137104-40-6

Upstream product

• 137104-36-0 2-[Hydroxy-(4-isopropyl-phenyl)-methyl]-acrylic acid methyl ester 
• 122-03-2 (4-isopropylbenzaldehyde) 

Downstream Products

• 137104-57-5 methyl 2-<α-<(tert-butyl)amino>-4-isopropylbenzyl>prop-2-enoate 
• 213999-93-0 (E)-3-(4-Isopropyl-phenyl)-2-phenoxymethyl-acrylic acid methyl ester 
• 109754-23-6 3-(p-Isopropylbenzyliden)chroman-4-on 
• 213999-99-6 (E)-3-(4-Isopropyl-phenyl)-2-phenoxymethyl-acrylic acid 
• 137104-83-7 2-<α-<(tert-butyl)amino>-4-isopropylbenzyl>prop-2-enoic acid hydrochloride 
• 137104-87-1 1-(tert-butyl)-4-(4-isopropylphenyl)-3-methylideneazetidin-2-one 
• 1589493-38-8 (E)-methyl 2-((N-(2-formylphenyl)-4-methylphenylsulfonamido)-methyl)-3-(4-isopropylphenyl)acrylate 
• 1373930-78-9 methyl (E)-2-({2-[(E)-(hydroxyimino)methyl]phenoxy}methyl)-3-(4-isopropylphenyl)acrylate 

Relevant academic research and scientific papers

Baylis-Hillman chemistry: A novel synthesis of functionalized 1,4-pentadienes

A novel synthesis of functionalized 1,4-pentadienes via the reaction of acrylonitrile with allyl halides, derived from Baylis-Hillman adducts, in the presence of DABCO has been described, demonstrating for the first time the application of allyl halides a

Design, synthesis and evaluation of 3-arylidene azetidin-2-ones as potential antifungal agents against Alternaria solani Sorauer

A new concise and facile method was explored to synthesize a collection of new 3-arylidene azetidin-2-ones, which could be regarded as the derivatives of the hybrid scaffold of bioactive natural cinnamamide and heterocycle azetidi-2-one. The structures of

Multicomponent cascade assembly for quinolinopyranpyrazole architectures

A highly efficient, multicomponent protocol for the construction of functionalized quinolinopyranpyrazole scaffolds with high stereoselectivity has been developed through the application of a domino reaction. All the quinolinopyranpyrazoles were synthesiz

Multicomponent Cascade Assembly for Quinolinopyranpyrazole Architectures

A highly efficient, multicomponent protocol for the construction of functionalized quinolinopyranpyrazole scaffolds with high stereoselectivity has been developed through the application of a domino reaction. All the quinolinopyranpyrazoles were synthesiz

115. α-Methylidene-and α-alkylidene-β-lactams from nonproteinogenic amino acids

Treatment of methyl 2-(l-hydroxyalkyl)prop-2-enoates1 with conc. HBr solution afforded methyl (Z)-2-(bromomethyl)alk-2-enoates 2, which were transformed regioselectively into N-substituted methyl (E)-2-(aminomethyl)alk-2-enoates 3 (SN2 reaction