1289513-17-2

Upstream product

• 1063693-99-1 (2S,3R,5R)-5-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-3-hydroxy-5-methyl-tetrahydro-furan-2-carboxylic acid methyl ester 
• 1289513-04-7 (2S,3R,5R)-methyl 3-[(tert-butyldimethylsilyl)oxy]-5-{(S)-2-[(tert-butyldimethylsilyl)oxy]-1-hydroxyethyl}-5-methyltetrahydrofuran-2-carboxylate 
• 1289513-05-8 (2S,3R,5R)-methyl 3-[(tert-butyldimethylsilyl)oxy]-5-{(S)-2-[(tert-butyldimethylsilyl)oxy]-1-[(4-methoxybenzyl)oxy]ethyl}-5-methyltetrahydrofuran-2-carboxylate 
• 1289513-06-9 (2S,3R,5R)-3-[(tert-butyldimethylsilyl)oxy]-5-{(S)-2-[(tert-butyldimethylsilyl)oxy]-1-[(4-methoxybenzyl)oxy]ethyl}-5-methyltetrahydrofuran-2-carbaldehyde 
• 1289513-11-6 (R)-6-[(benzyloxy)methyl]-1-((2R,3R,5R)-3-[(tert-butyldimethylsilyl)oxy]-5-{(S)-2-[(tert-butyldimethylsilyl)oxy]-1-[(4-methoxybenzyl)oxy]ethyl}-5-methyltetrahydrofuran-2-yl)-1-hydroxyhept-6-en-3-one 
• 1289513-15-0 (1R,3S)-6-[(benzyloxy)methyl]-1-((2R,3R,5R)-3-[(tert-butyldimethylsilyl)oxy]-5-{(S)-2-[(tert-butyldimethylsilyl)oxy]-1-[(4-methoxybenzyl)oxy]ethyl}-5-methyltetrahydrofuran-2-yl)-3-methylhept-6-ene-1,3-diol 
• 69739-34-0 t-butyldimethylsiyl triflate 

Downstream Products

• 1289513-19-4 (S)-2-((2R,4R,5R)-5-{(1S,3R,5S)-1-[(benzyloxy)methyl]-5-methyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-4-[(tert-butyldimethylsilyl)oxy]-2-methyltetrahydrofuran-2-yl)-2-[(4-methoxybenzyl)oxy]ethanol 
• 1289513-22-9 (R)-2-((2R,4R,5R)-5-{(1S,3R,5S)-1-[(benzyloxy)methyl]-5-methyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-4-[(tert-butyldimethylsilyl)oxy]-2-methyltetrahydrofuran-2-yl)-2-[(4-methoxybenzyl)oxy]acetaldehyde 
• 1289513-26-3 (1S,2R)-2-((2R,4R,5R)-5-{(1S,3R,5S)-1-[(benzyloxy)methyl]-5-methyl-2,8-dioxabicyclo[3.2.1]octan-3-yl}-4-[(tert-butyldimethylsilyl)oxy]-2-methyltetrahydrofuran-2-yl)-1-[(4-methoxybenzyl)oxy]but-3-en-2-ol 

Relevant academic research and scientific papers

Synthetic studies towards pectenotoxin-2: Synthesis of the nonanomeric 10-epi-ABCDE ring segment by kinetic spiroketalization

The synthesis of the nonanomeric 10-epi-ABCDE ring system of pectenotoxin-2 has been achieved by using a kinetic spiroketalization reaction. The synthesis of the spiroketalization precursor was achieved through a cross-metathesis/ hydrogenation sequence.