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1

Lemmerer, Andreas. "Cyclopropylammonium 4-iodobenzoate." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (2012): o2096. http://dx.doi.org/10.1107/s160053681202449x.

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2

Zhu, Xin, Ping Lu, and Seik Weng Ng. "2-(Tritylsulfanyl)ethyl 2-iodobenzoate." Acta Crystallographica Section E Structure Reports Online 67, no. 9 (2011): o2475. http://dx.doi.org/10.1107/s1600536811034180.

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3

Zhu, Xin, and Seik Weng Ng. "2-(Tritylsulfanyl)ethyl 3-iodobenzoate." Acta Crystallographica Section E Structure Reports Online 67, no. 10 (2011): o2631. http://dx.doi.org/10.1107/s1600536811036427.

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4

Hu, Qing-Ping, Yan Li, Hong-Yu Zhou, Xiu-Fang Zheng, and Ming-Liang Ma. "5-Formyl-2-methoxyphenyl 2-iodobenzoate." Acta Crystallographica Section E Structure Reports Online 62, no. 1 (2005): o109—o110. http://dx.doi.org/10.1107/s1600536805039978.

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5

Hossain, M. Bilayet, and Dick van Der Helm. "The crystal structure of crassin p-iodobenzoate." Recueil des Travaux Chimiques des Pays-Bas 88, no. 12 (2010): 1413–23. http://dx.doi.org/10.1002/recl.19690881206.

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6

Zhu, Mu-Lan, and Ming-Lin Guo. "4-Methylpiperazin-1-ium 2-amino-5-iodobenzoate." Acta Crystallographica Section E Structure Reports Online 61, no. 10 (2005): o3310—o3311. http://dx.doi.org/10.1107/s1600536805029077.

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7

Brock, C. P. "Intermolecular interactions in the structure of methyl 4-iodobenzoate." Acta Crystallographica Section C Crystal Structure Communications 43, no. 9 (1987): 1784–86. http://dx.doi.org/10.1107/s010827018709019x.

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8

Laxminarayana, E., B. Srinivasa Reddy, and Ch Venkata Ramana Reddy. "Development of Green protocols for the synthesis of 1H‐benzo[d]imidazolo aryl amide derivatives and evaluation of their biological activity." Vietnam Journal of Chemistry 58, no. 6 (2020): 779–84. http://dx.doi.org/10.1002/vjch.202000079.

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AbstractBenzimidazole scaffold containing chemical derivatives show superior biological activity. In view of this, we synthesized a combination of benzimidazole and aryl amides. The target compounds (6a‐j) were synthesized using ethyl 3‐iodobenzoate and benzimidazole as starting materials under microwave conditions. The synthesized compounds were screened against gram (+ve) and gram (‐ve) bacteria as well as for their anti‐oxidant activity. Compound 6a was proved to be most active in inhibiting the DPPH free radical.
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9

Vaidyanathan, Ganesan, Donna J. Affleck, and Michael R. Zalutsky. "Radioiodination of proteins using N-succinimidyl 4-hydroxy-3-iodobenzoate." Bioconjugate Chemistry 4, no. 1 (1993): 78–84. http://dx.doi.org/10.1021/bc00019a011.

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10

Xu, Jin-Sheng, Chun-Hua Zhang, Dai-Zhi Kuang та Yong-Lan Feng. "Crystal structure of bis(2,2'-bipyridine)bis(3-iodobenzoate-O,O')tetrakis(μ- 3-iodobenzoate-O,O')disamarium(III), Sm2(C10H8N2)2(C7H4O2I)6". Zeitschrift für Kristallographie - New Crystal Structures 222, № 4 (2007): 442–44. http://dx.doi.org/10.1524/ncrs.2007.0187.

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11

Archana, Sriramapura D., Haruvegowda Kiran Kumar, Hemmige S. Yathirajan, Sabine Foro, Mohammed S. M. Abdelbaky, and Santiago Garcia-Granda. "Crystal structure studies of 4-ethylpiperazin-1-ium 3,5-dinitrobenzoate, 4-methylpiperazin-1-ium 3,5-dinitrobenzoate and 4-methylpiperazin-1-ium 4-iodobenzoate." Acta Crystallographica Section E Crystallographic Communications 77, no. 11 (2021): 1135–39. http://dx.doi.org/10.1107/s2056989021010689.

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As part of our ongoing investigation on the chemical and biological properties of piperazinium salts, we synthesized three novel compounds: 1-ethylpiperazinium 3,5-dinitrobenzoate (I), 1-methylpiperazinium 3,5-dinitrobenzoate (II) and 1-methylpiperazinium 4-iodobenzoate (III). The crystal structures of these compounds are built up of organic layers formed by the strong connection between the molecules by hydrogen bonds of type N—H...O. These layers are linked through N—H...O hydrogen bonds and C—H...O interactions or C—I...N halogen bonding, leading to the formation of a three-dimensional netw
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12

Vaidyanathan, Ganesan, Donna J. Affleck, and Michael R. Zalutsky. "Method for Radioiodination of Proteins UsingN-Succinimidyl 3-Hydroxy-4-iodobenzoate." Bioconjugate Chemistry 8, no. 5 (1997): 724–29. http://dx.doi.org/10.1021/bc9700502.

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13

Chitneni, Satish K., Eftychia Koumarianou, Ganesan Vaidyanathan, and Michael R. Zalutsky. "Observations on the Effects of Residualization and Dehalogenation on the Utility of N-Succinimidyl Ester Acylation Agents for Radioiodination of the Internalizing Antibody Trastuzumab." Molecules 24, no. 21 (2019): 3907. http://dx.doi.org/10.3390/molecules24213907.

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Trastuzumab is an antibody used for the treatment of human epidermal growth factor receptor 2 (HER2)-overexpressing breast cancers. Since trastuzumab is an internalizing antibody, two factors could play an important role in achieving high uptake and prolonged retention of radioactivity in HER2-positive tumors after radioiodination—residualizing capacity after receptor-mediated internalization and susceptibility to dehalogenation. To evaluate the contribution of these two factors, trastuzumab was radiolabeled using the residualizing reagent N-succinimidyl 4-guanidinomethyl-3-[*I]iodobenzoate ([
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14

Bondarenko, Mikhail A., Marianna I. Rakhmanova, Alexander S. Novikov, Maxim N. Sokolov, and Sergey A. Adonin. "Bi- or trinuclear 2-iodobenzoate complexes of Znii: crystal structures and luminescence." Mendeleev Communications 32, no. 5 (2022): 585–87. http://dx.doi.org/10.1016/j.mencom.2022.09.005.

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15

Garg, Pradeep K., Gerald E. Archer, Darell D. Bigner, and Michael R. Zalutsky. "Synthesis of radioiodinated N-succinimidyl iodobenzoate: Optimization for use in antibody labelling." International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes 40, no. 6 (1989): 485–90. http://dx.doi.org/10.1016/0883-2889(89)90131-7.

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16

Hsu, I.-Nan, and Dick van der Helm. "The crystal and molecular structure of the p-iodobenzoate of 23-demethylgorgosterol." Recueil des Travaux Chimiques des Pays-Bas 92, no. 10 (2010): 1134–42. http://dx.doi.org/10.1002/recl.19730921011.

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17

Aydın, Ömür, Nagihan Çaylak Delibaş, Hacali Necefoğlu та Tuncer Hökelek. "Tetrakis(μ-2-iodobenzoato-κ2O:O′)bis[aquacopper(II)]". Acta Crystallographica Section E Structure Reports Online 68, № 4 (2012): m409—m410. http://dx.doi.org/10.1107/s1600536812010367.

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In the centrosymmetric binuclear title complex, [Cu2(C7H4IO2)4(H2O)2], the two CuIIions [Cu...Cu = 2.6009 (5) Å] are bridged by four 2-iodobenzoate (IB) ligands. The four nearest O atoms around each CuIIion form a distorted square-planar arrangement, the distorted square-pyramidal coordination being completed by the O atom of the water molecule at a distance of 2.1525 (16) Å. The dihedral angle between the benzene ring and the carboxylate group is 25.67 (13)° in one of the independent IB ligands and 6.44 (11)° in the other. The benzene rings of the two independent IB ligands are oriented at a
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18

Khawli, Leslie A., and Amin I. Kassis. "Synthesis of 125I labeled N-succinimidyl p-iodobenzoate for use in radiolabeling antibodies." International Journal of Radiation Applications and Instrumentation. Part B. Nuclear Medicine and Biology 16, no. 7 (1989): 727–33. http://dx.doi.org/10.1016/0883-2897(89)90146-3.

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19

Wang, Tao, Patrick Rabe, Christian A. Citron, and Jeroen S. Dickschat. "Halogenated volatiles from the fungusGeniculosporiumand the actinomyceteStreptomyces chartreusis." Beilstein Journal of Organic Chemistry 9 (December 3, 2013): 2767–77. http://dx.doi.org/10.3762/bjoc.9.311.

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Two unidentified chlorinated volatilesXandYwere detected in headspace extracts of the fungusGeniculosporium. Their mass spectra pointed to the structures of a chlorodimethoxybenzene forXand a dichlorodimethoxybenzene forY. The mass spectra of some constitutional isomers forXandYwere included in our databases and proved to be very similar, thus preventing a full structural assignment. For unambiguous structure elucidation all possible constitutional isomers forXandYwere obtained by synthesis or from commercial suppliers. Comparison of mass spectra and GC retention times rigorously established t
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20

Aydın, Ömür, Nagihan Çaylak Delibaş, Hacali Necefoğlu та Tuncer Hökelek. "Diaquabis(2-iodobenzoato-κO)bis(nicotinamide-κN1)cobalt(II)". Acta Crystallographica Section E Structure Reports Online 68, № 4 (2012): m521—m522. http://dx.doi.org/10.1107/s160053681201330x.

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In the title complex, [Co(C7H4IO2)2(C6H6N2O)2(H2O)2], the CoIIcation is located on an inversion center and is coordinated by two monodentate 2-iodobenzoate (IB) anions, two nicotinamide (NA) ligands and two water molecules. The four O atoms in the equatorial plane around the CoIIcation form a slightly distorted square-planar arrangement, while the slightly distorted octahedral coordination is completed by the two N atoms of the NA ligands in the axial positions. The dihedral angle between the carboxylate group and the adjacent benzene ring is 22.3 (3)°, while the pyridine ring and the benzene
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21

Harish Chinthal, Chayanna, Channappa N. Kavitha, Hemmige S. Yathirajan, Sabine Foro, Ravindranath S. Rathore, and Christopher Glidewell. "Fifteen 4-(2-methoxyphenyl)piperazin-1-ium salts containing organic anions: supramolecular assembly in zero, one, two and three dimensions." Acta Crystallographica Section E Crystallographic Communications 76, no. 11 (2020): 1779–93. http://dx.doi.org/10.1107/s2056989020014097.

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Fifteen 4-(2-methoxyphenyl)piperazin-1-ium salts containing organic anions have been prepared and structurally characterized. In the isostructural 4-chlorobenzoate and 4-bromobenzoate salts, C11H17N2O+·C7H4ClO2 − (I) and C11H17N2O+·C7H4BrO2 − (II), and the 4-iodobenzoate salt C11H17N2O+·C7H4IO2 − (III), the ions are linked by N—H...O hydrogen bonds, forming centrosymmetric R 4 4(12) four-ion aggregates; a similar aggregate is formed in the 2-chlorobenzoate salt (V), isomeric with (I). In the 2-fluorobenzoate salt C11H17N2O+·C7H4FO2 − (IV), and the isomorphous pair of salts, the 2-bromobenzoate
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22

Sperry, Jeffrey B., and Karen Sutherland. "A Safe and Practical Procedure for the Difluoromethylation of Methyl 4-Hydroxy-3-iodobenzoate." Organic Process Research & Development 15, no. 3 (2011): 721–25. http://dx.doi.org/10.1021/op200052z.

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23

Guo, Qingliang, Jianmin Dou, Libin Wu, Dacheng Li, and Daqiwang. "Two iso-closo 11-vertex ruthenaborane clusters with exo-polyhedral cyclization of para-iodobenzoate." Journal of Coordination Chemistry 60, no. 7 (2007): 785–94. http://dx.doi.org/10.1080/00958970600918052.

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24

Pruszynski, M., E. Koumarianou, G. Vaidyanathan, et al. "Improved Tumor Targeting of Anti-HER2 Nanobody Through N-Succinimidyl 4-Guanidinomethyl-3-Iodobenzoate Radiolabeling." Journal of Nuclear Medicine 55, no. 4 (2014): 650–56. http://dx.doi.org/10.2967/jnumed.113.127100.

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25

Garg, Pradeep K., Kevin L. Alston, Philip C. Welsh та Michael R. Zalutsky. "Enhanced Binding and Inertness to Dehalogenation of α-Melanotropic Peptides Labeled UsingN-Succinimidyl 3-Iodobenzoate". Bioconjugate Chemistry 7, № 2 (1996): 233–39. http://dx.doi.org/10.1021/bc960001+.

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26

Vaidyanathan, Ganesan, and Michael R. Zalutsky. "Preparation of N-succinimidyl 3-[*I]iodobenzoate: an agent for the indirect radioiodination of proteins." Nature Protocols 1, no. 2 (2006): 707–13. http://dx.doi.org/10.1038/nprot.2006.99.

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27

Lemmerer, Andreas, Susan A. Bourne, and Manuel A. Fernandes. "Disruption of a robust supramolecular heterosynthon in achiral benzylammonium and (pyridylmethyl)ammonium m-iodobenzoate salts." CrystEngComm 10, no. 12 (2008): 1750. http://dx.doi.org/10.1039/b811789f.

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28

Lee, Bae Hoon, Christine Leon, Ryan McLemore, Jorge Valdez Macias, and Brent L. Vernon. "Synthesis and Characterization of Thermo-Sensitive Radio-Opaque Poly(N-Isopropylacrylamide-co-PEG-2-Iodobenzoate)." Journal of Biomaterials Science, Polymer Edition 22, no. 17 (2011): 2357–67. http://dx.doi.org/10.1163/092050610x539541.

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29

Enwall, E. L., and Dick van der Helm. "The crystal structure and absolute configuration of the 3-p-iodobenzoate-11-acetate of secogorgosterol." Recueil des Travaux Chimiques des Pays-Bas 93, no. 2 (2010): 53–56. http://dx.doi.org/10.1002/recl.19740930209.

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30

Beiki, Davood, Soraya Shahhosseini, Ali Khalaj, and Mohammad Eftekhari. "Increased selectivity in inflammatory site identification via labelling of IgG withN-succinimidyl-4-[125I]iodobenzoate." Journal of Labelled Compounds and Radiopharmaceuticals 45, no. 11 (2002): 927–34. http://dx.doi.org/10.1002/jlcr.608.

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31

Mirocki, Artur, and Artur Sikorski. "Influence of Halogen Substituent on the Self-Assembly and Crystal Packing of Multicomponent Crystals Formed from Ethacridine and Meta-Halobenzoic Acids." Crystals 10, no. 2 (2020): 79. http://dx.doi.org/10.3390/cryst10020079.

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In order to determine the influence of halogen substituent on the self-assembly of the 6,9-diamino-2-ethoxyacridinium cations and 3-halobenzoate anions in the crystals formed from ethacridine and halobenzoic acids, the series of ethacridinium meta-halobenzoates dihydrates: ethacridinium 3-chlorobenzoate dihydrate (1), ethacridinium 3-bromobenzoate dihydrate (2), and ethacridinium 3-iodobenzoate dihydrate (3), were synthesized and structurally characterized. Single-crystal X-ray diffraction measurements showed that the title compounds crystallized in the monoclinic P21/c space group and are iso
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32

Touchet, Sabrina, Callum Yeardley, Charles T. O'Hara, and Philippe C. Gros. "Critical Ligand and Salt Effects in Organomagnesiate‐Promoted 3,3‐Disubstituted Phthalides Synthesis from 2‐Iodobenzoate Derivatives." European Journal of Organic Chemistry 2021, no. 34 (2021): 4835–45. http://dx.doi.org/10.1002/ejoc.202100899.

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33

Hassam, Mohammad, Shivaji V. More, and Wen-Shan Li. "Synthesis of nitrogen-containing benzoannulated eight- and nine-membered heterocycles from methyl 4-amino-3-iodobenzoate." Mendeleev Communications 24, no. 3 (2014): 159–60. http://dx.doi.org/10.1016/j.mencom.2014.04.011.

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34

XU, Lijuan, Yanqiu LI, and Xia LI. "Synthesis, crystal structure and characterization of one-dimension complex constructed by terbium(III) and 2-iodobenzoate." Journal of Rare Earths 27, no. 3 (2009): 372–75. http://dx.doi.org/10.1016/s1002-0721(08)60253-7.

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35

Chen, Jianqing, Mengmeng Wang, Alison Joyce, et al. "Comparison of Succinimidyl [125I]Iodobenzoate with Iodogen Iodination Methods to Study Pharmacokinetics and ADME of Biotherapeutics." Pharmaceutical Research 31, no. 10 (2014): 2810–21. http://dx.doi.org/10.1007/s11095-014-1378-3.

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36

Bondarenko, M. A., and S. A Adonin. "CRYSTAL STRUCTURES OF MIXED-LIGAND BINUCLEAR Zn(II) 2-IODOBENZOATE COMPLEXES WITH 4-ETHYL- AND 3-CHLOROPYRIDINE." Journal of Structural Chemistry 62, no. 8 (2021): 1251–56. http://dx.doi.org/10.1134/s0022476621080114.

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37

Abe, Hitoshi, Yasuo Takeuchi, Kazuhiro Maeda, et al. "Regioselectivity of the Intramolecular Biaryl Coupling Reaction of 3-Substituted Phenyl 2-Iodobenzoate using a Palladium Reagent." HETEROCYCLES 88, no. 1 (2014): 621. http://dx.doi.org/10.3987/com-13-s(s)10.

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38

Choi, Jaeyeon, Ganesan Vaidyanathan, Eftychia Koumarianou, et al. "N-Succinimidyl guanidinomethyl iodobenzoate protein radiohalogenation agents: Influence of isomeric substitution on radiolabeling and target cell residualization." Nuclear Medicine and Biology 41, no. 10 (2014): 802–12. http://dx.doi.org/10.1016/j.nucmedbio.2014.07.005.

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39

Al-Jammaz, I., B. Al-Otaibi, and J. K. Amartey. "A novel route to radioiodinated [123I]-N-succinimidyl-3-iodobenzoate, a reagent for radioiodination of bioactive peptides." Applied Radiation and Isotopes 57, no. 5 (2002): 743–47. http://dx.doi.org/10.1016/s0969-8043(02)00191-4.

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40

Al-Jammaz, A., B. Abu Durah, and J. K. Amartey. "A novel route to radioiodinate [123I]-N-succinimidyl-3-iodobenzoate, a reagent for radioiodination of bioactive peptides." Nuclear Medicine Communications 21, no. 6 (2000): 582–83. http://dx.doi.org/10.1097/00006231-200006000-00084.

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41

Vorobyeva, Schulga, Rinne, et al. "Indirect Radioiodination of DARPin G3 Using N-succinimidyl-Para-Iodobenzoate Improves the Contrast of HER2 Molecular Imaging." International Journal of Molecular Sciences 20, no. 12 (2019): 3047. http://dx.doi.org/10.3390/ijms20123047.

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Radionuclide molecular imaging of human epidermal growth factor receptor 2 (HER2) in breast and gastroesophageal cancer might be used to stratify patients for HER2-targeted therapy as well as monitor treatment response and disease progression. Designed ankyrin repeat proteins (DARPins) are small engineered scaffold proteins with favorable properties for molecular imaging. Herein we compared two methods for labeling the anti-HER2 DARPin (HE)3-G3, direct and indirect radioiodination. We hypothesized that the use of N-succinimidyl-para-iodobenzoate (SPIB) for radioiodination would facilitate the
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42

Wardell, James L., Janet M. S. Skakle, John N. Low, and Christopher Glidewell. "4-Nitrophenyl 2-iodobenzoate: sheets built from C—H...O hydrogen bonds and two-centre iodo–nitro interactions." Acta Crystallographica Section E Structure Reports Online 61, no. 10 (2005): o3334—o3336. http://dx.doi.org/10.1107/s1600536805029272.

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43

Koziorowski, J., C. Henssen, and R. Weinreich. "A new convenient route to radioiodinated N-succinimidyl 3- and 4-iodobenzoate, two reagents for radioiodination of proteins." Applied Radiation and Isotopes 49, no. 8 (1998): 955–59. http://dx.doi.org/10.1016/s0969-8043(97)10112-9.

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44

Hassam, Mohammad, Shivaji V. More, and Wen-Shan Li. "ChemInform Abstract: Synthesis of Nitrogen-Containing Benzoannulated Eight- and Nine-Membered Heterocycles from Methyl 4-Amino-3-iodobenzoate." ChemInform 45, no. 42 (2014): no. http://dx.doi.org/10.1002/chin.201442198.

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45

Khalaj, Ali, Davood Beiki, Hamid Rafiee, and Reza Najafi. "A new and simple synthesis of N-succinimidyl-4-[127/125I]iodobenzoate involving a microwave - accelerated iodination step." Journal of Labelled Compounds and Radiopharmaceuticals 44, no. 3 (2001): 235–40. http://dx.doi.org/10.1002/jlcr.451.

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46

Mahesha, Ninganayaka, Haruvegowda Kiran Kumar, Hemmige S. Yathirajan, Sabine Foro, Mohammed S. M. Abdelbaky, and Santiago Garcia-Granda. "Crystal structures of six 4-(4-nitrophenyl)piperazin-1-ium salts." Acta Crystallographica Section E Crystallographic Communications 78, no. 5 (2022): 510–18. http://dx.doi.org/10.1107/s2056989022004157.

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Six piperazinium salts, namely 4-(4-nitrophenyl)piperazin-1-ium 4-bromobenzoate dihydrate, C10H14N3O2 +·C7H4BrO2 −·2H2O, (I), 4-(4-nitrophenyl)piperazin-1-ium 4-iodobenzoate dihydrate, C10H14N3O2 +·C7H4IO2 −·2H2O, (II), 4-(4-nitrophenyl)piperazin-1-ium 4-hydroxybenzoate monohydrate, C10H14N3O2 +·C7H5O3 −·H2O, (III), 4-(4-nitrophenyl)piperazin-1-ium 4-methylbenzoate monohydrate, C10H14N3O2 +·C8H7O2 −·H2O, (IV), 4-(4-nitrophenyl)piperazin-1-ium 4-methoxybenzoate hemihydrate, 2C10H14N3O2 +·2C8H7O3 −·H2O, (V), and 4-(4-nitrophenyl)piperazin-1-ium 4-ethoxybenzoate, 2C10H14N3O2 +·2C9H9O3 −, (VI), ha
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47

Mahesha, Ninganayaka, Haruvegowda Kiran Kumar, Hemmige S. Yathirajan, Sabine Foro, Mohammed S. M. Abdelbaky, and Santiago Garcia-Granda. "Crystal structures of six 4-(4-nitrophenyl)piperazin-1-ium salts." Acta Crystallographica Section E Crystallographic Communications 78, no. 5 (2022): 510–18. http://dx.doi.org/10.1107/s2056989022004157.

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Six piperazinium salts, namely 4-(4-nitrophenyl)piperazin-1-ium 4-bromobenzoate dihydrate, C10H14N3O2 +·C7H4BrO2 −·2H2O, (I), 4-(4-nitrophenyl)piperazin-1-ium 4-iodobenzoate dihydrate, C10H14N3O2 +·C7H4IO2 −·2H2O, (II), 4-(4-nitrophenyl)piperazin-1-ium 4-hydroxybenzoate monohydrate, C10H14N3O2 +·C7H5O3 −·H2O, (III), 4-(4-nitrophenyl)piperazin-1-ium 4-methylbenzoate monohydrate, C10H14N3O2 +·C8H7O2 −·H2O, (IV), 4-(4-nitrophenyl)piperazin-1-ium 4-methoxybenzoate hemihydrate, 2C10H14N3O2 +·2C8H7O3 −·H2O, (V), and 4-(4-nitrophenyl)piperazin-1-ium 4-ethoxybenzoate, 2C10H14N3O2 +·2C9H9O3 −, (VI), ha
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Garg, Pradeep K., Kevin L. Alston, and Michael R. Zalutsky. "Catabolism of radioiodinated murine monoclonal antibody F(ab')2 fragment labeled using N-succinimidyl 3-iodobenzoate and Iodogen methods." Bioconjugate Chemistry 6, no. 4 (1995): 493–501. http://dx.doi.org/10.1021/bc00034a020.

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Kim, Min Hwan, Sang-Keun Woo, Kyo Chul Lee, et al. "Longitudinal monitoring adipose-derived stem cell survival by PET imaging hexadecyl-4-124I-iodobenzoate in rat myocardial infarction model." Biochemical and Biophysical Research Communications 456, no. 1 (2015): 13–19. http://dx.doi.org/10.1016/j.bbrc.2014.11.019.

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Vaidyanathan, Ganesan, and Michael R. Zalutsky. "Synthesis of N-succinimidyl 4-guanidinomethyl-3-[*I]iodobenzoate: a radio-iodination agent for labeling internalizing proteins and peptides." Nature Protocols 2, no. 2 (2007): 282–86. http://dx.doi.org/10.1038/nprot.2007.20.

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