54878-25-0

Usage

Uses

Used in Pharmaceutical Industry:
(2R,6R)-6,10-dimethyl-2-prop-1-en-2-yl-spiro[4.5]dec-9-en-8-one is used as a potential pharmaceutical compound for its unique structural properties and potential interactions with biological targets. Its cyclic ketone structure and specific substitutions may allow it to modulate various biological pathways, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (2R,6R)-6,10-dimethyl-2-prop-1-en-2-yl-spiro[4.5]dec-9-en-8-one can be used as a starting material or a building block for the synthesis of more complex molecules with specific biological activities. Its unique structure may provide insights into the design and development of novel compounds with tailored properties for various applications.
Used in Material Science:
The unique structural features of (2R,6R)-6,10-dimethyl-2-prop-1-en-2-yl-spiro[4.5]dec-9-en-8-one may also find applications in material science, where it could be used to develop new materials with specific properties, such as improved stability, reactivity, or selectivity in various chemical processes.

InChI:InChI=1/C15H22O/c1-10(2)13-5-6-15(9-13)11(3)7-14(16)8-12(15)4/h7,12-13H,1,5-6,8-9H2,2-4H3/t12-,13-,15?/m1/s1

Upstream product

• 137941-79-8 (-)-(2R,5S,10R)-2-isopropenyl-6,10-dimethylspiro<4.5>dec-6-ene 
• 75-24-1 trimethylaluminum 
• 61167-63-3 (+)-(2R,5S)-2-isopropenyl-6-methylspiro-[4.5]dec-6,9-dien-8-one 
• 74411-02-2 (-)-(6S,9R)-9-isopropenyl-6-methylbicyclo<4.4.0>deca-1,4-dien-3-one 
• 79265-84-2 (2R^*,5S^*,10R^*)-2-(3-chloropropen-2-yl)-6,10-dimethylspiro<4.5>dec-6-en-8-one ethylene dithioacetal 
• 79265-83-1 (2R^*,5S^*,10R^*)-2-(3-hydroxypropen-2-yl)-6,10-dimethylspiro<4.5>dec-6-en-8-one ethylene dithioacetal 
• 79265-82-0 (2R^*,5S^*,10R^*)-2-(1-ethoxycarbonylvinyl)-6,10-dimethylspiro<4.5>dec-6-en-8-one ethylene dithioacetal 
• 79265-81-9 2-((8S,10R,13R)-7,13-Dimethyl-1,4-dithia-dispiro[4.2.4.2]tetradec-6-en-10-yl)-malonic acid monoethyl ester 
• 79265-80-8 (2R^*,5S^*,10R^*)-2-bis(ethoxycarbonyl)methyl-6,10-dimethylspiro<4.5>dec-6-en-8-one ethylene dithioacetal 
• 79276-44-1 (2S^*,5S^*,10R^*)-2-mesyloxy-6,10-dimethylspiro<4.5>dec-6-en-8-one ethylene dithioacetal 
• 73879-11-5 4-(2,2-ethylenedioxyethyl)-3,5-dimethyl-5,6-dihydroanisole 
• 78657-68-8 Methanesulfonic acid 2-[(1R,4S)-5-(1-hydroxy-1-methyl-ethyl)-4-methoxy-2,7-dimethyl-bicyclo[2.2.2]oct-2-en-1-yl]-ethyl ester 
• 73879-12-6 (1S,2S,4R)-4-[1,3]Dioxolan-2-ylmethyl-1-methoxy-5,8-dimethyl-bicyclo[2.2.2]oct-5-ene-2-carboxylic acid methyl ester 
• 73879-12-6 (1S,2R,4R)-4-[1,3]Dioxolan-2-ylmethyl-1-methoxy-5,8-dimethyl-bicyclo[2.2.2]oct-5-ene-2-carboxylic acid methyl ester 

Downstream Products

• 35951-50-9 (+)-lubimin 
• 103573-06-4 oxysolavetivone 

Relevant academic research and scientific papers

NOVEL METHODS FOR PRODUCTION OF 5-EPI-β-VETIVONE, 2-ISOPROPYL-6,10-DIMETHYL-SPIRO[4.5]DECA-2,6-DIEN-8-ONE, AND 2-ISOPROPYL-6,10-DIMETHYL-SPIRO[4.5]DECA-1,6-DIEN-8-ONE

The present invention is directed to novel methods for production of 5-epi-β-vetivone, 2-isopropyl-6,10-dimethyl-spiro[4.5]deca-2,6-dien-8-one and 2-isopropyl-6,10-dimethyl-spiro[4,5]deca-1,6-dien-8-one, which are useful for their fragrant qualities, in one embodiment the present invention describes a method for production of 5-epi-β-vetivone by the use of premnaspirodiene as starting material. In another embodiment the present invention describes a method for production of 2-isopropyl-6,10-dimethyl- spiro[4.5]deca-2,6-dien-8-one and 2-isopropyl-6,10-dimethyl-spiro[4.5]deca-1,6-dien-8-one by the use of premnaspirodiene as starting material. In yet another embodiment the present invention describes a novel method for production of premnaspirodiene from a terpene substrate.

Total synthesis of (-)-solavetivone using enantioselective copper-catalysed conjugate addition of Me3Al to a cyclohexa-2,5-dienone intermediate

By applying a new enantioselective Cu-catalysed conjugate addition of Me3Al, (-)-solavetivone 1 is synthesized stereoselectively from cyclohexa-2,5-dienone 4, prepared from a chiral compound 6 using a regioselective HgII-mediated cyc

A General Synthetic Approach of Spirovetivanes. The Synthesis of (+/-)-Solavetivone, (+/-)-Hinesol, and Related Compounds

The synthetic procedure leading to preparation of representative compounds, (+/-)-solavetivone and (+)-hinesol, of two classes of spirovetivanes, is described.The procedure involves Diels-Alder reaction of 4-substituted 5,6-dihydro-3,5-dimethylanisoles wi

Π-CYCLIZATION: THE SYNTHESIS OF (+/-)-SOLAVETIVONE AND (+/-)-HINESOL

A general efficient approach leading to the total synthesis of (+/-)-solavetivone, (+/-)-hinesol, and related spirovetivanes, is described.The process involves stereoselective formation of the asymmetric center at C-7 by ?-cyclisation as a key step.

Total Synthesis of (+/-)-Solavetivone; X-Ray Crystal Structure of 2-Hydroxy-6,10-dimethylspirodec-6-en-8-one

(+/-)-Solavetivone (1) was synthesized by a new spiro-annelation reaction and a unique regio- and stereoselective reduction of the spiro-dienone (4) to give (5), the structure of which has been determined by X-ray crystallography.