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Journal articles on the topic 'Nitrobenzylic derivatives'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 February 2022

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1

Šolomek, Tomáš, Sébastien Mercier, Thomas Bally, and Christian G. Bochet. "Photolysis of ortho-nitrobenzylic derivatives: the importance of the leaving group." Photochemical & Photobiological Sciences 11, no. 3 (2012): 548. http://dx.doi.org/10.1039/c1pp05308f.

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2

Becker, R., W. Hoffmann, A. Knorr, W. Walther, and A. Lehmann. "Determination of zinc O,O?-dialkyl dithiophosphate lubricant additives via the corresponding methyl and p-nitrobenzylic ester derivatives using GC-MS, GC-NPD and HPLC-MS." Fresenius' Journal of Analytical Chemistry 357, no. 6 (1997): 688–94. http://dx.doi.org/10.1007/s002160050235.

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3

Liang, Dinghua, Xing Wu, Brian B. Hasinoff, David E. Herbert, and Geoffrey K. Tranmer. "Evaluation of Nitrobenzyl Derivatives of Camptothecin as Anti-Cancer Agents and Potential Hypoxia Targeting Prodrugs." Molecules 23, no. 8 (2018): 2041. http://dx.doi.org/10.3390/molecules23082041.

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As part of our initial efforts into developing a tumor-targeting therapy, C-10 substituted derivatives of a camptothecin analog (SN-38) have been synthesized (2-, 3- and 4-nitrobenzyl) for use as potential hypoxia-activated prodrugs and evaluated for their cytotoxicity, topoisomerase I inhibition and electrochemical (reductive) properties. All three derivatives were found to possess reduced toxicity towards human leukemia K562 cells compared to SN-38, validating a condition for prodrug action. Using an MTS assay, IC50’s were found to be 3.0, 25.9, 12.2 and 58.0 nM for SN-38, 2-nitro-, 3-nitro-

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4

Wan, Peter, S. Muralidharan, Iain McAuley та Christopher A. Babbage. "Photooxygenation of nitrobenzyl derivatives. Mechanisms of photogeneration and hydrolysis of α-hydroperoxy nitrobenzyl ethers". Canadian Journal of Chemistry 65, № 8 (1987): 1775–83. http://dx.doi.org/10.1139/v87-299.

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The photooxygenation of nitrobenzyl derivatives 1–10 has been studied in aqueous solution as a function of pH. For m-nitrobenzyl ethers 2–4 and 9, stable α-hydroperoxy ethers (11–13) are the primary photochemical products. Acid hydrolysis of 11–13 gives m-nitrobenzaldehyde and hydrogen peroxide. Quantum yields for photooxygenation are reported for a number of derivatives as a function of pH. Acid and base catalyses of photooxygenation are observed for several compounds. A mechanism involving photogenerated nitrobenzyl carbanion intermediates is proposed.

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5

Yan, Tay Karh, Asnuzilawati Asari, Siti Aishah Salleh, and Wahizatul Afzan Azmi. "Eugenol and Thymol Derivatives as Antifeedant Agents against Red Palm Weevil, Rhynchophorus ferrugineus (Coleoptera: Dryophthoridae) Larvae." Insects 12, no. 6 (2021): 551. http://dx.doi.org/10.3390/insects12060551.

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Coconut palms in Malaysia are infested by a destructive invasive pest, RPW since 2007, and the pest’s population is difficult to control. At present, RPW control management mainly relies on the use of monocrotophos, which is administered by the trunk injection method. However, this pesticide can negatively impact human health and the ecosystem. Plant EO that can be used as a bio-pesticide is highly recommended as an alternative to monocrotophos because of its target-specific and eco-friendly properties. The antifeedant activity of eight eugenol and thymol derivatives from clove and thyme EOs w

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6

Wan, Peter, and S. Muralidharan. "Photochemical retro-aldol type reactions of nitrobenzyl derivatives. Mechanistic variations in the elimination of nitrobenzyl carbanions from nitrobenzyl derivatives on photolysis." Canadian Journal of Chemistry 64, no. 9 (1986): 1949–51. http://dx.doi.org/10.1139/v86-321.

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The photochemical retro-aldol type reactions of several nitrobenzyl derivatives are reported. The reactions are observed only in aqueous solution with quantum efficiencies being pH dependent for several derivatives, consistent with the existence of several mechanistic pathways for reaction. The primary photochemical event is believed to involve the generation of a nitrobenzyl carbanion, which acts as a photolabile leaving group in these reactions, and the generation of an oxocarbocation (or oxocarbocation-derived) fragment.

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7

Morrison, James, Peter Wan, John ET Corrie та V. Ranjit Munasinghe. "Chemistry of photogenerated α-hydroxy-p-nitrobenzyl carbanions in aqueous solution: protonation vs. disproportionation". Canadian Journal of Chemistry 81, № 6 (2003): 586–97. http://dx.doi.org/10.1139/v03-045.

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The photochemistry of p-nitrobenzyl derivatives 610 has been studied in aqueous solution as a function of pH, using product analysis, UVvis spectrophotometry, and laser flash photolysis (LFP). The compounds were chosen with the aim of further exploring the propensity of these systems to give rise to α-hydroxy-p-nitrobenzyl carbanions on photolysis, and to study their mechanisms of subsequent reaction. α-Hydroxy-substituted carbanions are anions that cannot be readily formed using thermal routes but which are believed to have some interesting chemistry. Three methods were employed for photoge

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8

Prousek, Josef. "Preparation and alkylation reactions of 4-nitrobenzyl and 5-nitrofurfuryl sulfones." Collection of Czechoslovak Chemical Communications 53, no. 4 (1988): 851–56. http://dx.doi.org/10.1135/cccc19880851.

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Substitution reaction of 5-nitrofurfuryl bromide (I) with sodium thiophenoxide and 4-chlorothiophenoxide in dimethyl sulfoxide at 20 °C and oxidation with dimethyl sulfoxide in the reaction medium afforded 5-nitrofurfuryl phenyl sulfone (IVa) and 5-nitrofurfuryl 4-chlorophenyl sulfone (IVb), respectively. Similarly, 4-nitrobenzyl bromide reacted with sodium 4-chlorothiophenoxide to give 4-nitrobenzyl 4-chlorophenyl sulfone (VII) and with sodium phenylsulfinate to afford 4-nitrobenzyl phenyl sulfone (IX). The sulfide intermediates were not isolated. The sulfone IX was used as substrate in alkyl

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9

Xue, Yuan, Kai Ye, Xuebin Wang, et al. "Precise macroscopic supramolecular assembly of photopatterned hydrogels." Chemical Communications 57, no. 70 (2021): 8786–89. http://dx.doi.org/10.1039/d1cc03428f.

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Photoligation chemistry of o-nitrobenzyl derivatives is applied to photopattern amine-containing polyelectrolytes on the surface of hydrogels, so as to achieve precise macroscopic self-assembly by electrostatic interaction.

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10

Bujok, Robert, and Mieczysław Mąkosza. "Synthesis of Diarylacetylenes Bearing Electron-Withdrawing Groups via the Smiles Rearrangement." Synthesis 51, no. 16 (2019): 3109–16. http://dx.doi.org/10.1055/s-0037-1612423.

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Nitrobenzyl benzothiazol-2-yl sulfones and nitrobenzyl 1-phenyl-1H-tetrazol-5-yl sulfones react with chlorides of aromatic acids to form β-acyl derivatives. These products undergo the Smiles rearrangement resulting in the formation of the corresponding nitrophenyl arylacetylenes in 50–60% overall yields (approx. 75% per step). Sulfones bearing CF3 or CN groups instead of a NO2 substituent form mixtures of the acetylenes in moderate yields and benzyl aryl ketones in yields above 40%.

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11

Agbanyo, F. R., D. Vijayalakshmi, J. D. Craik, et al. "5′-S-(2-aminoethyl)-N6-(4-nitrobenzyl)-5′-thioadenosine (SAENTA), a novel ligand with high affinity for polypeptides associated with nucleoside transport. Partial purification of the nitrobenzylthioinosine-binding protein of pig erythrocytes by affinity chromatography." Biochemical Journal 270, no. 3 (1990): 605–14. http://dx.doi.org/10.1042/bj2700605.

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Derivatives of N6-(4-aminobenzyl)adenosine (substituted at the aminobenzyl group) and 5′-linked derivatives of N6-(4-nitrobenzyl)adenosine (NBAdo) were evaluated as inhibitors of site-specific binding of [3H]nitrobenzylthioinosine (NBMPR) to pig erythrocyte membranes. Potent inhibitors were SAENTA [5′-S-(2-aminoethyl)-N6-(4-nitrobenzyl)-5′-thioadenosine] and acetyl-SAENTA (the 2-acetamidoethyl derivative of SAENTA). SAENTA was coupled to derivatized agarose-gel beads (Affi-Gel 10) to form an affinity matrix for chromatographic purification of NBMPR-binding polypeptides, which in pig erythrocyt

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12

Amankavičienė, Virgine, Svajus J. Asadauskas, Jolanta Girnienė, and Algirdas Šačkus. "Synthesis of Functionalised Indoline Spiropyrans by Condensation of Indolo[2,1-b][1,3]Benzoxazines with Ortho-hydroxy-substituted Aromatic Aldehydes." Journal of Chemical Research 2005, no. 9 (2005): 580–82. http://dx.doi.org/10.3184/030823405774308817.

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Condensation of 5a,6-dihydro-5a,6,6-trimethyl-2-nitro-12H-indolo[2,1-b][1,3]benzoxazine derivatives with ortho-hydroxy-substituted aromatic aldehydes afforded 1′-(2-hydroxy-5-nitrobenzyl)spiro[1-benzopyran-2,2′-indoline].

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13

Schneider, Tobias, Joshua Martin, Patrick Durkin, Vladimir Kubyshkin, and Nediljko Budisa. "The Regioselective Synthesis of o-Nitrobenzyl DOPA Derivatives." Synthesis 49, no. 12 (2017): 2691–99. http://dx.doi.org/10.1055/s-0036-1588766.

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Photocaged DOPA derivatives may serve for non-invasive unmasking of the catechol fragment in biological systems. This would enable efficient control of the redox and metal-coordinating properties associated with the free catechol moiety, in particular, in biosynthetically produced adhesive proteins and synthetic peptides. Synthetic routes towards photocaged DOPA derivatives are reported herein. A new method for preparing para-alkylated DOPA starting from 3,4-dihydroxybenzaldehyde is described for the first time.

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14

Paul, Amrita, Avijit Jana, S. Karthik, Manoranjan Bera, Yanli Zhao, and N. D. Pradeep Singh. "Photoresponsive real time monitoring silicon quantum dots for regulated delivery of anticancer drugs." Journal of Materials Chemistry B 4, no. 3 (2016): 521–28. http://dx.doi.org/10.1039/c5tb02045j.

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Photoluminescent silicon quantum dots (SiQDs) decorated using o-nitrobenzyl (ONB) derivative as a phototrigger for real-time monitoring of chlorambucil (Cbl) based on Photoinduced Electron Transfer (PET).

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15

Wang, Chenxi, Yuan Liu, Chunyan Bao, et al. "Phototriggered labeling and crosslinking by 2-nitrobenzyl alcohol derivatives with amine selectivity." Chemical Communications 56, no. 15 (2020): 2264–67. http://dx.doi.org/10.1039/c9cc09449k.

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16

Zhai, Baoping, Wei Hu, Jinyu Sun, et al. "A two-photon fluorescent probe for nitroreductase imaging in living cells, tissues and zebrafish under hypoxia conditions." Analyst 142, no. 9 (2017): 1545–53. http://dx.doi.org/10.1039/c7an00058h.

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A two-photon fluorescent probe FNTR, constructed for nitroreductase by using a fluorine derivative as a TP fluorophore and a p-nitrobenzyl carbamate group as a recognition domain, was successfully applied to detect endogenous NTR in living cells, tissues and zebrafish.

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17

Górska, Agata, Lidia Chomicz, Justyna Żebrowska, et al. "Synthesis and Antimycobacterial and Antiprotozoal Activities of Some Novel Nitrobenzylated Heterocycles." Zeitschrift für Naturforschung B 61, no. 1 (2006): 101–7. http://dx.doi.org/10.1515/znb-2006-0120.

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A series of N-, S-, and O-mononitro- and dinitrobenzyl derivatives of heterocycles was synthesized by alkylation of heterocyclic bases with the respective nitrobenzyl chlorides. Of the newly synthesized compounds, dinitrobenzylsulfanyl derivatives of 1-methyl-2-mercaptoimidazole (2c) and of 5-nitro- and 5,6-dichloro-2-mercaptobenzimidazole (8b and 8c, and 8e and 8f, respectively) showed considerable antimycobacterial activity. On a molar basis, nine of the novel compounds showed also a considerably higher antiprotozoal efficacy than metronidazole that reduced T. hominis viability to 73.5% at 8

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18

Krutošíková, Alžbeta, and Mikuláš Hanes. "Substituted 4-Benzylfuro[3,2-b]pyrroles." Collection of Czechoslovak Chemical Communications 57, no. 7 (1992): 1487–94. http://dx.doi.org/10.1135/cccc19921487.

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Preparation of 4-benzylfuro[3,2-b]pyrroles is described and their reactions with selected dienophiles are discussed. Utilization of 4-acetylfuro[3,2-b]pyrroles for preparation of 4-substituted derivatives of furo[3,2-b]pyrrole and the synthesis of ethyl 4-(2- and 4-nitrobenzyl)furo[3,2-b]pyrrole-5-carboxylates for fusing to a 1,4-diazepine system is presented.

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19

Juneja, T. R., Anju Bala, Punit Kumar, and R. L. Gupta. "Mutagenicity of nitrobenzyl derivatives: potential bioreductive anticancer agents." Mutation Research Letters 348, no. 3 (1995): 137–45. http://dx.doi.org/10.1016/0165-7992(95)00058-5.

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20

Zhou, Ying, Kondapa Naidu Bobba, Xue Wei Lv, et al. "A biotinylated piperazine-rhodol derivative: a ‘turn-on’ probe for nitroreductase triggered hypoxia imaging." Analyst 142, no. 2 (2017): 345–50. http://dx.doi.org/10.1039/c6an02107g.

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21

Wan, Peter, and Keith Yates. "Photoredox chemistry of nitrobenzyl alcohols in aqueous solution. Acid and base catalysis of reaction." Canadian Journal of Chemistry 64, no. 10 (1986): 2076–86. http://dx.doi.org/10.1139/v86-343.

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The photochemistry of several m- and p-nitrobenzyl alcohols (1–5) has been studied in aqueous solution. These compounds react via an intramolecular photoredox pathway to give reduced and oxidized moieties of the substituent groups. The reaction is an example of a new type of photoreaction of nitro-substituted aromatic derivatives that is not observed in organic solvents, the presence of water being essential. This effect is exemplified by measuring the quantum efficiency as a function of mol% water in aqueous acetonitrile, methanol, and formamide: the reaction efficiency decreases rapidly as w

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22

Oluwafemi, Kola A. "Synthesis of n-alkylated azabenzimidazoles, the base catalyzed isomerization of n-propagyl-allenyl azabenzimidazole and 1 their characterization." Ife Journal of Science 22, no. 3 (2021): 175–81. http://dx.doi.org/10.4314/ijs.v22i3.15.

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N-Allyl, N-pentyl, N-propiophenone, N-benzyl, N-p-nitrobenzyl, N-3,4-dichlorobenzyl and N-propargylsubstituted 7-azabenzimidazoles were prepared through a convenient method. Under basic condition, the Npropargyl substituted azabenzimidazole isomerized to its N-allenyl substituted isomer. It is believed that the Nallenyl isolated can serve as a vital precursor for the future preparation of medicinally bioactive cycloaddition derivatives of azabenzimidazole. Key words: Azabenzimidazoles, N-Alkylation, Propargyl, Allene, Isomerization.

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23

Mohamed, Malik Suliman, Toshihide Maki, Mohammad Monir Shah, and Yoshio Ichinose. "Synthesis and Antimicrobial Activity of Nitrobenzyl-oxy-phenol Derivatives." Biological & Pharmaceutical Bulletin 39, no. 11 (2016): 1888–92. http://dx.doi.org/10.1248/bpb.b16-00608.

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24

Blanc, Aurélien, and Christian G. Bochet. "Isotope Effects in Photochemistry. 1.o-Nitrobenzyl Alcohol Derivatives." Journal of the American Chemical Society 126, no. 23 (2004): 7174–75. http://dx.doi.org/10.1021/ja049686b.

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25

Wieboldt, Raymond, Doraiswamy Ramesh, Evelyn Jabri, P. Andrew Karplus, Barry K. Carpenter, and George P. Hess. "Synthesis and Characterization of Photolabileo-Nitrobenzyl Derivatives of Urea." Journal of Organic Chemistry 67, no. 25 (2002): 8827–31. http://dx.doi.org/10.1021/jo0201373.

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26

Myatt, Elizabeth A., and Ioannis Scarpa. "Effects of Polyethyleneimine Derivatives on 2-Hydroxy-5-Nitrobenzyl Ionization." Journal of Macromolecular Science, Part A 29, no. 2 (1992): 153–60. http://dx.doi.org/10.1080/10101329208052158.

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27

Tyrała, Andrzej, and Mieczysław Makosza. "Simple Synthesis of 2-Nitronaphthalene Derivatives from Substitutedp-Nitrobenzyl Sulfones." Synthesis 1994, no. 03 (1994): 264–66. http://dx.doi.org/10.1055/s-1994-35866.

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28

Houlihan, F. M. "Characterization of novel sulfonic acid photogenerating 2-nitrobenzyl ester derivatives." Journal of Vacuum Science & Technology B: Microelectronics and Nanometer Structures 8, no. 6 (1990): 1461. http://dx.doi.org/10.1116/1.585097.

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29

Rafizadeh, Karim, and Keith Yates. "Acid-catalyzed photooxidation of m-nitrobenzyl derivatives in aqueous solution." Journal of Organic Chemistry 51, no. 14 (1986): 2777–81. http://dx.doi.org/10.1021/jo00364a029.

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30

Zhao, Hui, Elizabeth S. Sterner, E. Bryan Coughlin, and Patrick Theato. "o-Nitrobenzyl Alcohol Derivatives: Opportunities in Polymer and Materials Science." Macromolecules 45, no. 4 (2012): 1723–36. http://dx.doi.org/10.1021/ma201924h.

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31

Li, Huiying, Weijun Tong, and Changyou Gao. "Photo-responsive polyethyleneimine microcapsules cross-linked by ortho -nitrobenzyl derivatives." Journal of Colloid and Interface Science 463 (February 2016): 22–28. http://dx.doi.org/10.1016/j.jcis.2015.10.041.

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32

Halgren, Robert G., Ann E. Traynor, Shafali Pillay, et al. "8Cl-cAMP Cytotoxicity in Both Steroid Sensitive and Insensitive Multiple Myeloma Cell Lines Is Mediated by 8Cl-Adenosine." Blood 92, no. 8 (1998): 2893–98. http://dx.doi.org/10.1182/blood.v92.8.2893.

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Abstract We have examined the cytotoxic effects of cyclic adenosine-3′,5′-monophosphate (cAMP) derivatives on multiple myeloma cells lines and determined that the 8-Chloro substituted derivative (8Cl-cAMP) is one of the most potent. We report here that 8Cl-cAMP is cytotoxic to both steroid sensitive and insensitive myeloma cells with a half maximal concentration of approximately 3 μmol/L. 8Cl-cAMP toxicity in myeloma cells is dependent on phosphodiesterase activity in the serum of cell culture medium. A metabolite of 8Cl-cAMP, 8-Chloro-adenosine (8Cl-AD), kills myeloma cells as effectively as

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33

Halgren, Robert G., Ann E. Traynor, Shafali Pillay, et al. "8Cl-cAMP Cytotoxicity in Both Steroid Sensitive and Insensitive Multiple Myeloma Cell Lines Is Mediated by 8Cl-Adenosine." Blood 92, no. 8 (1998): 2893–98. http://dx.doi.org/10.1182/blood.v92.8.2893.420k01_2893_2898.

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We have examined the cytotoxic effects of cyclic adenosine-3′,5′-monophosphate (cAMP) derivatives on multiple myeloma cells lines and determined that the 8-Chloro substituted derivative (8Cl-cAMP) is one of the most potent. We report here that 8Cl-cAMP is cytotoxic to both steroid sensitive and insensitive myeloma cells with a half maximal concentration of approximately 3 μmol/L. 8Cl-cAMP toxicity in myeloma cells is dependent on phosphodiesterase activity in the serum of cell culture medium. A metabolite of 8Cl-cAMP, 8-Chloro-adenosine (8Cl-AD), kills myeloma cells as effectively as 8Cl-cAMP.

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34

Burka, John F. "Studies on a modulatory role for adenosine in antigen and arachidonic acid induced contractions of guinea pig airways." Canadian Journal of Physiology and Pharmacology 64, no. 3 (1986): 225–30. http://dx.doi.org/10.1139/y86-035.

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The modulatory effects of adenosine and selected derivatives were examined on antigen and arachidonic acid (AA) induced contractions of indomethacin-treated tracheal spirals and lung parenchymal strips from actively sensitized guinea pigs. Adenosine (up to 2 × 10−4 M) had no effect on antigen-induced contractions, but inhibited AA-induced contractions by 30–40% if added 30 min prior to challenge. The weak effect of adenosine suggests that endogenous adenosine may only have a limited modulatory role in allergic bronchospasm. 2-Chloroadenosine (10−6–10−4 M) dose-dependently inhibited antigen- an

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35

Meyer, Daniel, Bernard Witholt, and Andreas Schmid. "Suitability of Recombinant Escherichia coli and Pseudomonas putida Strains for Selective Biotransformation of m-Nitrotoluene by Xylene Monooxygenase." Applied and Environmental Microbiology 71, no. 11 (2005): 6624–32. http://dx.doi.org/10.1128/aem.71.11.6624-6632.2005.

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ABSTRACT Escherichia coli JM101(pSPZ3), containing xylene monooxygenase (XMO) from Pseudomonas putida mt-2, catalyzes specific oxidations and reductions of m-nitrotoluene and derivatives thereof. In addition to reactions catalyzed by XMO, we focused on biotransformations by native enzymes of the E. coli host and their effect on overall biocatalyst performance. While m-nitrotoluene was consecutively oxygenated to m-nitrobenzyl alcohol, m-nitrobenzaldehyde, and m-nitrobenzoic acid by XMO, the oxidation was counteracted by an alcohol dehydrogenase(s) from the E. coli host, which reduced m-nitrobe

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36

Gendvilienė, Vida, Danguolė Zablockaitė, Irma Martišienė, Herta Gurskaitė, and Antanas Stankevičius. "Anticholinergic effect of 2-aminopyridine and its sulfonylcarbamide derivatives on electromechanical activity in guinea pig atrium." Medicina 43, no. 10 (2007): 808. http://dx.doi.org/10.3390/medicina43100104.

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The aim of the study was to investigate an action of 2-aminopyridine and its new sulfonylcarbamide derivatives 2-AP21, 2-AP22, 2-AP26, and 2-AP27 (10–5–10–3 M) on carbachol-induced shortening of action potential duration and reduction of contraction force in guinea pig atrial muscles. Experiments were carried out using a standard method of myocardium electromechanical activity registration. Under control conditions (perfusion of atrial strips with Tyrode solution), an average of action potential duration, measured at 90% (AP90) and 50% (AP50) of repolarization, were 112.32±6.07 ms and 50.21±3.

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37

Jan, Thierry, Béatrice Dupas, Didier Floner, and Claude Moinet. "Electrosynthesis of dibenzonaphthyridine derivatives from 2,2-(2-nitrobenzyl)-2-substituted-acetonitriles." Tetrahedron Letters 43, no. 34 (2002): 5949–52. http://dx.doi.org/10.1016/s0040-4039(02)01248-0.

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38

Nakayama, Koji, Inge Heise, Helmut Görner, and Wolfgang Gärtner. "Peptide Release upon Photoconversion of 2-Nitrobenzyl Compounds into Nitroso Derivatives." Photochemistry and Photobiology 87, no. 5 (2011): 1031–35. http://dx.doi.org/10.1111/j.1751-1097.2011.00957.x.

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39

Gazzaeva, R. A., A. N. Fedotov, E. V. Trofimova, O. A. Popova, S. S. Mochalov, and N. S. Zefirov. "Synthesis of o-nitrosoacylbenzenes from o-nitrobenzyl alcohols and their derivatives." Russian Journal of Organic Chemistry 42, no. 1 (2006): 87–99. http://dx.doi.org/10.1134/s1070428006010143.

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40

Harutyunyan, A. A. "N-(4-methoxy-3-nitrobenzyl) derivatives of some nitrogen-containing heterocycles." Russian Journal of Organic Chemistry 52, no. 1 (2016): 76–79. http://dx.doi.org/10.1134/s1070428016010140.

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41

Kim, Moon Suk, and Scott L. Diamond. "Photocleavage of o-nitrobenzyl ether derivatives for rapid biomedical release applications." Bioorganic & Medicinal Chemistry Letters 16, no. 15 (2006): 4007–10. http://dx.doi.org/10.1016/j.bmcl.2006.05.013.

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42

Houlihan, F. M., T. X. Neenan, E. Reichmanis, et al. "Chemically amplified resists: The chemistry and lithographic characteristics of nitrobenzyl benzenesulfonate derivatives." Journal of Photopolymer Science and Technology 3, no. 3 (1990): 259–73. http://dx.doi.org/10.2494/photopolymer.3.259.

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43

Li, Huiying, Yu Xiong, Yixian Zhang, et al. "Photo-Decomposable Sub-Micrometer Albumin Particles Cross-Linked by ortho -Nitrobenzyl Derivatives." Macromolecular Chemistry and Physics 218, no. 24 (2017): 1700413. http://dx.doi.org/10.1002/macp.201700413.

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44

Ram, Siya. "SYNTHESIS OF 4-(NITROBENZYL- AND BENZOYL)PIPERIDINE DERIVATIVES BY NITRATION OF ARYLALKYLPIPERIDINES." Organic Preparations and Procedures International 26, no. 4 (1994): 421–28. http://dx.doi.org/10.1080/00304949409458032.

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45

Smrečki, Neven, Igor Rončević, and Zora Popović. "Vibrational Spectroscopic Characterization and DFT Study of Palladium(II) Complexes with N-Benzyliminodiacetic Acid Derivatives." Australian Journal of Chemistry 69, no. 11 (2016): 1285. http://dx.doi.org/10.1071/ch16150.

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The reactions of N-benzyliminodiacetic acid (BnidaH2) and its para-substituted derivatives, namely N-(p-chlorobenzyl)iminodiacetic acid (p-ClBnidaH2), N-(p-nitrobenzyl)iminodiacetic acid (p-NO2BnidaH2), and N-(p-methoxybenzyl)iminodiacetic acid (p-MeOBnidaH2) with sodium tetrachloropalladate(II) were performed in aqueous solutions. Three new complexes [Pd(p-ClBnidaH)2]·2H2O (2), [Pd(p-NO2BnidaH)2]·2H2O (3), and [Pd(p-MeOBnidaH)2] (4) were prepared and characterized by infrared spectroscopy and thermogravimetric and differential thermal analyses. The molecular geometry and infrared spectra of t

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Peng, Ling, Jakob Wirz, and Maurice Goeldner. "2-Nitrobenzyl Quaternary Ammonium Derivatives Photoreleasing Nor-butyrylcholine in the Microsecond Time Range." Tetrahedron Letters 38, no. 17 (1997): 2961–64. http://dx.doi.org/10.1016/s0040-4039(97)00533-9.

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Šolomek, Tomáš, Christian G. Bochet, and Thomas Bally. "The Primary Steps in Excited-State Hydrogen Transfer: The Phototautomerization ofo-Nitrobenzyl Derivatives." Chemistry - A European Journal 20, no. 26 (2014): 8062–67. http://dx.doi.org/10.1002/chem.201303338.

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TYRALA, A., and M. MAKOSZA. "ChemInform Abstract: Simple Synthesis of 2-Nitronaphthalene Derivatives from Substituted p- Nitrobenzyl Sulfones." ChemInform 25, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.199436129.

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Jan, Thierry, Beatrice Dupas, Didier Floner, and Claude Moinet. "ChemInform Abstract: Electrosynthesis of Dibenzonaphthyridine Derivatives from 2,2-(2-Nitrobenzyl)-2-substituted-acetonitriles." ChemInform 33, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.200245128.

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Hirota, S., T. Okuno, and O. Yamauchi. "Studies on the protein structure of cytochrome c by introducing photo-cleavable o-nitrobenzyl derivatives." Seibutsu Butsuri 39, supplement (1999): S160. http://dx.doi.org/10.2142/biophys.39.s160_1.

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