141116-46-3

Upstream product

• 69178-10-5 2-styryl-1,3-dithiane 
• 103-25-3 3-phenylpropanoic acid methyl ester 
• 96938-00-0 (R)-4-Phenyl-1-((R)-toluene-4-sulfinyl)-butan-2-ol 
• 141036-67-1 (R)-4-Phenyl-1-[2-((E)-styryl)-[1,3]dithian-2-yl]-butan-2-ol 
• 141036-65-9 (R)-4-Phenyl-1-p-tolylsulfanyl-butan-2-ol 
• 141036-66-0 (R)-(2-phenylethyl)oxirane 
• 96937-97-2 4-Phenyl-1-((R)-toluene-4-sulfinyl)-butan-2-one 
• 129529-65-3 (E)-1-((2S,3S)-3-Phenethyl-oxiranyl)-3-phenyl-prop-2-en-1-ol 
• 129529-66-4 (E)-1-((2R,3S)-3-Phenethyl-oxiranyl)-3-phenyl-propenone 

Relevant academic research and scientific papers

Asymmetric Synthesis of (-) (R) Yashabushiketol

(-)(R) Yashabushiketol was prepared from the epoxide 4 readily available in both configurations by reduction of β-ketosulfoxides.

An Expedient Synthesis of Natural Diarylheptanoids Using the Organoselenium-mediated Reduction of Epoxy Ketone

The total synthesis of diarylheptanoids isolated from the male flowers of Alnus sieboldiana, yashabushiketol, yashabushiketodiol A, yashabushiketodiol B, and yashabushitriol, has been achieved in short steps by employing the organoselenium-mediated reduct