952092-52-3

Upstream product

• 51694-22-5 ortho-nitrophenyl selenocyanate 
• 952092-51-2 (1R,4R,5S)-4-((1S,2S)-1-hydroxy-2-methoxy-4-(4-methoxybenzyloxy)butyl)-1-((S)-4-(4-methoxybenzyloxy)-3-methylbutanoyl)-7,7-dimethyl-2-oxabicyclo[3.2.0]heptan-3-one 
• 952092-48-7 (1R,4R,5S)-4-((1S,2S)-1,4-dihydroxy-2-methoxybutyl)-1-((S)-5-hydroxy-4-methylpent-1-en-2-yl)-7,7-dimethyl-2-oxabicyclo[3.2.0]heptan-3-one 
• 952092-49-8 (1R,4R,5S)-4-((1S,2S)-1,4-dihydroxy-2-methoxybutyl)-1-((S)-4-hydroxy-3-methylbutanoyl)-7,7-dimethyl-2-oxabicyclo[3.2.0]heptan-3-one 

Relevant academic research and scientific papers

An example of overriding cyanation during reaction of a primary alcohol with o-nitrophenyl selenocyanate

The first example of a nitrile as the end product of a Mitsunobu substitution involving o-nitrophenyl selenocyanate and tributylphosphine is reported. Neighboring group participation operates and leads favorably to competitive formation of a 2-cyanotetrah

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