855127-50-3

Upstream product

• 855127-40-1 (2S,5S,6S)-6-[(R)-1-Benzyloxy-2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-5-methoxy-2-vinyl-tetrahydro-pyran-2-ol 
• 627-27-0 homoalylic alcohol 
• 100-39-0 benzyl bromide 
• 855127-46-7 (4S,5S,6R)-6-Benzyloxy-5,7-bis-(tert-butyl-dimethyl-silanyloxy)-hept-1-en-4-ol 
• 855127-48-9 [2-(tert-butyl-dimethyl-silanyloxy)-1-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-hex-5-enyloxymethyl]-benzene 
• 855127-42-3 (4S,5S,6R)-6-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-4-methoxy-heptane-1,5-diol 
• 855127-43-4 (2R,3R)-3-Benzyloxy-2,4-bis-(tert-butyl-dimethyl-silanyloxy)-butyraldehyde 
• 855127-49-0 (2R,3S,4S)-2-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxy)-4-methoxy-hept-6-en-3-ol 
• 855127-54-7 (2R,3S,4S)-2-Benzyloxy-4-methoxy-hept-6-ene-1,3-diol 
• 855127-45-6 (2R,3S)-2-Benzyloxy-pent-4-ene-1,3-diol 
• 855127-41-2 (5S,6S)-6-[(R)-1-Benzyloxy-2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-5-methoxy-tetrahydro-pyran-2-one 

Downstream Products

• 855127-39-8 [(R)-2-Benzyloxy-2-((2S,3S,6R)-3-methoxy-6-{(1R,2S)-1-[2-(4-methoxy-benzyloxy)-ethyl]-2-methyl-but-3-enyloxy}-6-vinyl-tetrahydro-pyran-2-yl)-ethoxy]-tert-butyl-diphenyl-silane 

Relevant academic research and scientific papers

A ketal-tethered RCM strategy toward the synthesis of spiroketal related natural products

An unconventional approach to construct spiroketals and spiroaminals via ring-closing metathesis [RCM] of cyclic ketals and aminals, respectively, is described here. This method possesses a good generality with no loss of stereochemical integrity at the s

Synthesis of the C11-C23 fragment of spirastrellolide A. A ketal-tethered RCM approach to the construction of spiroketals

(Chemical Equation Presented) The synthesis of the C11-C23 fragment in spirastrellolide A is described here featuring a ketal-tethered RCM as an alternative approach to the construction of spiroketals.