142955-65-5

Upstream product

• 142955-62-2 (Z)-3-[(4R,5S,6S)-5-Hydroxy-6-((S)-hydroxy-phenyl-methyl)-2,2-dimethyl-[1,3]dioxan-4-yl]-acrylic acid methyl ester 
• 143018-41-1 (Z)-methyl 4,6-O-isopropylidene-7-C-phenyl-L-gluco-hept-2-enoate 
• 142955-64-4 (Z)-Methyl 4,6-O-isopropylidene-7-C-phenyl-D-gluco-hept-2-enoate 
• 944352-99-2 (S)-5-((4R,5R)-5-((R)-hydroxy(phenyl)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)furan-2(5H)-one 
• 134639-65-9 (2,3),(5,6)-bisacetonide-D-gluconic acid methylester 
• 104713-12-4 (1S)-1-phenylprop-2-en-1-ol 
• 1311946-25-4 (S)-5-((4R,5S)-5-((R)-(tert-butyldimethylsilyloxy)(phenyl)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)-furan-2(5H)-one 
• 1311946-23-2 (4R,5S)-5-((4S,5S)-5-((R)-(tertbutyldimethyl-silyloxy)(phenyl)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)-4-hydroxydihydrofuran-2(3H)-one 
• 1311946-21-0 (4R,5S)-4-(benzyloxy)-5-((4S,5S)-5-((R)-(tert-butyldimethylsilyloxy)(phenyl)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)dihydrofuran-2(3H)-one 
• 1311946-06-1 (4R,5S)-4-(benzyloxy)-5-((R)-1,2-dihydroxyethyl)dihydrofuran-2(3H)-one 
• 1311946-16-3 (4R,5R)-4-(benzyloxy)-5-((1S,2S,3R)-3-(tert-butyldimethylsilyloxy)-1,2-dihydroxy-3-phenylpropyl)dihydrofuran-2(3H)-one 
• 1311946-14-1 (4R,5R)-4-(benzyloxy)-5-((S,E)-3-(tert-butyldimethyl-silyloxy)-3-phenylprop-1-enyl)dihydrofuran-2(3H)-one 
• 1311946-12-9 (4R,5R)-4-(benzyloxy)-5-((S,E)-3-hydroxy-3-phenylprop-1-enyl)dihydrofuran-2(3H)-one 
• 1311946-04-9 (4R,5S)-4-(benzyloxy)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)dihydrofuran-2(3H)-one 

Downstream Products

• 144015-82-7 (–)-goniofufurone 
• 136778-39-7 (+)-goniofufurone 

Relevant academic research and scientific papers

A concise synthesis of (+)-goniofufurone, (+)-7-epi-goniofufurone, (+)-crassalactones B and C

The concise and efficient synthesis of (+)-goniofufurone, (+)-7-epi-goniofufurone, (+)-crassalactones B and C were achieved in 6 to 7 steps from the known D-glucono-δ-lactone derivative 9. An acid-mediated cascade cyclization was employed to construct the

Stereoselective total syntheses of (+)-exo- and (-)-exo-brevicomins, (+)-endo- and (-)-endo-brevicomins, (+)- and (-)-cardiobutanolides, (+)-goniofufurone

Stereoselective total syntheses of aggregation pheromones (+)-exo-brevicomin (9a), (-)-exo-brevicomin (9b), (+)-endo-brevicomin (9c), (-)-endo-brevicomin (9d) and styryllactones (+)-cardiobutanolide (14a), (-)-cardiobutanolide (14b), and (+)-goniofufurone

Stereoselective total synthesis of bioactive styryllactones (+)-goniofufurone, (+)7-epi-goniofufurone, (+)-goniopypyrone, (+)-goniotriol, (+)-altholactone, and (-)etharvensin

(Chemical Equation Presented) Stereoselective total synthesis of biologically active styryllactones 7-epi-goniofufurone, goniofufurone, goniopypyrone, goniotriol, altholactone, and etharvensin was achieved in high overall yields from a common intermediate

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

Stereocontrolled syntheses of (-)-goniofufurone and (-)-8-epi-goniofufurone

The absolute configurations of natural goniofufurone and 8-epi-goniofufurone are shown to be 2 and 4 respectively by unambiguous syntheses of their enantiomers 1 and 3 from D-glycero-D-gulo-heptono-γ-lactone 7 involving an intramolec