143370-16-5

Upstream product

• 155781-68-3 (2R,3S)-3-Methyl-1-trityloxy-pent-4-en-2-ol 
• 155781-67-2 (2R,3R)-3-Methyl-1-trityloxy-pent-4-en-2-ol 
• 635727-09-2 (2R,3S)-1-Benzyloxy-3-methyl-pent-4-en-2-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 143347-62-0 (2R,3S)-3-Methylpent-4-en-1,2-diol 

Relevant academic research and scientific papers

First Example of Reversal of Normal Stereoselectivity in the Intramolecular Pauson-Khand Reaction

Stereoselectivity favoring exo substituent orientation in the intramolecular Pauson-Khand reaction of 3-methyl-4-hydroxy-1,6-heptenynes to form bicyclooctenones is affected by the relative stereochemistry at C3 and C4.Cycloaddition of one stereoiso