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Relevant bibliographies by topics / 3-Furylamines

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Academic literature on the topic '3-Furylamines'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "3-Furylamines"

1

Lingham, Anthony R., Trevor J. Rook, and Helmut M. Hügel. "Synthesis of Some 3-Furylamine Derivatives." Australian Journal of Chemistry 55, no. 12 (2002): 795. http://dx.doi.org/10.1071/ch02178.

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A general and efficient method for the synthesis of 3-furylamines via Michael addition of amines to acyclic keto alkynol precursors has been achieved. The preparation of various 3-furylamines has been carried out using a flexible methodology which also allows modification of the substituent at the 5-position.

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2

Lingham, Anthony R., Helmut M. Hügel, and Trevor J. Rook. "Diels - Alder Reactions of 3-Furylamines in Organic and Aqueous Solvents." Australian Journal of Chemistry 59, no. 5 (2006): 336. http://dx.doi.org/10.1071/ch05339.

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Various 5-methyl-3-aminofurans have been shown to undergo facile Diels–Alder reactions with methyl acrylate in aqueous media. Reactions proceeded with exclusive regiochemistry, and enamine cycloadducts were readily hydrolyzed to afford 7-oxabicyclo[2.2.1]heptanones in high yields.

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3

Lingham, Anthony R., Helmut M. Hügel, and Trevor J. Rook. "Studies Towards the Synthesis of Salvinorin A." Australian Journal of Chemistry 59, no. 5 (2006): 340. http://dx.doi.org/10.1071/ch05338.

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Salvinorin A 1, a psychoactive neoclerodane diterpenoid from the Mexican sage S. divinorum, has gained interest as a selective κ-opioid receptor agonist. Non-racemic 3-furylamines 9a and 9b have been prepared from (+)-pseudoephedrine and (–)-ephedrine for application in the stereoselective synthesis of the ketone ring of 1. Diels–Alder reaction of 9b with methyl acrylate in aqueous media, followed by selective ether bridge cleavage, has allowed access to the cyclohexenone 17 with preservation of stereochemistry at C2. A model route to the lactone ring has also been achieved through a one-pot d

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4

Jones, P. G., and N. K. Keweloh (née Homsy). "N,N-Diethyl-4-[2,2,4,4-tetrakis(trifluoromethyl)-2H,4H-1,3,5-dioxazin-6-ylthio]-2,2,5,5-tetrakis(trifluoromethyl)-2,5-dihydro-3-furylamine." Acta Crystallographica Section C Crystal Structure Communications 44, no. 7 (July 15, 1988): 1315–17. http://dx.doi.org/10.1107/s0108270188002926.

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5

Lingham, Anthony R., Helmut M. Huegel, and Trevor J. Rook. "Diels—Alder Reactions of 3-Furylamines in Organic and Aqueous Solvents." ChemInform 37, no. 43 (October 24, 2006). http://dx.doi.org/10.1002/chin.200643122.

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Dissertations / Theses on the topic "3-Furylamines"

1

Lingham, Anthony, and arlingham@hotmail com. "Studies Toward the Synthesis of Salvinorin A." RMIT University. Applied Sciences, 2008. http://adt.lib.rmit.edu.au/adt/public/adt-VIT20080428.095126.

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Salvinorin A [(2S,4aR,6aR,7R,9S,10aS,10bR)-9-(acetyloxy)-2-(3-furanyl)-dodecahydro-6a,10b-dimethyl-4,10-dioxo-2H-naptho[2,1-c]pyran-7-carboxylic acid methyl ester] is a trans-neoclerodane diterpene from the leaves of the hallucinogenic Mexican sage Salvia divinorum and has been identified as the principal psychoactive component in this plant of traditional spiritual importance. Salvinorin A is the most potent naturally occurring hallucinogen found so far and is reported to act selectively as a Û-opioid receptor agonist. Synthetic modification of the natural product has contributed to a number

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