Jun 1995 - 
- Vol. 60, Iss: 11, pp 3274-3275
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This article is published in Journal of Organic Chemistry.The article was published on 1995-06-01. It has received 22 citations till now. The article focuses on the topics: Alkoxy group & Aryl.

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The application of cyclobutane derivatives in organic synthesis.

TL;DR: Transformation of Cyclobutane Derivatives inNatural Product Syntheses: A Review of the Transformations in Organic Syntheses.
Journal ArticleDOI

Gold-catalyzed hydroarylation of allenes: a highly regioselective carbon-carbon bond formation producing six-membered rings.

TL;DR: Gold-catalyzed intramolecular hydroarylation of allenic anilines and phenols offers an efficient route to dihydroquinoline and chromene derivatives under mild reaction conditions, leading to a highly selective formation of six-membered rings.
Journal ArticleDOI

Total syntheses of carazostatin and hyellazole by allene-mediated electrocyclic reaction

TL;DR: The free radical scavenger carazostatin and the marine alkaloid hyellazole have been synthesized by a new type of allene-mediated electrocyclic reaction involving the indole 2,3-bond as a key step.
Journal ArticleDOI

Copper-catalyzed tandem alkynylation, propargyl–allenyl isomerization, 6π-electrocyclization of Morita–Baylis–Hillman adducts to naphthalenes

TL;DR: In this article, an expedient synthetic approach of naphthalenes was developed by the reaction of Morita-Baylis-Hillman bromides and arylacetylenes.
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