129578-08-1

Basic information

• Product Name: 8-O-acetylgoniotriol
• Synonyms: 8-O-acetylgoniotriol
• CAS NO: 129578-08-1
• Molecular Weight: 292.288
• Mol File: 129578-08-1.mol

Chemical Properties

• CAS DataBase Reference: 8-O-acetylgoniotriol(CAS DataBase Reference)
• NIST Chemistry Reference: 8-O-acetylgoniotriol(129578-08-1)
• EPA Substance Registry System: 8-O-acetylgoniotriol(129578-08-1)

Safety Data

• Hazardous Substances Data: 129578-08-1(Hazardous Substances Data)

Upstream product

• 153619-52-4 (5S,6R,7R,8R)-6-<8-acetoxy-7,8-dihydro-7-(methoxymethoxy)styryl>-5-(methoxymethoxy)-5,6-dihydro-2H-pyran-2-one 
• 162466-16-2 (5S,6R)-5-hydroxy-6-<(1R,2R)-1,2-isopropylidenyloxy-2-phenylethyl>-5,6-dihydropyran-2-one 
• 151830-90-9 4,6-O-Isopropylidene-7-C-phenyl-D-gluco-hept-2-enono-δ-lactone 

Downstream Products

• 153744-08-2 8-epi-altholactone-7-O-acetate 

Relevant articles and documents

Stereocontrolled syntheses of novel styryl lactones, (+)-goniodiol, (+)- goniotriol, (+)-8-acetylgoniotriol, (+)-goniofufurone, (+)-9- deoxygoniopypyrone, (+)-goniopypyrone, and (+)-altholactone from common intermediates and cytotoxicity of their congener

Concise syntheses of (+)-goniodiol, (+)-goniotriol, (+)-8- acetylgoniotriol, (+)-goniofufurone, (+)-9-deoxygoniopypyrone, (+)- goniopypyrone, and (+)-altholactone and their congeners from chiral lactonic aldehydes 27 and 36 as common intermediates are des

Asymmetric total synthesis of antitumor styryl lactones and related natural products

Total synthesis of antitumor styryl lactones based on Sharpless asymmetric dihydroxylation and asymmetric epoxidation starting from methyl cinnamate and cinnamyl alcohol, respectively, was described. Synthesis of the natural asperlin and its related compo

Stereoselective Syntheses of (+)-Goniotriol, (+)-8-Acetylgoniotriol, (+)-Goniodiol, (+)-9-Deoxygoniopypyrone, (+)-Altholactone, and (-)-Goniofupyrone

The γ-lactone intermediate (-)-7, derived from (+)-tricarbonyl(η6-o-(trimethylsilyl)benzaldehyde)chromium(0) complex, was efficiently converted into the corresponding δ-lactone intermediate (-)-11. This second intermediate has been shown to be a versatile compound for stereoselective syntheses of natural styryllactones possessing a six-membered lactone moiety, isolated from Goniothalamus giganteus, by transforming it into (+)-goniotriol, (+)-8-acetylgoniotriol, (+)-goniodiol, (+)-9-deoxygoniopypyrone, (+)-altholactone, and (-)-goniofupyrone.

Enantiospecific Syntheses of (+)-Goniofufurone, (+)-7-epi-Goniofufurone, (+)-Goniobutenolide A, (-)-Goniobutenolide B, (+)-Goniopypyrone, (+)-Altholactone, (+)-Goniotriol, and (+)-7-Acetylgoniotriol

Practical and efficient syntheses of a number of styryl lactones with various structural complexities were accomplished from commercially available and inexpensive D-glycero-D-gulo-heptono-γ-lactone (D-glucoheptonic γ-lactone) (11).Lactone 11 was converte