147033-16-7

Upstream product

• 147033-15-6 (2E,4S,5R,6S,7R,8R,10R)-10-<(2R,4R,5S,6S)-6-<(2R,3S)-2-ethyl-3-methyl-1,4-dioxaspiro<4.4>nonan-3-yl>-4-<2-(4-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl>>-5,8-dihydroxy-7-(4-methoxybenzyloxy)-4,6,8-trimethyl-2-undecene 
• 160625-13-8 (2S)-2-<(2R,4R,5S,6R)-6-<(2R,3S)-2-ethyl-3-methyl-1,4-dioxaspiro<4.4>nonan-3-yl>-2-<2-(4-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl>>propanal 
• 147033-10-1 (2R,3S)-2-ethyl-3-<<(2R,4S,3S,5S,6R)-2-(4-methoxyphenyl)-5-methyl-4-<(1R,2E)-1-methyl-2-butenyl>>-1,3-dioxan-6-yl>-3-methyl-1,4-dioxaspiro<4.4>nonane 
• 147033-11-2 (2E,4R)-4-<(2R,4S,5S,6R)-6-<(2R,3S)-2-ethyl-3-methyl-1,4-dioxaspiro<4.4>nonan-3-yl>-4-<2-(4-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl>>-2-methyl-2-penten-1-ol 
• 160429-72-1 ethyl (2E,4R)-4-<(2R,4S,5S,6R)-6-<(2R,3S)-2-ethyl-3-methyl-1,4-dioxaspiro<4.4>nonan-3-yl>-4-<2-(4-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl>>-2-methyl-2-pentenoate 
• 160429-76-5 (2E,4S,5R,6R,8R)-8-<(2R,4R,5S,6S)-6-<(2R,3S)-2-ethyl-3-methyl-1,4-dioxaspiro<4.4>nonan-3-yl>-4-<2-(4-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl>>-6-hydroxy-5-(4-methoxybenzyloxy)-4,6-dimethyl-2-nonene 
• 824-94-2 p-methoxybenzyl chloride 
• 120788-81-0 (2R,3R)-3-ethyl-2-methyl-1,4-dioxaspiro<4.4>nonane-2-carbaldehyde 
• 120788-82-1 (2R,3S)-2-ethyl-3-<(1R,2S,3E)-1-hydroxy-2-methyl-3-pentenyl>-3-methyl-1,4-dioxaspiro<4.4>nonane 
• 147033-08-7 (2R,3S)-2-ethyl-3-<(1R,2R)-1-(4-methoxybenzyloxy)-2-methyl-3-oxopropyl>-3-methyl-1,4-dioxaspiro<4.4>nonane 
• 161912-57-8 (2R,3S)-2-ethyl-3-<(1R,2S,3E)-1-(4-methoxybenzyloxy)-2-methyl-3-pentenyl>-3-methyl-1,4-dioxaspiro<4.4>nonane 
• 147033-09-8 (2R,3S)-2-ethyl-3-<(1R,2S,3S,4R,5E)-3-hydroxy-1-(4-methoxybenzyloxy)-2,4-dimethyl-5-heptenyl>-3-methyl-1,4-dioxaspiro<4.4>nonane 
• 160497-72-3 (E)-(1R,2S)-1-((2R,3S)-3-{(S)-1-[(2R,4S,5S,6R)-6-((2R,3R)-3-Ethyl-2-methyl-1,4-dioxa-spiro[4.4]non-2-yl)-2-(4-methoxy-phenyl)-5-methyl-[1,3]dioxan-4-yl]-ethyl}-2-methyl-oxiranyl)-2-methyl-pent-3-en-1-ol 

Downstream Products

• 130532-31-9 (9S)-3,5,9,11-bis(4-methoxybenzylidene)dihydro-erythronolide A 

Relevant academic research and scientific papers

Stereoselective Synthesis of Alcohols, XLVIII - Linear Synthesis of (9S)-Dihydro-erythronolide A

Starting from building block 3 comprising the C-7 to C-15 segment of erythronolide A, a linear synthesis of erythronolide A has been achieved.Key steps were a Sharpless-epoxidation to set up the stereocenter at C-6, and two stereoselective allylboration r