952092-72-7

Upstream product

• 952092-32-9 C₁₇H₂₀O₄ 
• 952092-30-7 (1S,5R,6S,7S)-7-benzyloxy-8,8-dimethyl-5-vinyl-2-oxabicyclo[4.2.0]octan-3-one 
• 952092-33-0 (1S,6S,7S)-7-benzyloxy-8,8-dimethyl-2-oxabicyclo[4.2.0]oct-4-en-3-one 
• 952101-24-5 acrylic acid (1S,3S,4R)-3-benzyloxy-2,2-dimethyl-4-vinylcyclobutyl ester 
• 895532-66-8 (1S,3S,4R)-3-benzyloxy-2,2-dimethyl-4-vinylcyclobutanol 

Downstream Products

• 952092-36-3 (1S,5S,6S,7S)-7-benzyloxy-5-(methoxymethoxymethyl)-8,8-dimethyl-2-oxabicyclo[4.2.0]octan-3-one 
• 952101-35-8 thiocarbonic acid [(1S,5S,6S,7S)-7-hydroxy-5-(methoxymethoxymethyl)-8,8-dimethyl-3-oxo-2-oxabicyclo[4.2.0]oct-7-yl] ester p-tolyl ester 

Relevant academic research and scientific papers

Pestalotiopsin A. Enantioselective construction of potential building blocks derived from antipodal cyclobutanol intermediates

(Chemical Equation Presented) D-Glyceraldehyde acetonide has been used as the starting point for accessing the enantiomeric cyclobutanols 11 in optically pure condition. The dextrorotatory enantiomer has been transformed in five steps into the [3.2.0] bic

Pestalotiopsin A. Side chain installation and exhaustive probing of olefin metathesis as a possible tool for elaborating the cyclononene ring

(Chemical Equation Presented) A program directed toward an asymmetric synthesis of pestalotiopsin A is described. The routing begins with the dextrorotatory cyclobutanol 37, which is combined with the enantiomerically defined building blocks ent-15 and 16