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The role of Mo=O is most likely limited to being an H acceptor from isopropyl to form propene under ammoxidation conditions.
Cellulose whiskers resulting from the acid hydrolysis of tunicin were subjected to partial silylation by the addition in toluene of a series of alkyldimethylchlorosilanes, with alkyl moieties ranging from isopropyl to n-butyl, n-octyl and n-dodecyl.
Solvate-I is obtained from isopropyl alchocol, acetone and water as anti-solvent is subjected to GCMS analysis to ascertain the type of solvent present in the lattice.
The band at 2877 cm−1 are assigned to the C H asymmetric and symmetric vibrations from isopropyl group.
The solutions were made from Isopropyl Alcohol (IPA) and distilled water in different proportions, whose refractive is found in Glover and Goulden (1963).
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By varying the crystallization temperature and level of supersaturation, three of the four polymorphs of carbamazepine (CBZ; 5H-dibenz [b,f]azepine-5-carboxamide) were crystallized from cumene (isopropyl benzene).
In the transition state, protonation of the oxygen atom occurs through neighbouring Brønsted hydroxyl groups from the surface of the support.[ 48– 50] Subsequently, hydrogen is abstracted from the isopropyl group and the ring is closed to form isopulegol (Scheme 6).
Several inhibitors were synthesized from an l-Val methyl amide P2 motif by appending hydrogen bonding moieties from either the isopropyl side-chain or from the methyl amide portion.
Bacto™ yeast extract and tryptone were purchased from BD (Becton, Dickinson and Company), glucose and NaCl were purchased from Merck, glycerol from Invitrogen, kanamycin from Sigma and IPTG (isopropyl β-D-1-thiogalactopyranoside) was purchased from Promega.
It was observed that both enantioselectivity and conversion increased with increase in alcoholic carbon chain length of alkyl ester from methyl to isopropyl acetate, whereas further increase in alcoholic chain length from C4 to C8 led to decrease in conversion and enantioselectivity of reaction.
From an isopropyl-myristate suspension, the decyl ester was the most effective enhancer (4.9±1.4), while Azone was inactive.
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