151130-64-2

Upstream product

• 88730-60-3 (Z)-6-(tetrahydro-2H-pyran-2-yloxy)hex-3-en-1-ol 
• 150-76-5 4-methoxy-phenol 

Downstream Products

• 151130-69-7 (Z)-6-(4-Methoxy-phenoxy)-hex-3-enylamine 
• 151130-70-0 Methanesulfonic acid (Z)-6-(4-methoxy-phenoxy)-hex-3-enyl ester 
• 151130-71-1 Benzyl-[(Z)-6-(4-methoxy-phenoxy)-hex-3-enyl]-amine 
• 151130-68-6 2-[(Z)-6-(4-Methoxy-phenoxy)-hex-3-enyl]-isoindole-1,3-dione 
• 151130-67-5 N-[(Z)-6-(4-Methoxy-phenoxy)-hex-3-enyl]-4-methyl-benzenesulfonamide 
• 151130-74-4 1-Benzyl-aziridine-2-carboxylic acid [(Z)-6-(4-methoxy-phenoxy)-hex-3-enyl]-amide 
• 151130-78-8 1-Benzyl-aziridine-2-carboxylic acid benzyl-[(Z)-6-(4-methoxy-phenoxy)-hex-3-enyl]-amide 
• 151130-66-4 C₂₅H₃₃NO₆S 
• 151130-72-2 N-(1-Benzyl-aziridine-2-carbonyl)-N-[(Z)-6-(4-methoxy-phenoxy)-hex-3-enyl]-4-methyl-benzenesulfonamide 
• 151130-65-3 (Z)-6-(4-Methoxy-phenoxy)-hex-3-en-1-ol 

Relevant academic research and scientific papers

Development of a Strategy for Synthesis of the Unusual Marine Alkaloid Sarain A

An 11-step approach to tricyclic compound 42, which contains the alkaloidal nucleus of the marine natural product sarain A (1), has been developed.Pivotal steps in the construction of 42 include stereospecific intramolecular dipolar -cycloaddition