877833-48-2

Upstream product

• 403805-83-4 methyl 4-(tert-butyldiphenylsilyloxy)-2-butynoate 
• 289893-42-1 methyl (Z)-4-t-butyldiphenylsilyloxy-3-methyl-2-butenoate 
• 877833-43-7 (S)-4-Benzyl-3-[(Z)-(2S,3R)-6-(tert-butyl-diphenyl-silanyloxy)-3-hydroxy-2,5-dimethyl-hex-4-enoyl]-oxazolidin-2-one 
• 877833-46-0 bromo-acetic acid 1-[2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-4-(tert-butyl-diphenyl-silanyloxy)-3-methyl-but-2-enyl ester 
• 877833-45-9 1-(tert-butyl-dimethyl-silanyloxy)-6-(tert-butyl-diphenyl-silanyloxy)-2,5-dimethyl-hex-4-en-3-ol 
• 877833-44-8 (Z)-(2R,3R)-6-(tert-Butyl-diphenyl-silanyloxy)-2,5-dimethyl-hex-4-ene-1,3-diol 
• 877833-53-9 4-(tert-butyl-diphenyl-silanyloxy)-3-methyl-but-2-en-1-ol 
• 877833-42-6 4-(tert-butyl-diphenyl-silanyloxy)-3-methyl-but-2-enal 
• 877833-47-1 Bromo-acetic acid (Z)-(R)-4-(tert-butyl-diphenyl-silanyloxy)-1-((R)-2-hydroxy-1-methyl-ethyl)-3-methyl-but-2-enyl ester 

Downstream Products

• 877833-52-8 (E)-4-{(2S,4S,5S,6R)-6-[(Z)-3-(tert-Butyl-diphenyl-silanyloxy)-2-methyl-propenyl]-5-methyl-4-triethylsilanyloxy-tetrahydro-pyran-2-yl}-but-2-enal 
• 877833-51-7 (2R,3S,4S,6S)-6-Allyl-2-[(Z)-3-(tert-butyl-diphenyl-silanyloxy)-2-methyl-propenyl]-3-methyl-4-triethylsilanyloxy-tetrahydro-pyran 
• 877833-50-6 (4S,5R,6R)-2-Allyl-6-[(Z)-3-(tert-butyl-diphenyl-silanyloxy)-2-methyl-propenyl]-5-methyl-tetrahydro-pyran-2,4-diol 

Relevant academic research and scientific papers

An efficient synthesis of the C1-C14 subunit of (-)-lasonolide A via a target oriented β-C-glycoside formation sequence

An efficient synthesis of the C1-C14 subunit resident in (-)-lasonolide A is reported herein. The key reaction features that were utilized include a Molander-Reformatsky SmI2 mediated intramolecular aldol reaction followed