227186-15-4

Upstream product

• 3344-77-2 12-bromododecanol 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 227186-06-3 13-(tert-Butyl-diphenyl-silanyloxy)-1-[(2R,5R)-5-((R)-1-methoxymethoxy-tridecyl)-tetrahydro-furan-2-yl]-tridecan-1-ol 
• 1260225-80-6 tert-butyldiphenyl(12-(phenylsulfonyl)dodecyloxy)silane 
• 1391985-77-5 14-(tert-butyldiphenylsilyloxy)-N-methoxy-N-methyl-2-(prop-1-en-2-yl)tetradecanamide 
• 1391985-69-5 tert-butyl(12-iodododecyloxy)diphenylsilane 
• 934737-68-5 (2R,15Z)-2-(benzyloxy)-N-((1S,2S,3R,4R,5Z)-2,3,4-tris(benzyloxy)-1-{[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)oxy]methyl}heptadec-5-en-1-yl)tetracos-15-enamide 
• 934737-67-4 (2R,15Z)-2-(benzyloxy)-N-[(1S,2S,3R,4R,5Z)-2,3,4-tris(benzyloxy)-1-(hydroxymethyl)heptadec-5-en-1-yl]tetracos-15-enamide 
• 934737-58-3 (2R,15E)-2-(benzyloxy)tetracos-15-enoic acid 
• 934737-66-3 (2R,15Z)-2-(benzyloxy)tetracos-15-enal 
• 934737-64-1 (2R,15Z)-2-(benzyloxy)tetracos-15-en-1-ol 
• 934737-65-2 (4R)-4-[(13Z)-docos-13-en-1-yl]-2-phenyl-1,3-dioxolane 
• 934737-61-8 (tert-butyl)({13-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]tridecyl}oxy)diphenylsilane 
• 934737-60-7 (tert-butyl)({(12Z)-13-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]tridec-12-en-1-yl}oxy)diphenylsilane 
• 1260225-98-6 tert-butyldiphenyl((17Z,20Z,23Z,26Z)-12-(phenylsulfonyl)dotriaconta-17,20,23,26-tetraenyloxy)silane 
• 1260226-00-3 (17Z,20Z,23Z,26Z)-12-(phenylsulfonyl)dotriaconta-17,20,23,26-tetraen-1-ol 

Relevant academic research and scientific papers

Total synthesis of a natural cerebroside from euphorbiaceae

The regioselective total synthesis of the natural cerebroside (2R,15Z)-N-{(1S,2S,3R,4R,5Z)-1-[(β-D-glucopyranosyloxy)methyl]-2,3, 4-trihydroxyheptadec-5-en-l-yl)-2-hydroxytetracos-15-enamide (2), originally isolated from Euphorbiaceae, is reported in full

Efficient macrocyclization by a novel oxy-oxonia-cope reaction: Synthesis and olfactory properties of new macrocyclic musks

Musk made to odor: A new oxy-oxonia-Cope macrocyclization to (3Z)-configured cycloalk-3-en-1-yl formates is reported, which is useful in the synthesis of unsaturated and saturated macrocyclic ketones (see scheme). The synthesized structures provide new insight into the structure-odor correlation of musks, making it likely for macrocyclic and linear alicyclic musks to address the same olfactory receptors.

Process for the Synthesis of Long-Chain Fatty Acids

This invention relates to processes for preparing long-chain fatty acids of Formula I: and salts thereof, as well as intermediates for the processes, wherein L1 and L2 are described herein.

Chemical synthesis of deuterium-labeled and unlabeled very long chain polyunsaturated fatty acids

First syntheses of a deuterium-labeled very long C34-containing polyunsaturated fatty acid, 34:5n5, and three other unlabeled very long chain C30-32 containing polyunsaturated fatty acids are reported. These syntheses were achieved by coupling chemically