159266-71-4

Upstream product

• 159266-79-2 (4R,5S)-3-[(R)-2-((R)-2-Benzyloxy-1-hydroxy-ethyl)-6-(tert-butyl-dimethyl-silanyloxy)-hexanoyl]-4-methyl-5-phenyl-oxazolidin-2-one 
• 60656-87-3 benzyloxyacetoaldehyde 
• 100-39-0 benzyl bromide 
• 159266-70-3 (3S,4S)-4-((R)-1,2-Bis-benzyloxy-ethyl)-8-(tert-butyl-dimethyl-silanyloxy)-oct-1-en-3-ol 
• 159266-80-5 (R)-2-((R)-1,2-Bis-benzyloxy-ethyl)-6-(tert-butyl-dimethyl-silanyloxy)-hexanoic acid methoxy-methyl-amide 
• 159266-68-9 (R)-2-((R)-1,2-Bis-benzyloxy-ethyl)-6-(tert-butyl-dimethyl-silanyloxy)-hexanal 
• 159266-66-7 (R)-2-((R)-2-Benzyloxy-1-hydroxy-ethyl)-6-(tert-butyl-dimethyl-silanyloxy)-hexanoic acid methoxy-methyl-amide 

Downstream Products

• 159266-73-6 (5R,6R)-6-Benzyloxy-5-((R)-1,2-bis-benzyloxy-ethyl)-7,7-dimethoxy-heptanoic acid methyl ester 
• 159266-72-5 (5R,6R)-6-Benzyloxy-5-((R)-1,2-bis-benzyloxy-ethyl)-7,7-dimethoxy-heptan-1-ol 

Relevant academic research and scientific papers

SYNTHESIS OF TETRAHYDROTHIOPHENES VIA NUCLEOPHILIC ADDITION OF HARPP'S REAGENT TO CYCLIC CARBONATES: APPLICATION TOWARD THE SYNTHESIS OF BREYNOLIDE

A method for the conversion of a triol to a tetrahydrothiophene is described in which the key step involves ring cleavage of a cyclic carbonate with loss of carbon dioxide.