53392-23-7

Upstream product

• 35693-15-3 p-methoxyphenylmethanol-1,1-d2 
• 121-98-2 methyl 4-methoxybenzoate 

Downstream Products

• 14202-49-4 p-methoxytoluene-α,α,α-d3 
• 131088-93-2 4-(2H₂)methylanisole 
• 1393345-83-9 C₁₇H₁₇⁽²⁾H₂NO₄S 
• 1378478-16-0 C₃₀H₃₂⁽²⁾H₂N₂O₆S 

Relevant academic research and scientific papers

Structural Optimizations of Thieno[3,2-b]pyrrole Derivatives for the Development of Metabolically Stable Inhibitors of Chikungunya Virus

Chikungunya virus (CHIKV) is a re-emerging vector-borne alphavirus, and there is no approved effective antiviral treatment currently available for CHIKV. We previously reported the discovery of thieno[3,2-b]pyrrole 1b that displayed good antiviral activit

A new procedure for deconvolution of inter-/intramolecular intrinsic primary and α-secondary deuterium isotope effects from enzyme steady-state kinetic data

The A2B2 flavocytochrome p-cresol methylhydroxylase (PCMH) from Pseudomonas putida oxidizes 4-methylphenol (p-cresol) to 4-hydroxybenzyl alcohol in a process requiring scission of an α-C-H bond with concomitant reduction of covalently bound FAD in each A subunit. Values of k(cat)/K were determined from steady-state kinetic data for the reactions of PCMH with the following substrates: 4-methylphenol, 4-(2H1)methylphenol, 4- (2H2)methylphenol, and 4-(2H3)methylphenol. A procedure was devised to extract the intrinsic primary deuterium and intrinsic α-secondary deuterium kinetic isotope effects from these values of k(cat)/K. The primary effect, P, is 6.71 ± 0.08, and the secondary effect, S, is 1,013 ± 0.014. The magnitudes of these effects are discussed in terms of an early or late transition state, hydrogen tunneling, coupled motion between the leaving and remaining hydrogens of the methyl group, and a H- expulsion mechanism versus a substrate radical mechanism versus a covalent substrate-FAD intermediate mechanism. The reaction of 4-ethylphenol with PCMH produces 4-vinylphenol and (-)-S-1-(4-hydroxyphenyl)ethanol (~100% enantomeric excess). The evidence indicates that these are formed from a common intermediate, presumably a p- quinone methide. From the partition ratios for the formation of the alcohol and 4-vinylphenol from 4-ethylphenol, 4-(1',1'-2H2)ethylphenol, and 4- (2',2',2'-2H3)ethylphenol, the primary isotope effect for conversion of the p-quinone (2',2',2'2H3)methide to 4-(2',2'-2H2)vinylphenol was estimated to be about 2, and the α-secondary isotope effect for conversion of p- quinone (1'-2H1)methide to 1-(4-hydroxyphenyl)-(1'-2H1)ethanol was found to be inverse (=0.83), as expected for sp2 to sp3 hybridization change at the α-carbon. Values of k(cat)/K were determined for 4-ethylphenol, R,S- (±)-4-(1'-2H1)ethylphenol (abbreviated R,S-D), S-(-)-4-(1'- 2H1)ethylphenol (S-D), R-(+)- 4-(1'-2H1)ethylphenol (R-D), and 4- (1',1',2H2)ethylphenol (D2). The (D2)(k(cat)/K) value was found to be 5.1- 6.1, the same as determined in an earlier study. Unexpectedly, the values for (R,S-D)(k(cat)/K), (S-D)(k(cat)/K), and (R-D)(k(cat)/K) were all about the same (~1.7), indicating that there is nearly an equal probability for pro-R or pro-S C-H bond scission. An apparent flux ratio for the pro-S path/pro-R path was estimated to be 0.78 ± 0.02. The same procedure devised to determine values for P and S for 4-methylphenol was used to determine these values for the 4-ethylphenol reaction (commitment to catalysis = 0); P = 5.98 ± 0.12 and S = 0.967 ±0.021. These values are essentially the same as those determined for 4-methylphenol. Thus, the chemical mechanisms for both substrates are assumed to be similar.

Side Chain Hydroxylation of Aromatic Compounds by Fungi. Part 4. Influence of the para Substituent on Kinetic Isotope Effects During Benzylic Hydroxylation by Mortierella isabellina

The benzylic hydroxylation of a series of para-substituted toluenes by the fungus Mortierella isabellina has been studied by using CD3, CHD2, and CH2D methyl labelled substrates.Inter- and intramolecular primary and secondary deuterium kinetic isotope effect ratios have been determined: the intermolecular primary effects are maximal with strongly electron-withdrawing para substituents (R = CN and CF3), while the intramolecular primary effects are minimal for R = H but increase in instances where R is electron donating or withdrawing.These results are interpreted in terms of a dependence of the hydroxylation mechanism on the nature of the para substituent.

Isotope effects in nucleophilic substitution reactions. IV. The effect of changing a substituent at the α carbon on the structure os SN2 transition states

Kinetic studies, secondary α-deuterium kinetic isotope effects, primary chlorine kinetic isotope effects (1), Hammett ρ values determined by changing the substituent in the nucleophile, and activation parameters have been used to determine the detailed (relative) structures of the transition states for the S2 reactions between para-substituted benzyl chlorides and thiophenoxide ion.A rationale for the U-shaped Hammett ρ plots observed when para-substituted benzyl compounds react with negatively charged nucleophiles is also presented.