120342-08-7

Upstream product

• 34164-50-6 4-penten-1-ylmagnesium bromide 
• 54313-25-6 4-penten-1-yllithium 
• 120342-05-4 1-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-hept-6-en-2-ol 
• 120342-07-6 (1S,3S,5S)-3-hydroxymethyl-1-methyl-2,9-dioxabicyclo<3.3.1>nonane 
• 98-59-9 p-toluenesulfonyl chloride 
• 120342-05-4 (2S,4S)-1,2-O-isopropylidene-8-nonen-1,2,4-triol 
• 120342-06-5 (2S,4S)-8-nonen-1,2,4-triol 

Relevant academic research and scientific papers

Stereoselective Synthesis of (1R,3R,5S)-1,3-Dimethyl-2,9-dioxabicyclononane

(1R,3R,5S)-1,3-Dimethyl-2,9-dioxabicyclononane (1), a host-specific substance of ambrosia beetle, has been synthesized stereoselectively based on a highly syn-selective 1,3-asymmetric reduction of the β-alkoxy ketone (5) using lithium aluminium hyd

STEREOSELECTIVE REDUCTION OF β-ALKOXY KETONES: A SYNTHESIS OF SYN-1,3-DIOLS

The diastereoselective reduction of acyclic β-alkoxy ketones with lithium aluminum hydride in the presence of lithium iodide has been studied and found to provide syn-1,3-diol derivatives with high diastereoselection.