73971-97-8

Upstream product

• 73972-04-0 N-[2-(7-Oxa-bicyclo[4.1.0]hepta-2,4-dien-1-yl)-ethyl]-benzamide 
• 2045-79-6 o-methoxy-2-phenylethylamine 
• 1181028-82-9 C₁₅H₁₆N₂O₂ 
• 98-88-4 benzoyl chloride 
• 73972-08-4 2-[2-(3,4-Dibromo-7-oxa-bicyclo[4.1.0]hept-1-yl)-ethyl]-isoindole-1,3-dione 
• 73972-02-8 2-[2-(7-Oxa-bicyclo[4.1.0]hepta-2,4-dien-1-yl)-ethyl]-isoindole-1,3-dione 
• 73971-98-9 2-(2-Cyclohexa-1,4-dienyl-ethyl)-isoindole-1,3-dione 
• 73972-00-6 2-[2-(7-Oxa-bicyclo[4.1.0]hept-3-en-1-yl)-ethyl]-isoindole-1,3-dione 
• 73971-96-7 1-(β-Aminoethyl)benzene Oxide 
• 21802-85-7 2-(cyclohexa-1,4-dien-1-yl)ethan-1-amine 
• 72251-65-1 2-[2-(3,4-Dibromo-7-oxa-bicyclo[4.1.0]hept-2-yl)-ethyl]-isoindole-1,3-dione 
• 74033-50-4 2-[2-(5,6-Dibromo-cyclohex-2-enyl)-ethyl]-isoindole-1,3-dione 
• 72251-58-2 2-[2-(7-Oxa-bicyclo[4.1.0]hepta-2,4-dien-2-yl)-ethyl]-isoindole-1,3-dione 
• 72251-61-7 2-(2-Cyclohexa-2,5-dienyl-ethyl)-isoindole-1,3-dione 

Downstream Products

• 1381861-10-4 C₁₆H₁₆N₂O₃ 

Relevant academic research and scientific papers

Improved protocol for indoline synthesis via palladium-catalyzed intramolecular C(sp2)-H amination

An efficient method has been developed for the synthesis of indoline compounds from picolinamide (PA)-protected β-arylethylamine substrates via palladium-catalyzed intramolecular amination of ortho-C(sp2)-H bonds. These reactions feature high efficiency, low catalyst loadings, mild operating conditions, and the use of inexpensive reagents.

Biogenesis of Epidithiadiketopiperazines. Synthesis of Three Isomeric (β-Aminoethyl)benzene Oxides

Three isomeric amine-substituted arene oxides have been synthesized to serve as models for the postulated involvement of amino acid derived arene oxides during the biosyntheses of various epidithiadiketopiperazines.No biogenetic-type reactivity was noted for the arene oxides.In all three cases aromatization rather than amine/epoxide cyclization was observed.The failure to duplicate the presumed in vivo reactivity of aminoarene oxides is discussed in terms of possible enzyme-mediated cyclizations in the natural systems.