Wang and Co-workers

D. I. C. Wang and co-workers. Fermentation andEn me Technology, Wiley-Interscience, New York, 1979. 

The anion electronic effect in a recent analysis of the inhibition effect of bisulfate and comparison with the effect of OH adsorption (Pt-OH formation), Wang and co-workers found that the electronic effect must also be operative [Wang et al., 2004]. 

To further substautiate these insights for the ORR mechanism, Wang and co-workers analyzed the four-electron ORR in acidic media using an intrinsic kinetic equation with the free energies of activation and adsorption as the kinetic parameters [Wang JX et al., 2007]. The kinetic model consisted of four essential elementary reactions ... 

In addition to their work with solvent free systems, Wang and co-workers reported a water mediated Friedlander quinoline synthesis using hydrochloric acid and conventional heating to synthesize a variety of substituted quinolines in high yields <06TL1059>. 

The nucleophilic attack on an acceptor-substituted allene can also take place at the acceptor itself, especially in the case of carbonyl groups of aldehydes, ketones or esters. Allenic esters are reduced to the corresponding primary alcohols by means of diisobutylaluminum hydride [18] and the synthesis of a vinylallene (allenene) by Peterson olefination of an allenyl ketone has also been reported [172]. The nucleophilic attack of allenylboranes 189 on butadienals 188 was investigated intensively by Wang and co-workers (Scheme 7.31) [184, 203, 248, 249]. The stereochemistry of the obtained secondary alcohol 190 depends on the substitution pattern. Fortunately, the synthesis of the desired Z-configured hepta-l,2,4-trien-6-ynes 191 is possible both by syn-elimination with the help of potassium hydride and by anti-elimination induced by sulfuric acid. Analogous allylboranes instead of the allenes 189 can be reacted also with the aldehydes 188 [250]. 

Watercore in durian is usually associated with a bitter taste and unacceptable fruit quality so the ability of MRI to detect this condition is significant. The watercore disorder shows up as a bright region of increased free water near the central core of the fruit " not a dissimilar observation to that of Wang and co-workers with watercore in apples. 

In 2000 and 2001, fuel-cell models were produced by the dozens. These models were typically more complex and focused on such effects as two-phase flow ° where liquid-water transport was incorporated. The work of Wang and co-workers was at the forefront of those models treating two-phase flow comprehensively. The liquid-water flow was shown to be important in describing the overall transport in fuel cells. Other models in this time frame focused on multidimensional, transient, and more microscopic effects.The microscopic effects again focused on using an agglomerate approach in the fuel cell as well as how to model the membrane appropriately. 

Wang and co-workers [57,58] reported several Michael-type enantioselective additions with nitro-olefins. Under neat conditions, 1,3-dinitro compounds were generated in the 74 addition of nitroalkanes 75 to various P-substituted nitro-olefins (Scheme 15). Other Michael-type involving nitro-olefins reactions were illustrated using triazole donors 77 to offer good yields and high enantioselectivities (Scheme 16). 

Dicarbonyl donors are excellent Michael donors in asymmetric conjugate addition to a,p-nnsatnrated ketones. Wang and co-workers [79] applied chiral Cinchona-thiourea catalyst 131 to various carbon donors in the addition to aromatic enones. A diverse array of nucleophiles, mainly 1,3-dicarbonyls proceeded smoothly in the conjugate addition to a,p-unsaturated enone 132 (Scheme 29). 

Wang and co-workers reported a novel class of organocatalysts for the asymmetric Michael addition of 2,4-pentandiones to nitro-olefms [131]. A screen of catalyst types showed that the binaphthol-derived amine thiourea promoted the enantiose-lective addition in high yield and selectivity, unlike the cyclohexane-diamine catalysts and Cinchona alkaloids (Scheme 77, Table 5). 

Phenolic compounds have also been oxidatively polymerized to humic substances by clay minerals (29) and by the mineral fraction of a latasol (66). After a 10-day equilibration period, montmoril-lonite and illite clay minerals yielded 44 to 47% of the total added phenolic acids as humic substances whereas quartz gave only 9%. Samples of a latasol yielded over 63% of the total amount, from mixtures in varied proportion, of mono-, di- and trihydroxy phenolic compounds as humic substances (66). Extractions of the reaction products yielded humic, fulvic, and humin fractions that resembled soil natural fractions in color, in acid-base solubility, and in infrared absorption spectra. Wang and co-workers (67) further showed that the catalytic polymerization of catechol to humic substances was, enhanced by the presence of A1 oxide and increased with pH in the 5.0 to 7.0 range. Thus the normally very reactive products of Itgnin degradation can be linked into very stable humic acid polymers which will maintain a pool of potentially reactive phytotoxins in the soil. 

In 2007, Wang and co-workers published a protocol for an enantio- and diastereoselective domino Michael-aldol reaction using electron-rich and electron-deficient 2-mercaptobenzaldehydes and maleimides as substrates [223]. The conversion was described to proceed smoothly in the presence of bifunctional catalyst 12 (lmol% loading) in xylenes at 0°C reaction temperature producing the desired chiral succinimide-containing substituted thiochromanes 1-5 in high yields (83-96%), in synthetically useful ee values (74—94%), and diastereoselectivities (up to dr 20 1) in 7h reaction time (Scheme 6.71). 

Wang and co-workers developed a 121-catalyzed enantioselective Michael addition [149-152] of IH-benzotriazole to a variety of a,P-unsaturated ketones such as the model substrate 3-(4-chloro-phenyl)-l-phenyl-propenone affording the N-1 product 1 (Scheme 6.136) [291]. The evaluation of the reaction medium revealed... 

Further study by Katsuki, McMillen, Hashimoto, and Wang improved the enantioselectivity up to a moderately high level.Wang and co-workers further extended the asymmetric catalysis to the [2,3]-sigmatropic rearrangement of propargyl sulfonium ylide to give allenic products with up to 81% ee (Equation (18))." ... 

---