72601-35-5

Usage

InChI:InChI=1/C15H20O2/c1-14(2)5-10-12(6-14)15(3)4-9-7-16-8-11(9)13(10)17-15/h7-8,10,12-13H,4-6H2,1-3H3/t10-,12+,13+,15+/m1/s1

Upstream product

• 201230-82-2 carbon monoxide 
• 121012-88-2 (1S,8S)-8-Methyl-4,11-dioxa-tricyclo[6.2.1.0^2,6]undeca-2,5,9-triene 
• 74-99-7 prop-1-yne 
• 74-88-4 methyl iodide 
• 89002-38-0 (4S,4aR,7aS)-6,6-Dimethyl-8-methylene-4,4a,5,6,7,7a,8,9-octahydro-2-oxa-cyclopenta[f]azulen-4-ol 
• 35008-20-9 4,4α,5,6,7,7α,8,9-octahydro-4,8-dihydroxy-6,6,8-trimethyl-(4S,4αR,7αS,8S)-azuleno[5,6-c]furan-1(3H)-one 
• 59684-34-3 furandiol 
• 127818-25-1 (1S,5S)-4-[1-Butylsulfanyl-meth-(Z)-ylidene]-1-methyl-8-oxa-bicyclo[3.2.1]oct-6-en-3-one 
• 127818-25-1 (1S,5S)-4-[1-Butylsulfanyl-meth-(E)-ylidene]-1-methyl-8-oxa-bicyclo[3.2.1]oct-6-en-3-one 
• 73350-65-9 (1R^*,5S^*)-1-methyl-8-oxabicyclo<3.2.1>oct-6-en-3-one 
• 127786-92-9 (1S,5S)-4-[1-Hydroxy-meth-(Z)-ylidene]-1-methyl-8-oxa-bicyclo[3.2.1]oct-6-en-3-one 

Relevant academic research and scientific papers

3,8-ETHERS OF LACTARANE SESQUITERPENES

An ethanol extract of Lactarius necator gave 3,8-oxa-13-hydroxy-lactar-6-en-5-oic acid γ-lactone and furanether A, besides other known sesquiterpenes.Syntheses of these internal ethers, as well as the 13-oxa-lactonic analogue, were performed.The antifeedant properties of the internal ethers measured against the storage pests Tribolium confusum, Trogoderma granarium and Sitophylus granarius are reported.Key Word Index: Lactarius necator; Basidiomycetes; fruiting body, lactarane 3,8-ethers; antifeedant activity, storage pests: Tribolium confusum, Trogoderma granarium, Sitophylus granarius.

EFFICIENT SYNTHETIC ENTRY TO OXYGEN-BRIDGED LACTARANES USING ORGANOMETALLIC METHODOLOGY: A SHORT SYNTHESIS OF FURANETHER B

A 9-step synthesis of the sesquiterpene furanether B from 2-methylfuran is described; the furan moiety is carried through the last 5 steps, which include Pauson-Khand cycloaddition, the key to the synthesis.

THE STRUCTURE OF A NOVEL SESQUITERPENE FURAN ALCOHOL WITH A LACTARANE SKELETON

The exomethylene furan alcohol 2, which is formed when fatty acid esters of velutinal 1 isolated from Lactarius species are degraded on silica gel, correlates the absolute configuration of isovelleral 5a with that of other sesquiterpenes isolated from Lactarius sp.

BIOGENESIS-LIKE CONVERSION OF MARASMANE TO LACTARANE AND SECO-LACTARANE SKELETON

Some sesquiterpene furans with lactarane and seco-lactarane skeletons which previously have been isolated from many Lactarius and Russula species, were chemically derived from stearyl velutinal via a transformation similar to the biosynthetic pathway.