Log in

Relevant bibliographies by topics / Bromomethyl / Journal articles

To see the other types of publications on this topic, follow the link: Bromomethyl.

Journal articles on the topic 'Bromomethyl'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Bromomethyl.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Jones, Peter G., Piotr Kuś та Ina Dix. "X-Ray Structure Determinations of Bromo- and/or Bromomethylsubstituted Benzenes: C–H···Br, C–Br···Br, and C–Br···π Interactions". Zeitschrift für Naturforschung B 67, № 12 (2012): 1273–81. http://dx.doi.org/10.5560/znb.2012-0249.

Full text

Abstract:

The structures of seven benzene derivatives [1,2,3-tri(bromomethyl)benzene, (1); 3,5- di(bromomethyl)bromobenzene, (2); 2,5-di(bromomethyl)bromobenzene, (3); 4-(bromomethyl)-2,5- dibromotoluene, (4); 4-(bromomethyl)bromobenzene, (5); 2,3-di(bromomethyl)bromobenzene, (6) and (bromomethyl)-p-dibromobenzene, (7)] with bromo and bromomethyl (and in one case methyl) substituents are presented and analysed in terms of Br···Br interactions up to 4.0 A° , supported by hydrogen bonds H···Br. Some interactions of the type Br···π and π···π are encountered and play a subordinate role in the packing. Despi

APA, Harvard, Vancouver, ISO, and other styles

2

Jones, Peter G., та Piotr Kuś. "Secondary Interactions in Bromomethyl-substituted Benzenes: Crystal Structures of Three α,α′-Bis-bromoxylenes, 1,2,3,5-Tetrakis(bromomethyl)benzene, and 1,2,4,5-Tetrakis(bromomethyl)benzene". Zeitschrift für Naturforschung B 62, № 5 (2007): 725–31. http://dx.doi.org/10.1515/znb-2007-0517.

Full text

Abstract:

Abstract X-Ray structure determinations of all three isomers of bis(bromomethyl)benzene and of two isomeric tetrakis(bromomethyl)benzenes show that the packing of the molecules is determined principally by interactions of the bromomethyl groups (C-H· · ·Br and Br· · ·Br), except for ortho-bis (bromomethyl)benzene, in which C-H· · ·π interactions play a major role.

APA, Harvard, Vancouver, ISO, and other styles

3

Brecknell, Douglas J., Raymond M. Carman, Ross A. Edwards, Karl A. Hansford, Tomislav Karoli, and Ward T. Robinson. "Halogenated Terpenoids. XXIX The 1-Bromo 1-Bromomethyl Cyclohexyl System." Australian Journal of Chemistry 50, no. 7 (1997): 689. http://dx.doi.org/10.1071/c96188.

Full text

Abstract:

Bromination of methylene groups exocyclic to cyclohexyl systems normally affords two isomeric products; the axial 1-bromo equatorial 1-bromomethyl compound and the axial 1-bromomethyl equatorial 1-bromo derivative. Free energy differences between these two isomers, and the conformations adopted by the axial 1-bromomethyl group, have been explored by n.m.r. spectroscopy, by X-ray crystallography and by MM3 calculations. Evidence is presented to show that the ax-bromomethyl group exists primarily as those rotamers which site the bromine atom synclinal to the vicinal bromine. The A value for a br

APA, Harvard, Vancouver, ISO, and other styles

4

Papavassiliou, G. C., G. A. Mousdis, and I. B. Koutselas. "Some Organic-Inorganic Hybrid Compounds Based on iso– Thiuronium Cations and Lead Halide Anions." Zeitschrift für Naturforschung B 56, no. 1 (2001): 57–61. http://dx.doi.org/10.1515/znb-2001-0109.

Full text

Abstract:

Abstract Using 1-chlorodecane (C10H21CI), benzyl chloride (C6H5CH2CI), a,a'-dichloro-p-xylene (CICH2C6H4CH2CI), 4-phenylbenzyl chloride (C6H5C6H4CH2CI), 2-bromomethyl-naphthal-ene (C10H7CH2Br), 4-bromomethyl-7-methoxycoumarin (C10H7O3CH2Br), 2-bromomethyl-anthraquinone (C14H7CH2Br), 9-chloromethyl-anthracene (C14H9CH2CI), thiourea and halides as starting materials, the organic-inorganic hybrid compounds [C10H21SC(NH2)2]2Pbl4, [C6H5CH2SC(NH2)2]4Pb3l10 [(H2N2)CSCH2C6H4CH2SC(NH2)2]0.5PbI3, [C6H5C6H4CH2S-C(NH2)2]PbI3, [C10H7CH2SC(NH2)2]Pbl3, [C14H7 O2CH2SC(NH2)2]Pbl3, [C14H9CH2SC(NH2)2]PbI3, and [

APA, Harvard, Vancouver, ISO, and other styles

5

Nestler, Robert, Anke Schwarzer, and Tobias Gruber. "Different supramolecular interactions mediated by Br atoms in the crystal structures of three anisole derivatives." Acta Crystallographica Section C Structural Chemistry 74, no. 3 (2018): 283–88. http://dx.doi.org/10.1107/s2053229618001997.

Full text

Abstract:

Three anisole building blocks featuring bis(hydroxymethyl) or bis(bromomethyl) pendants have been analyzed with regard to their molecular structures and packing behaviour. The compounds are ethyl 3,5-bis(hydroxymethyl)-4-methoxybenzoate, C12H16O5, (I), [5-bromo-3-(hydroxymethyl)-2-methoxyphenyl]methanol [or 4-bromo-2,6-bis(hydroxymethyl)anisole], C9H11BrO3, (II), and 5-bromo-1,3-bis(bromomethyl)-2-methoxybenzene [or 4-bromo-2,6-bis(bromomethyl)anisole], C9H9Br3O, (III). A typical supramolecular pattern involved C—H...π interactions generating molecular stacks, while π–π interactions were only

APA, Harvard, Vancouver, ISO, and other styles

6

Fletcher Claville, Michelle O., Roosevelt J. Payne, Brandon C. Parker, and Frank R. Fronczek. "(Bromomethyl)trimethylammonium bromide." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (2007): o2601. http://dx.doi.org/10.1107/s1600536807018235.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Fletcher Claville, Michelle O., Roosevelt J. Payne, and Frank R. Fronczek. "(Bromomethyl)trimethylammonium tetrafluoroborate." Acta Crystallographica Section E Structure Reports Online 62, no. 8 (2006): o3452—o3454. http://dx.doi.org/10.1107/s1600536806027188.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Černochová, Jarmila, Andrea Čablová, Michal Rouchal, Marek Nečas, and Robert Vícha. "1-(Bromomethyl)adamantane." Acta Crystallographica Section E Structure Reports Online 67, no. 7 (2011): o1820. http://dx.doi.org/10.1107/s1600536811023695.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Xu, Wei-Jian, Yang-Ling Zang, Guo-Liang Wu, Sheng-Pei Su, and De-Yue Qiu. "4-(Bromomethyl)benzophenone." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (2007): o1188—o1189. http://dx.doi.org/10.1107/s160053680700534x.

Full text

Abstract:

The title compound, C14H11BrO, was synthesized by the reaction of 4-methylbenzophenone and bromine in carbon tetrachloride. X-ray crystal structure analysis reveals that the benzene and phenyl rings form a dihedral angle of 59.53 (6)°, and the crystal packing is stabilized by intermolecular C—H...π interactions.

APA, Harvard, Vancouver, ISO, and other styles

10

Guo, Jianyu, Yan Lu, and Jin Wang. "Efficient synthesis of 3-(bromomethyl)-5-methylpyridine hydrobromide." Heterocyclic Communications 21, no. 4 (2015): 203–5. http://dx.doi.org/10.1515/hc-2015-0107.

Full text

Abstract:

Abstract5-Methyl-3-(bromomethyl)pyridine is the key intermediate in the synthesis of rupatadine. In this article, a new preparation of 5-methyl-3-(bromomethyl)pyridine hydrobromide is reported, which used 5-methylnicotinic acid as the starting material, with a 65.9% overall yield. This method has the merits of being simple, efficient and environmentally friendly.

APA, Harvard, Vancouver, ISO, and other styles

11

Morgans, G. L., W. A. L. van Otterlo, J. P. Michael, and M. A. Fernandes. "1-[3,5-Bis(bromomethyl)-2,4,6-trimethoxybenzyl]-3,5-bis(bromomethyl)-2,4,6-trimethoxybenzene." Acta Crystallographica Section E Structure Reports Online 62, no. 1 (2005): o168—o170. http://dx.doi.org/10.1107/s1600536805040559.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Amosova, Svetlana V., Andrey S. Filippov, Nataliya A. Makhaeva, Alexander I. Albanov, and Vladimir A. Potapov. "Green Organoselenium Chemistry: Selective Syntheses of New 1,4-Thiaselenine Derivatives Based on Reactions of Thiaselenole Reagent with Alcohols and Water." Inorganics 11, no. 7 (2023): 281. http://dx.doi.org/10.3390/inorganics11070281.

Full text

Abstract:

Environmentally friendly synthetic methods were developed for the selective preparation of new 2,3-dihydro-1,4-thiaselenine derivatives in high yields based on the reactions of 2-bromomethyl-1,3-thiaselenole with alcohols and water at room temperature. The reaction of 2-bromomethyl-1,3-thiaselenole with alcohols was accompanied by a rearrangement with ring extension, leading to six-membered heterocyclic compounds, a new family of 2-organyloxy-2,3-dihydro-1,4-thiaselenines, in 80–96% yields. The remarkable cascade reactions of 2-bromomethyl-1,3-thiaselenole with water afforded 2,3-dihydro-1,4-t

APA, Harvard, Vancouver, ISO, and other styles

13

Yathirajan, H. S., S. Bindya, B. K. Sarojini, B. Narayana, and Michael Bolte. "Methyl 4-(bromomethyl)benzoate." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (2007): o1334—o1335. http://dx.doi.org/10.1107/s1600536807007258.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Chinnakali, K., H. K. Fun, I. A. Razak, K. Sriraghavan, and V. T. Ramakrishnan. "4-Bromomethyl-7,8-benzocoumarin." Acta Crystallographica Section C Crystal Structure Communications 53, no. 12 (1997): IUC9700030. http://dx.doi.org/10.1107/s0108270197099265.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Betz, Richard, and Peter Klüfers. "1-Bromomethyl-2-iodobenzene." Acta Crystallographica Section E Structure Reports Online 63, no. 12 (2007): o4753. http://dx.doi.org/10.1107/s1600536807058151.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Gowda, Ramakrishna, K. V. Arjuna Gowda, Mahantesha Basanagouda, and Manohar V. Kulkarni. "4-Bromomethyl-7,8-dimethylcoumarin." Acta Crystallographica Section E Structure Reports Online 66, no. 12 (2010): o3352. http://dx.doi.org/10.1107/s1600536810049135.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Fernandes, José A., Sérgio M. F. Vilela, Paulo J. A. Ribeiro-Claro, and Filipe A. Almeida Paz. "1,3,5-Tris(bromomethyl)benzene." Acta Crystallographica Section C Crystal Structure Communications 67, no. 6 (2011): o198—o200. http://dx.doi.org/10.1107/s0108270111013618.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Kuś, Piotr, and Peter G. Jones. "1,6,7-Tris(bromomethyl)naphthalene." Acta Crystallographica Section E Structure Reports Online 59, no. 6 (2003): o899—o900. http://dx.doi.org/10.1107/s160053680301136x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Cuzan, Olesea, Tatiana Straistari, Constantin Turta, and Marius Réglier. "2,6-Bis(bromomethyl)pyridine." Acta Crystallographica Section E Structure Reports Online 70, no. 1 (2013): o4. http://dx.doi.org/10.1107/s1600536813032364.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Mosher, Michael D., Amber L. Norman, and Khriesto A. Shurrush. "5-Bromomethyl-4,5-dihydroisoxazoles." Tetrahedron Letters 50, no. 40 (2009): 5647–48. http://dx.doi.org/10.1016/j.tetlet.2009.07.106.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Wang, Zhi-Guo, Yu-Zhou Wang, Neng-Fang She, and Meng Gao. "1,2,4,5-Tetrakis(bromomethyl)benzene." Acta Crystallographica Section E Structure Reports Online 62, no. 11 (2006): o5106—o5107. http://dx.doi.org/10.1107/s1600536806042334.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Li, Qing-Xiang, Li Cai, Xiu-Feng Wang, and Yun-Jun Shen. "1,1-Bis(bromomethyl)benzene." Acta Crystallographica Section E Structure Reports Online 62, no. 12 (2006): o5726—o5727. http://dx.doi.org/10.1107/s1600536806048422.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Zhang, Min, Ping Su, Xiang-Gao Meng, and Xing-Man Xu. "1,4-Bis(bromomethyl)benzene." Acta Crystallographica Section E Structure Reports Online 63, no. 2 (2007): o951—o952. http://dx.doi.org/10.1107/s1600536807002954.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Skibiński, Maciej, Vladimir A. Azov, and Peter G. Jones. "2,3,6,7-Tetrakis(bromomethyl)naphthalene." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1846—o1847. http://dx.doi.org/10.1107/s1600536810024311.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Kuś, Piotr, Aleksander Zemanek, and Peter G. Jones. "2,5-Bis(bromomethyl)biphenyl." Acta Crystallographica Section E Structure Reports Online 65, no. 6 (2009): o1327. http://dx.doi.org/10.1107/s1600536809018066.

Full text

Abstract:

In the title compound, C14H12Br2, the Br atoms lie on opposite sides of their ring plane. The biphenyl interplanar angle is 53.52 (8)°. The packing is characterized by several H...Br contacts to each Br atom, but at long distances of 3.07–3.43 Å.

APA, Harvard, Vancouver, ISO, and other styles

26

Sasagawa, Kosuke, Daichi Hijikata, Akiko Okamoto, Hideaki Oike, and Noriyuki Yonezawa. "{8-[4-(Bromomethyl)benzoyl]-2,7-dimethoxynaphthalen-1-yl}[4-(bromomethyl)phenyl]methanone." Acta Crystallographica Section E Structure Reports Online 67, no. 8 (2011): o2119. http://dx.doi.org/10.1107/s1600536811029151.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Huang, Chi Bao, Dao Sheng Yi, and Tang Mao Liu. "The Molecular Structures of Alpha-Brominated 2,5-Dimethyl-Terephthalonitrile Derivatives and the Dependences of Their Yields on the Reaction Time." Advanced Materials Research 476-478 (February 2012): 1178–85. http://dx.doi.org/10.4028/www.scientific.net/amr.476-478.1178.

Full text

Abstract:

The number and molecular structures of the alpha-brominated 2,5-dimethylterephthalonitrile (DMT) derivatives and the dependences of the yields of derivatives on the reaction time were systematicaly investigated by means of NMR spectroscopy, MS and chromatography. The alpha-brominated DMT derivatives were comprised of 2-bromomethyl-5-methylterephthalonitrile (1), 2,5-bis(bromomethyl)terephthalonitrile (2), 2-(1,1-dibromo)methyl-5-methylterephthalonitrile (3) and 2-bromomethyl-5-(1,1-dibromo)methylterephthalonitrile (4). More than 90 % of DMT mainly transformed swiftly into 1 during the first tw

APA, Harvard, Vancouver, ISO, and other styles

28

Bunce, Richard A., and Brian J. Murray. "SYNTHESIS OF (±)-3-BROMOMETHYL-1,5-HEXADIENE AND (±)-3-BROMOMETHYL-3-METHYL-1,5-HEXADIENE." Organic Preparations and Procedures International 28, no. 1 (1996): 111–15. http://dx.doi.org/10.1080/00304949609355914.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Qian, Ting-Ting, Meng-Jie Hu, Zhifeng Xin, Ai-Quan Jia, and Qian-Feng Zhang. "Alkylation of tetrathiotungstate anions: crystal structures of the alkylthiolatotrithiotungstate complexes [PPh4]2[WS3(Sn Pr)][WS3(Sn Bu)]·½C6H6 and [PPh4][WS3(SCH2C6H4CH2Cl-4)]." Zeitschrift für Naturforschung B 72, no. 2 (2017): 101–6. http://dx.doi.org/10.1515/znb-2016-0181.

Full text

Abstract:

AbstractThe reaction of [PPh4]2[WS4] in CH3CN with excess n-propylbromide or n-butylbromide gave alkylthiolatotrithiotungstate complexes, [PPh4][WS3(SR)] (1: R=n-propyl; 2: R=n-butyl). The analogous reaction with 1-bromomethyl-4-chloromethyl-benzene afforded a benzylthiolatotrithiotungstate complex, [PPh4][WS3(SCH2C6 H4CH2Cl-4)] (3), whereas the reaction with 1,4-bis-bromomethyl-benzene led to isolation of a dinuclear complex [PPh4]2[WS3(μ-SCH2C6H4CH2S)WS3] (4). Complexes 1–4 were characterized spectroscopically and the crystal structures of 1/2·½C6H6 and 3 have been determined by X-ray diffra

APA, Harvard, Vancouver, ISO, and other styles

30

Gaddam, Kishore, Shanker Kanne, Trivikram Reddy Gundala, Yogeshwar Reddy Mamilla, and Gangi Reddy Nallagondu Chinna. "Determination of Possible Potential Genotoxic Impurities in Lenalidomide Drug Substance by Simple RP-HPLC Method." Asian Journal of Chemistry 32, no. 12 (2020): 2965–70. http://dx.doi.org/10.14233/ajchem.2020.22856.

Full text

Abstract:

This study is concerned with development and validation of HPLC method for the simultaneous detection and quantification of methyl 2-(chloromethyl)-3-nitrobenzoate (MCN), methyl 2-(bromomethyl)-5-nitrobenzoate (MMM), methyl 2-(bromomethyl)-6-nitrobenzoate (MON), methyl 2-(bromomethyl)-4-nitrobenzoate (MPN) and 2-methyl-3-nitrobenzoic acid methyl ester (MNM), which are the genotoxic impurities of lenalidomide. Chromatographic separation was accomplished using a Waters HPLC system equipped with Ascentis Express F5 (150 × 4.6 mm, 2.7 μm) using mobile phase composed of solvent A (0.1% perchloric a

APA, Harvard, Vancouver, ISO, and other styles

31

Schlinquer, Claire, Wei-Sheng Huang, Ling Chen, et al. "Rhodium catalysed enantioselective synthesis of mono-(halo)-methyl-cyclopropanes." Organic & Biomolecular Chemistry 17, no. 3 (2019): 472–76. http://dx.doi.org/10.1039/c8ob03041c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Shimizu, Tomoe, Kan Tanaka, Arjun Paudel, and Takehiko Yamato. "Medium-sized cyclophanes — Part 85: Benzylation by 8-(bromomethyl)[2.2]metacyclophanes. Through-space electronic interactions of [2.2]metacyclophane benzyl cations." Canadian Journal of Chemistry 88, no. 5 (2010): 458–62. http://dx.doi.org/10.1139/v10-003.

Full text

Abstract:

TiCl4-mediated Friedel–Crafts benzylation of benzene with 8-(bromomethyl)[2.2]metacyclophanes to afford 8-benzyl[2.2]metacyclophanes is described. Substituent effect through space on the rate of the benzylation of benzene with a bromomethyl group attached on the opposite aromatic ring was first found in this investigation. Interestingly, the introduction of the substituents at the internal position 16 tends to promote the present benzylation reaction rate 1.8–3.8 times. It was found that the benzyl cation intermediate was stabilized by the the direct through-space cation–π interaction among th

APA, Harvard, Vancouver, ISO, and other styles

33

Kohsaka, Yasuhiro, Keito Hagiwara та Keiichiro Ito. "Polymerization of α-(halomethyl)acrylates through sequential nucleophilic attack of dithiols using a combination of addition–elimination and click reactions". Polymer Chemistry 8, № 6 (2017): 976–79. http://dx.doi.org/10.1039/c6py02145j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Arshad, Muhammad Nadeem, Katheryne Zumberge Edson, Scott T. Mough, and K. Travis Holman. "1,3-Bis(bromomethyl)-2-nitrobenzene." Acta Crystallographica Section E Structure Reports Online 66, no. 4 (2010): o834. http://dx.doi.org/10.1107/s160053681000718x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Hauptvogel, Ines Maria, Anke Schwarzer, and Edwin Weber. "1-Bromo-2-(bromomethyl)naphthalene." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (2007): o2106—o2107. http://dx.doi.org/10.1107/s1600536807013669.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Zhu, Peihua, Yanfang Zhao, Haiyan Chen, Qingtao Cui, and Qin Wei. "1,3-Dibenzyloxy-5-(bromomethyl)benzene." Acta Crystallographica Section E Structure Reports Online 65, no. 4 (2009): o823. http://dx.doi.org/10.1107/s1600536809009672.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Zhou, Feng-yan. "1,2-Bis(bromomethyl)-4,5-dimethoxybenzene." Acta Crystallographica Section E Structure Reports Online 65, no. 9 (2009): o2064. http://dx.doi.org/10.1107/s1600536809030001.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Hammershøj, Peter, and Jørn B. Christensen. "2,3-Bis(bromomethyl)-1,4-dimethoxybenzene." Acta Crystallographica Section E Structure Reports Online 61, no. 9 (2005): o2839—o2840. http://dx.doi.org/10.1107/s1600536805025079.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Jones, Peter G., and Piotr Kuś. "2,2′′-Bis(bromomethyl)-p-terphenyl." Acta Crystallographica Section E Structure Reports Online 61, no. 9 (2005): o2947—o2948. http://dx.doi.org/10.1107/s1600536805025614.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Briggs, Jonathan B., Mikaël D. Jazdzyk, and Glen P. Miller. "2,3-Bis(bromomethyl)-1,4-diphenylbenzene." Acta Crystallographica Section E Structure Reports Online 66, no. 1 (2009): o12. http://dx.doi.org/10.1107/s1600536809050764.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Koch, Niklas, Wilhelm Seichter, and Monika Mazik. "1,3,5-Tris(bromomethyl)-2,4,6-trimethoxybenzene." Acta Crystallographica Section E Structure Reports Online 69, no. 5 (2013): o679. http://dx.doi.org/10.1107/s1600536813008441.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Murray, Pieter, Charlotte Willans, Martin W. Bredenkamp, and Jan-André Gertenbach. "2,4,6-Tris(bromomethyl)-1,3,5-trimethylbenzene." Acta Crystallographica Section E Structure Reports Online 63, no. 1 (2006): o224—o225. http://dx.doi.org/10.1107/s1600536806052160.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Chinnakali, K., R. Surendran, M. Pushparani, A. K. Mohanakrishnan, and Hoong-Kun Fun. "2,7-Bis(bromomethyl)-9,9′-diethylfluorene." Acta Crystallographica Section E Structure Reports Online 63, no. 9 (2007): o3826. http://dx.doi.org/10.1107/s1600536807040020.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Odinets, I. L., O. I. Artyushin, S. V. Lenevich, et al. "Selective monoalkylation of phosphorus-substituted CH acids with (bromomethyl)- and 1,4-bis(bromomethyl)benzenes." Russian Chemical Bulletin 53, no. 1 (2004): 219–27. http://dx.doi.org/10.1023/b:rucb.0000024852.47670.5d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Matteson, Donald S. "Preparation and Properties of (Hydroxymethyl)boronic Acid and its Pinanediol Ester." Australian Journal of Chemistry 64, no. 11 (2011): 1425. http://dx.doi.org/10.1071/ch11289.

Full text

Abstract:

Hydrolysis of diisopropyl (bromomethyl)boronate followed by reaction with pinanediol provides an efficient route to pinanediol (hydroxymethyl)boronate (12), a useful intermediate for asymmetric synthesis. The stability of (hydroxymethyl)boronic acid (10) and its ester 12 have been examined by NMR spectroscopy. Heating for 1 h in acidic D2O does not degrade 10 and only affects the pinanediol moiety of 12. Base does not degrade 10 or 12 in several days at 20–25°C, but converts either to DCH2OD and CH3OD in a few h at 90–98°C, with a large H/D isotope effect. Pinanediol (bromomethyl)boronate with

APA, Harvard, Vancouver, ISO, and other styles

46

Häfliger, Joel, Keith Livingstone, Constantin G. Daniliuc та Ryan Gilmour. "Difluorination of α-(bromomethyl)styrenes via I(I)/I(III) catalysis: facile access to electrophilic linchpins for drug discovery". Chemical Science 12, № 17 (2021): 6148–52. http://dx.doi.org/10.1039/d1sc01132d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Nanduri, V. V. S. S. R., A. V. S. S. Prasad, and K. R. Reddy. "SENSITIVE LIQUID CHROMATOGRAPHIC METHODS FOR THE DETERMINATION OF GENOTOXIC IMPURITIES IN LETROZOLE." INDIAN DRUGS 52, no. 03 (2015): 24–27. http://dx.doi.org/10.53879/id.52.03.p0024.

Full text

Abstract:

Sensitive liquid chromatographic methods for the determination of two genotoxic impurities, namely hydrazine hydrate and 4-bromomethyl benzonitrile, in letrozole have been presented. Method-A is the pre-column derivative UFLC method for the determination of hydrazine hydrate with 4-methoxy benzaldehyde in letrozole. The chemistry involved in the derivatization is explained with suitable mechanism. Method-B offers the determination of 4-bromomethyl benzonitrile in letrozole. Both the methods were validated as per International Conference on Harmonization guidelines. Correlation coefficient valu

APA, Harvard, Vancouver, ISO, and other styles

48

Hudhomme, P., S. G. Liu, D. Kreher, M. Cariou, and A. Gorgues. "New versatile building blocks in tetrathiafulvalene (TTF) chemistry: 2,3-bis(bromomethyl) and tetrakis(bromomethyl)TTFs." Tetrahedron Letters 40, no. 15 (1999): 2927–30. http://dx.doi.org/10.1016/s0040-4039(99)00325-1.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

BUNCE, R. A., and B. J. MURRAY. "ChemInform Abstract: Synthesis of (.+-.)-3-Bromomethyl-1,5-hexadiene and (.+-.)-3- Bromomethyl-3-methyl-1,5-hexadiene." ChemInform 27, no. 26 (2010): no. http://dx.doi.org/10.1002/chin.199626109.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Chen, Rener, Huayue Wu та Yongmin Zhang. "A Novel Synthesis of 1,3-Diketones by Reaction of an α-Bromoketone with Acyl Chlorides Promoted by Gallium Triiodide". Journal of Chemical Research 23, № 11 (1999): 666–67. http://dx.doi.org/10.1177/174751989902301115.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!