69301-25-3

Usage

InChI:InChI=1/C15H22O2/c1-10(2)6-5-7-11(3)13-9-14(16)12(4)8-15(13)17/h6,8-9,11,16-17H,5,7H2,1-4H3/t11-/m1/s1

Upstream product

• 670260-38-5 (R)-(-)-curcuquinone 
• 78920-00-0 1-(2,5-dimethoxy-4-methylphenyl)ethyl diisopropylcarbamate 
• 1597450-22-0 2-[(1R)-1,5-dimethylhex-4-en-1-yl]-4-(β-D-glucopyranosyloxy)-5-methylphenyl β-D-glucopyranoside 
• 59684-62-7 (R)-(-)-xanthorrhizol 
• 196193-23-4 4-[(1R)-1,5-dimethylhex-4-enyl]cyclohex-2-en-1-one 
• 915301-61-0 2-methyl-5-((R)-6-methylhept-5-en-2-yl)cyclohex-3-ene-1,2-diol 
• 915235-16-4 6-hydroxy-4-((R)-6-methylhept-5-en-2-yl)cyclohex-2-enone 
• 915235-17-5 2-methyl-5-((R)-6-methylhept-5-en-2-yl)-4-oxocyclohex-2-enyl acetate 
• 915301-62-1 2-hydroxy-2-methyl-5-((R)-6-methylhept-5-en-2-yl)cyclohex-3-enyl acetate 

Downstream Products

• 923602-60-2 C₂₉H₃₄O₂ 
• 923602-61-3 C₂₉H₃₆O₄ 
• 923602-52-2 C₂₉H₃₆O₄ 
• 670260-38-5 (R)-(-)-curcuquinone 

Relevant academic research and scientific papers

New bisabolane sesquiterpenes from the rhizomes of Curcuma xanthorrhiza Roxb. and their inhibitory effects on UVB-induced MMP-1 expression in human keratinocytes

Two new bisabolane sesquiterpenoids, 1 and 2, along with five known ones, 13-hydroxyxanthorrhizol (3), 12,13-epoxyxanthorrhizol (4), xanthorrhizol (5), β-curcumene (6), and β-bisabolol (7), were isolated from the rhizomes of Curcuma xanthorrhiza Roxb. The

Application of the lithiation-borylation reaction to the rapid and enantioselective synthesis of the bisabolane family of sesquiterpenes

The expedient enantioselective synthesis of 5 bisabolane sesquiterpenes has been achieved using a common, one-pot lithiation-borylation reaction of secondary benzylic carbamates and either protodeboronation or oxidation to give the natural products in few

Chemistry of xanthorrhizol: synthesis of several bisabolane sesquiterpenoids from xanthorrhizol

(-)-Xanthorrhizol (1) isolated from the rhizomes of Curcuma xanthorrhiza has been transformed to several bisabolane-type sesquiterpenoids, in a stereoselective manner. 10R- and 10S-10,11-dihydro-10,11-dihydroxyxanthorrhizols (2, 3), (-)-curcuquinone (4),

First enantiospecific synthesis of (-)-parvifoline and (-)-curcuquinone

The first enantiospecific synthesis of (-)-parvifoline, employing ring-closing metathesis as the key step, and (-)-curcuquinone from naturally occurring (R)-(+)-citronellal is described.