56857-64-8

Usage

InChI:InChI=1/C15H24O3/c1-12(2,16)11-5-6-13(3)10-18-14(4)7-8-17-15(13,14)9-11/h7-8,11,16H,5-6,9-10H2,1-4H3/t11-,13+,14-,15?/m1/s1

Upstream product

• 68962-07-2 4,6β-dimethyl-6α-formyl-9β-(2-hydroxy-2-methyl)ethyl-1-oxaspiro<4.5>dec-3-en-2-one 
• 76192-86-4 [(1S,2S,5R)-2-Benzyloxymethyl-5-(1-benzyloxy-1-methyl-ethyl)-1-hydroxy-2-methyl-cyclohexyl]-propynoic acid ethyl ester 
• 76192-83-1 (5S,6S,9R)-6-Benzyloxymethyl-9-(1-benzyloxy-1-methyl-ethyl)-4,6-dimethyl-1-oxa-spiro[4.5]dec-3-en-2-one 
• 497-62-1 (-)-2-carone 
• 76192-81-9 (2S,5R)-2-Benzyloxymethyl-5-(1-benzyloxy-1-methyl-ethyl)-2-methyl-cyclohexanone 
• 76207-98-2 (1S,3S,6R)-3-Benzyloxymethyl-3,7,7-trimethyl-bicyclo[4.1.0]heptan-2-one 
• 24405-57-0 β-rotunol 
• 68962-04-9 1β-hydroxy-β-rotunol 
• 37209-50-0 (4R,5R)-1,4:2,5-diepoxy-1,2-secoeudesm-2-en-11-yl acetate 
• 76192-84-2 (5S,6S,9R)-6-Hydroxymethyl-9-(1-hydroxy-1-methyl-ethyl)-4,6-dimethyl-1-oxa-spiro[4.5]dec-3-en-2-one 

Downstream Products

• 37209-50-0 (4R,5R)-1,4:2,5-diepoxy-1,2-secoeudesm-2-en-11-yl acetate 

Relevant academic research and scientific papers

Biosynthesis of Phytuberin

Feeding experiments with (+/-)-solavetivone in diseased potato tuber tissues indicated that phytuberin, one of the most representative phytoalexins in the Solanaceae, was biosynthesized from solavetivone.

Synthesis of Phytuberin

The first synthesis of phytuberin, which mimics the proposed biogeneses in critical stages, is described.The synthesis also establishes the absolute configuration.