76489-57-1

Upstream product

• 78-80-8 2-methylbut-1-en-3-yne 
• 281191-48-8 2-Acetoxy-1-iodo-4-methoxybenzene 
• 56518-59-3 3,5-dimethoxy-4-iodobenzaldehyde 
• 1218939-30-0 2-(4-iodo-3,5-dimethoxyphenyl)-6-methoxybenzofuran 
• 1218939-29-7 C₁₇H₁₅IO₄ 
• 1218939-28-6 2-((4-iodo-3,5-dimethoxyphenyl)ethynyl)-5-methoxyphenyl acetate 
• 1218939-27-5 5-ethynyl-2-iodo-1,3-dimethoxybenzene 
• 839705-26-9 gleinadiene 
• 76502-88-0 [(1S,2R,6R)-2-[2,6-Dimethoxy-4-(6-methoxy-benzofuran-2-yl)-phenyl]-6-(2,4-dimethoxy-phenyl)-4-methyl-cyclohex-3-enyl]-[2,4-dimethoxy-3-(3-methyl-but-2-enyl)-phenyl]-methanone 

Downstream Products

• 76489-58-2 trimethyldihydromoracin C 

Relevant academic research and scientific papers

Synthetic studies towards the mulberry Diels-Alder adducts: H-bond accelerated cycloadditions of chalcones

The methyl ether derivatives 2, 4 and 6 of the mulberry Diels-Alder adducts chalcomoracin (1) and mulberrofuran C (3) and kuwanon J (5) respectively have been synthesized by a thermal [4 + 2]-cycloaddition reaction between a chalcone and dehydroprenyl die

Mulberry Diels- Alder adducts: Synthesis of chalcomoracin and mulberrofuran C methyl ethers

(Figure Presented) The synthesis of each of the heptamethyl ethers of the mulberry Diels-Alder adducts chalcomoracin (1) and mulberrofuran J (2) is described. The key steps In each approach involved a biomimetic intermolecular [4+2]-cycloaddition between a dehydroprenylphenol diene derived from an Isoprenoid-substituted phenolic compound and an αβ-unsaturated alkene of a chalcone as the dienophlle. Critical to the success of the Diels-Alder reaction was the presence of the free phenol in the 2′-hydroxychalcone.

CHALCOMORACIN, A NATURAL DIELS-ALDER ADDUCT FROM DISEASED MULBERRY

The structure elucidation of a new phytoalexin, isolated from diseased mulberry leaves and designated as chalcomoracin, is described.The compound is regarded biogenetically as a Diels-Alder adduct of a chalcone, isolated newly from diseased mulberry shoot