947409-45-2

Upstream product

• 947409-39-4 2-chloro-6-nitrophenyl acetylene 
• 119-61-9 benzophenone 
• 6361-22-4 2-chloro-6-nitrobenzaldehyde 
• 83-42-1 6-chloro-2-nitrotoluene 

Downstream Products

• 1353714-86-9 C₂₈H₂₁ClN₄O₃ 
• 1353714-85-8 C₂₈H₂₁ClN₄O₃ 

Relevant academic research and scientific papers

Diels-Alder approach to tetra-ortho-substituted biaryls employing propargylic tertiary alcohols as dienophiles

(Chemical Equation Presented) The efficient synthesis of a series of tetra-ortho-substituted biaryls is described utilizing a Diels-Alder reaction between propargylic tertiary alcohols and cyclic oxygenated dienes. The successful resolution of one of the

METHOD FOR MAKING BIARYL COMPOUNDS, COMPOUNDS MADE BY THE METHOD, AND METHOD FOR THEIR USE

Certain disclosed embodiments of the present invention concern a method for making biaryl compounds by combining a diene with a dienophile under reaction conditions that facilitate a Diels-Alder reaction. Certain embodiments are particularly directed to making a tetra-ortho-substituted biaryl compounds. The disclosed method may involve using novel dienes, dienophiles, or both. Similarly, certain of the biaryl compounds are novel compounds too. Additional disclosed embodiments concern a method for making useful compounds by first making a Diels-Alder adduct. The Diels-Alder adduct is then further modified or coupled to other compounds. The method can be used to make carbazoles, such as Siamenol. Disclosed biaryl compounds are useful for a number of applications, such as pharmacophores and organocatalysts.