192884-89-2

Upstream product

• 14371-10-9 (E)-3-phenylpropenal 
• 1515-78-2 buta-1,3-dien-1-ylbenzene 
• 762-42-5 dimethyl acetylenedicarboxylate 
• 16939-57-4 (E)-buta-1,3-dienylbenzene 

Downstream Products

• 6221-93-8 1-dodecyl propionate 
• 50402-81-8 biphenyl-2,3-dicarboxylic acid dimethyl ester 
• 192884-95-0 4-Phenyl-4,7-dihydro-3H-isobenzofuran-1-one 
• 192884-96-1 7-Phenyl-4,5,6,7-tetrahydro-3H-isobenzofuran-1-one 
• 192884-94-9 7-Phenyl-4,7-dihydro-3H-isobenzofuran-1-one 
• 192884-91-6 4-phenyl-1,3,4,7-tetrahydroisobenzofuran-1,3-dione 

Relevant academic research and scientific papers

METHOD FOR PRODUCING AROMATIC COMPOUND USING HETEROGENEOUS NOBLE METAL CATALYST

PROBLEM TO BE SOLVED: To provide a technique for synthesizing aromatic compound such as indole by dehydrogenation reaction that is low in manufacturing cost, and a green technique that is low in environmental impact. SOLUTION: Provided is a method for pro

Highly-functionalized arene synthesis based on palladium on carbon-catalyzed aqueous dehydrogenation of cyclohexadienes and cyclohexenes

Transition metal-catalyzed dehydrogenation is a clean oxidation method requiring no additional oxidants. We have accomplished a heterogeneous Pd/C-catalyzed aqueous dehydrogenation of 1,4-cyclohexadienes and cyclohexenes to give the corresponding highly-functionalized arenes. Furthermore, various arenes could be efficiently constructed in a one-pot manner via a Diels-Alder reaction and the following dehydrogenation.

Furan-2(3H)- and -2(5H)-ones. Part 7. Photochemical behaviour of tetrahydro- and hexahydro-isobenzofuran-1-one systems: A mechanistic and exploratory study

The photoreactivity of two variations of the di-π-rnethane system involving the tetrahydro- and hexahydro-isobenzofuran structures 10 and 11 have been examined and compared with those of β-apolignans 1. The former, 9-phenyl-1,3,4,5,6,7,8,9-octahydronaphtho[2,3-c]furan-1-one 10a and 7-phenyl-1,3,4,7-tetrahydroisobenzofuran-1-one 10b, gave primarily the di-π-methane rearrangement products 18a and 18b, respectively, while the hexahydro substrate, 7-phenyl-1,3,4,5,6,7-hexahydroisobenzofuran-1-one 11, afforded mainly the photoreduced products 21-24. This difference in chemoselectivity is explained in terms of the variant configuration of the phenyl group, an axially orientated one migrating most effectively. A new pathway for the reaction leading to the cyclopropano product 18a or 18b, by way of another cyclopropano derivative 19a or 19b, respectively, is described.