868761-58-4

Upstream product

• 111828-49-0 (S,S)-(-)-N,N,N',N'-tetramethyl-2,2-dimethyl-1,3-dioxolane-trans-4,5-dicarboxamide 
• 868761-56-2 (4S,5S)-5-((S)-(tert-butyldimethylsilyloxy)(phenyl)methyl)-N,N,2,2-tetramethyl-1,3-dioxolane-4-carboxamide 
• 887927-67-5 (4S,5R)-5-((S)-hydroxy(phenyl)methyl)-N,N,2,2-tetramethyl-1,3-dioxolane-4-carboxamide 
• 868761-55-1 (4S,5S)-5-benzoyl-N,N,2,2-tetramethyl-1,3-dioxolane-4-carboxamide 
• 868761-57-3 1-((4S,5S)-5-((S)-(tert-butyldimethylsilyloxy)(phenyl)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)pent-4-en-1-one 

Downstream Products

• 887927-61-9 (⁽⁵⁾-((4S,5R)-S-((S)-1-(methoxymethoxy)pent-4-enyl)-2,2-dimethyl-1,3-dioxolan-4-yl)(phenyl)methoxy)(tert-butyl)dimethylsilane 
• 944353-00-8 ((S)-1-((4S,5R)-5-((S)-1-(benzyloxy)pent-4-enyl)-2,2-dimethyl-1,3-dioxolan-4-yl)(phenyl)methoxy)-tert-butyldimethylsilane 
• 887927-62-0 (S)-((4S,5R)-5-((S)-1-(methoxymethoxy)pent-4-enyl)-2,2-dimethyl-1,3-dioxolan-4-yl)(phenyl)methyl 4-methylbenzenesulfonate 
• 887927-64-2 (2S,3S,4S,5R)-2-(but-3-enyl)-3,4-bis-tert-butyldimethylsilyloxy-tetrahydro-5-phenylfuran 
• 887927-60-8 1-(S)-((4S,5S)-5-((S)-hydroxy(phenyl)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)pent-4-enyl 4-methylbenzenesulfonate 
• 887927-68-6 (S)-((4R,5R)-5-((S)-1-(methoxymethoxy)pent-4-enyl)-2,2-dimethyl-1,3-dioxolan-4-yl)(phenyl)methanol 
• 887927-65-3 (2R,3S,4S,5S)-2-(but-3-enyl)-tetrahydro-5-phenylfuran-3,4-diol 
• 887927-63-1 (2S,3S,4S,5R)-2-(but-3-enyl)-tetrahydro-5-phenylfuran-3,4-diol 
• 887927-69-7 1-(S)-((4S,5R)-5-((S)-tert-butyldimethylsilyloxy(phenyl)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)pent-4-enyl 4-methylbenzenesulfonate 

Relevant academic research and scientific papers

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

Stereoselective synthesis of (+)-goniothalesdiol

Stereoselective synthesis of antitumor tetrahydrofuran (+)-goniothalesdiol was achieved in high overall yield from (-)-D-tartaric acid. Key features include an FeCl3 mediated THF formation with very high selectivity. Synthesis of natural gonith