1551543-75-9

Upstream product

• 1551543-56-6 (3aR,4S,6S,6aR)-2,2-dimethyl-6-((Z)-prop-1-en-1-yl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl benzoate 
• 1551543-54-4 (3aR,4S,6R,6aR)-6-formyl-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl benzoate 
• 1551543-45-3 (3aR,4S,6S,6aR)-6-((R)-1,2-dihydroxyethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl benzoate 
• 1551601-15-0 (3aR,6S,6aR)-2,2-dimethyl-6-((Z)-prop-1-en-1-yl)dihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one 
• 1551543-36-2 (3S,4S,7R,8S,9R,10R,E)-8-((tert-butyldimethylsilyl)oxy)-10-methoxy-12-((4-methoxybenzyl)oxy)-3,5,7,9-tetramethyldodeca-1,5-dien-4-ol 
• 1551543-35-1 (4R,5R)-2,2-dimethyl-5-((R,E)-3-methylhexa-1,5-dien-1-yl)-1,3-dioxolane-4-carboxylic acid 
• 1551544-06-9 (3aR,4S,6S,6aR)-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl benzoate 
• 1551543-94-2 (4R,5S,6R,7R,E)-5-((tert-butyldimethylsilyl)oxy)-7-methoxy-9-((4-methoxybenzyl)oxy)-2,4,6-trimethylnon-2-enal 
• 1551543-91-9 (4R,5S,6R,7R,E)-5-((tert-butyldimethylsilyl)oxy)-7-methoxy-9-((4-methoxybenzyl)oxy)-2,4,6-trimethylnon-2-en-1-ol 
• 1551543-88-4 (2R,3S,4S,5R)-5-methoxy-7-((4-methoxybenzyl)oxy)-2,4-dimethylheptane-1,3-diol 
• 1551543-85-1 (2S,4R,5R)-1-((S)-4-benzyl-2-oxooxazolidin-3-yl)-5-methoxy-7-((4-methoxybenzyl)oxy)-2,4-dimethylheptane-1,3-dione 
• 1551543-73-7 (4R,5R)-(3S,4S,7R,8S,9R,10R,E)-8-((tert-butyldimethylsilyl)oxy)-10-methoxy-12-((4-methoxybenzyl)oxy)-3,5,7,9-tetramethyldodeca-1,5-dien-4-yl 2,2-dimethyl-5-((R,E)-3-methylhexa-1,5-dien-1-yl)-1,3-dioxolane-4-carboxylate 
• 1551543-71-5 (4R,5S,6S,7R,E)-methyl 5-((tert-butyldimethylsilyl)oxy)-7-methoxy-9-((4-methoxybenzyl)oxy)-2,4,6-trimethylnon-2-enoate 

Relevant academic research and scientific papers

A concise synthesis of carolacton

A synthesis of carolacton, a myxobacterial natural product that has profound effects on Streptococcus mutans biofilms, is reported. The synthesis proceeds via a longest linear sequence of 14 steps from an Evans β-ketoimide and enabled preliminary evaluations of the effects of late-stage intermediates on S. mutans biofilms. These studies suggest that further investigations into carolacton's structure-function relationships are warranted.