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1

Cui, Ning, Junmin Qian, Jinlei Wang, Chuanlei Ji, Weijun Xu, and Hongjie Wang. "Preparation and characterization of foamy poly(γ-benzyl-l-glutamate-co-l-phenylalanine)/bioglass composite scaffolds for bone tissue engineering." RSC Advances 6, no. 77 (2016): 73699–708. http://dx.doi.org/10.1039/c6ra04356a.

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Novel foamy scaffolds of poly(γ-benzyl-l-glutamate) and poly(γ-benzyl-l-glutamate-co-l-phenylalanine) were fabricated via a combination of a sintered NaCl templating method and ring-opening polymerization of α-amino acid N-carboxyanhydrides.
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2

Wang, Xi Ting, Jing Wang, Hai Long Sun, Xiang Yu Du, and Li Fang Ma. "Preparation and properties of poly(benzyl glutamate)-poloxamer-poly(benzyl glutamate) and poly(glutamic acid)-poloxamer-poly(glutamic acid) triblock polymers." Journal of Applied Polymer Science 129, no. 3 (November 27, 2012): 1187–92. http://dx.doi.org/10.1002/app.38601.

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3

Cho, Chong Su, Takashi Takayama, Megumi Kunou, and Toshihiro Akaike. "Platelet adhesion onto the Langmuir-Blodgett film of poly(?-benzylL-glutamate)-poly(ethylene oxide)-poly(?-benzylL-glutamate) block copolymer." Journal of Biomedical Materials Research 24, no. 10 (October 1990): 1369–75. http://dx.doi.org/10.1002/jbm.820241008.

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4

Pytela, Jindřich, František Rypáček, Marie Metalová, and Jaroslav Drobník. "Synthesis of poly[N5-(2-hydroxyethyl)-L-glutamines] with modified side chain." Collection of Czechoslovak Chemical Communications 54, no. 6 (1989): 1640–47. http://dx.doi.org/10.1135/cccc19891640.

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The procedure for synthesis of water-soluble polymers on the basis of poly[N5-(2-hydroxyethyl)-L-glutamine] was developed. It allows binding of various groups of interest (reactive spacers, biologically active compounds, tracers etc.) to these polymers using side chains modifications. A multi-step procedure involves partial debenzylation of poly(γ-benzyl-L-glutamate), conversion of resulting carboxyl groups to reactive succinimido ester groups, which in turn are aminolyzed by the compound of interest. The final step of the synthesis, viz., aminolysis of residual benzyl ester groups with 2-aminoethanol, leads to water-soluble modified poly[N5-(2-hydroxyethyl)-L-glutamines].
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5

Oh, In Joon, Jhin Yee Oh, Chong Su Cho, and Kang Choon Lee. "Biodegradability of poly(γ-benzyl L-glutamate)/poly(ethylene oxide) /poly(γ-benzyl L-glutamate) block copolymer in mice." Archives of Pharmacal Research 18, no. 1 (February 1995): 8–11. http://dx.doi.org/10.1007/bf02976499.

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6

Tang, Dongmei, Jiaping Lin, Shaoliang Lin, Suning Zhang, Tao Chen, and Xiaohui Tian. "Self-Assembly of Poly(γ-benzylL-glutamate)-graft-Poly(ethylene glycol) and Its Mixtures with Poly(γ-benzylL-glutamate) Homopolymer." Macromolecular Rapid Communications 25, no. 13 (July 2004): 1241–46. http://dx.doi.org/10.1002/marc.200400100.

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7

Zhang, Zhi Ming, Shi Qian Wei, Ting Ting Li, and Li Hua Han. "Synthesis of Poly L-Glutamate Initiated by Triethanolamine." Advanced Materials Research 450-451 (January 2012): 26–29. http://dx.doi.org/10.4028/www.scientific.net/amr.450-451.26.

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With L-glutamic acid as raw materials, N-carboxy-L-glutamic acid-benzyl-anhydride (BLG-NCA) was synthesized by triethanolamine. With triethanolamine as the initiator in the anhydrous dichloromethane, ring-opening polymerization of BLG-NCA was initiated, poly-l-glutamic acid benzyl ester was obtained. The amount of initiators, molar ratio of monomer/initiators, reaction temperature and reaction time to the effect of poly-l-glutamic acid benzyl ester in the ring-opening polymerization of BLG-NCA were studied. At last, poly L-glutamate was got, after the debenzylation in HBr solution. Through infrared spectroscopy, Ubbelohde viscometer, 1H NMR spectra, polymerization product was characterized and analysized. Results showed that in dichloromethane, ring-opening polymerization of BLG-NCA could be initiated by triethanolamine.
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8

Cho, Chong-Su, Akira Kobayashi, Mitsuaki Goto, and Toshihiro Akaike. "Orientation of poly(γ-benzyl l-glutamate)/poly(ethylene oxide)/ poly(γ-benzyl l-glutamate) triblock copolymer Langmuir-Blodgett films." Thin Solid Films 264, no. 1 (August 1995): 82–88. http://dx.doi.org/10.1016/0040-6090(95)06506-7.

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9

Kojima, Takakazu, Takuzo Kurotu, Taihei Kawaguchi, and Yoshikiyo Urata. "Thermal decomposition of poly(γ-benzyl-L-glutamate) and γ-benzyl-L-glutamate/γ-methyl-L-glutamate copolymers." Journal of Polymer Science Part A: Polymer Chemistry 26, no. 5 (May 1988): 1479–84. http://dx.doi.org/10.1002/pola.1988.080260520.

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10

Gu, Lin, Yuanzhang Jiang, and Jinlian Hu. "Synthesis and Properties of Shape Memory Poly(γ-Benzyl-l-Glutamate)-b-Poly(Propylene Glycol)-b-Poly(γ-Benzyl-l-Glutamate)." Applied Sciences 7, no. 12 (December 4, 2017): 1258. http://dx.doi.org/10.3390/app7121258.

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11

Li, Yuling, Sai Wang, Dandan Zhu, Yuling Shen, Baixiang Du, Xiaojun Liu, and Yuanlin Zheng. "Reversibly cross-linked poly(ethylene glycol)–poly(amino acid)s copolymer micelles: a promising approach to overcome the extracellular stability versus intracellular drug release challenge." RSC Advances 5, no. 26 (2015): 20025–34. http://dx.doi.org/10.1039/c4ra12255k.

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Reversibly shell cross-linked micelles based on a lipoic acid (LA) decorated triblock copolymer poly(ethylene glycol)-b-poly(γ-benzyl-l-glutamate)-b-poly(l-phenylalanine) have been developed for efficient intracellular delivery of DOX.
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12

Floudas, G., P. Papadopoulos, H. A. Klok, G. W. M. Vandermeulen, and J. Rodriguez-Hernandez. "Hierarchical Self-Assembly of Poly(γ-benzyl-l-glutamate)−Poly(ethylene glycol)−Poly(γ-benzyl-l-glutamate) Rod−Coil−Rod Triblock Copolymers." Macromolecules 36, no. 10 (May 2003): 3673–83. http://dx.doi.org/10.1021/ma025918k.

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13

Parras, P., V. Castelletto, I. W. Hamley, and H. A. Klok. "Nanostructure formation in poly(γ-benzyl-l-glutamate)–poly(ethylene glycol)–poly(γ-benzyl-l-glutamate) triblock copolymers in the solid state." Soft Matter 1, no. 4 (2005): 284. http://dx.doi.org/10.1039/b508772b.

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14

Zhu, Guo-Quan, Fa-Gang Wang, Chang-Hong Su, Qiao-Chun Gao, and Yu-Ying Liu. "Aggregates Morphologies of Poly(g-benzyl L-glutamate)-graft-poly(ethylene glycol) and Poly(g-benzyl L-glutamate) Mixtures in Dilute Solution." Asian Journal of Chemistry 25, no. 6 (2013): 3501–2. http://dx.doi.org/10.14233/ajchem.2013.13485.

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15

Martínez-Barbosa, Ma Elisa, Sandrine Cammas-Marion, Laurent Bouteiller, Christine Vauthier, and Gilles Ponchel. "PEGylated Degradable Composite Nanoparticles Based on Mixtures of PEG-b-Poly(γ-benzyll-glutamate) and Poly(γ-benzyll-glutamate)." Bioconjugate Chemistry 20, no. 8 (August 19, 2009): 1490–96. http://dx.doi.org/10.1021/bc900017c.

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16

Zhu, Guo-Quan, Fa-Gang Wang, Guo-Chang Li, Qiao-Chun Gao, and Yu-Ying Liu. "Self-Assembly of Poly(g-benzyl L-glutamate)-block-poly(ethylene glycol) and Poly(g-benzyl L-glutamate)-graft-poly(ethylene glycol) Blend in Ethanol." Asian Journal of Chemistry 25, no. 6 (2013): 3060–62. http://dx.doi.org/10.14233/ajchem.2013.13517.

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17

Guo-Wang, Pei-Yao, Jian-Xun Ding, Wei Guo, Hui-Yong Wu, Jun-Chao Wei, Yan-Feng Dai, and Feng-Jie Deng. "Silicon dioxide@graphene oxide-graft-poly(γ-benzyl-l-glutamate) as an advanced hybrid nanofiller reinforces poly(l-lactide)." RSC Advances 6, no. 7 (2016): 5688–94. http://dx.doi.org/10.1039/c5ra27104e.

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A novel poly(γ-benzyl-l-glutamate) (PBLG)-modified SiO2@graphene oxide nanofiller (SiO2@GO-g-PBLG) was prepared. The hybrid nanofiller can maintain stable in organic phase, and greatly enhance the mechanical properties of poly(l-lactide).
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18

Colomer, F. Romero, and J. L. Gómez Ribelles. "Structural relaxation of poly(γ-benzyl-l-glutamate)." Polymer 30, no. 5 (May 1989): 849–55. http://dx.doi.org/10.1016/0032-3861(89)90181-x.

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19

Wang, Lianyong, Shenguo Wang, and Jian zhong Bei. "Synthesis and characterization of macroinitiator-amino terminated PEG and poly(?-benzyl-L-glutamate)-PEO-poly(?-benzyl-L-glutamate) triblock copolymer." Polymers for Advanced Technologies 15, no. 10 (October 2004): 617–21. http://dx.doi.org/10.1002/pat.510.

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20

Vacogne, Charlotte D., Sarah M. Brosnan, Admir Masic, and Helmut Schlaad. "Fibrillar gels via the self-assembly of poly(l-glutamate)-based statistical copolymers." Polymer Chemistry 6, no. 28 (2015): 5040–52. http://dx.doi.org/10.1039/c5py00491h.

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21

Dadmun, M. D., M. Muthukumar, D. Schwahn, and T. Springer. "Small-Angle Neutron Scattering of Poly(γ-benzyll-glutamate) in Deuterated Benzyl Alcohol." Macromolecules 29, no. 1 (January 1996): 207–11. http://dx.doi.org/10.1021/ma9500345.

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22

Fang, Jianjun, Qi Yong, Kunxi Zhang, Wentao Sun, Shifeng Yan, Lei Cui, and Jingbo Yin. "Novel injectable porous poly(γ-benzyl-l-glutamate) microspheres for cartilage tissue engineering: preparation and evaluation." Journal of Materials Chemistry B 3, no. 6 (2015): 1020–31. http://dx.doi.org/10.1039/c4tb01333f.

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23

Mori, Akihisa, Yoshihiro Ito, Masahiko Sisido, and Yukio Imanishi. "Interaction of polystyrene/ poly(γ-benzyl l-glutamate) and poly(methyl methacrylate)/ poly(γ-benzyl l-glutamate) block copolymers with plasma proteins and platelets." Biomaterials 7, no. 5 (September 1986): 386–92. http://dx.doi.org/10.1016/0142-9612(86)90010-4.

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24

Zhu, Guo-Quan. "Study on Self-assembly of Poly(ethylene glycol)-block-poly(γ-benzylL-glutamate)-graft-poly(ethylene glycol) Copolymer and Poly(γ-benzylL-glutamate)-block-poly(ethylene glycol) Copolymer in Ethanol." Journal of Macromolecular Science, Part A 46, no. 9 (July 31, 2009): 892–98. http://dx.doi.org/10.1080/10601320903078313.

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25

Zhang, Zhi Ming, Shi Qian Wei, and Li Hua Han. "Study of Synthesis and Properties on Poly L-Glutamate Initiated by Aniline." Advanced Materials Research 284-286 (July 2011): 2110–13. http://dx.doi.org/10.4028/www.scientific.net/amr.284-286.2110.

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With L-glutamic acid as raw materials, N-carboxy-L-glutamic acid-benzyl-anhydride (BLG-NCA) was synthesized by triphosgene. With aniline as the initiator in the anhydrous dichloromethane, ring-opening polymerization of BLG-NCA was initiated, poly-l-glutamic acid benzyl ester was obtained. The amount of initiators, Molar ratio of monomer/initiators, reaction temperature and reaction time to the effect of poly-l-glutamic acid benzyl ester in the ring-opening polymerization of BLG-NCA were studied. Through infrared spectroscopy, gel permeation chromatography (GPC) analysis and characteristic viscosity method, polymerization product was characterized and analysized. Results showed that in dichloromethane, ring-opening polymerization of BLG-NCA could be initiated by aniline, which expands greater scope of the initiators of poly-l-glutamate to aromatic compounds, and the introduction of the active group provided by aromatic compounds make it possible for the advanced development of block copolymer with poly-l-glutamic acid as a basic unit.
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26

Zhu, Guoquan, Fagang Wang, Zhen Ding, Yuying Liu, and Qiaochun Gao. "Aggregation Behavior of Poly(ethylene glycol)-block-poly (γ-benzylL-glutamate)-graft-poly(ethylene glycol) Copolymer and its Blends with Poly(γ-benzylL-glutamate) Homopolymer in Mixed Solvents." Journal of Macromolecular Science, Part A 47, no. 10 (August 31, 2010): 1006–11. http://dx.doi.org/10.1080/10601325.2010.507991.

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27

Kamei, Yasutaka, Atsushi Nagai, Atsushi Sudo, Haruo Nishida, Kiyoshi Kikukawa, and Takeshi Endo. "Convenient synthesis of poly(γ-benzyl-L-glutamate) from activated urethane derivatives of γ-benzyl-L-glutamate." Journal of Polymer Science Part A: Polymer Chemistry 46, no. 8 (2008): 2649–57. http://dx.doi.org/10.1002/pola.22595.

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28

DuPre, Donald B., and Honghui Wang. "Chain dynamics of extended polymers: poly(hexyl isocyanate) and poly(benzyl glutamate)." Macromolecules 25, no. 26 (December 1992): 7155–59. http://dx.doi.org/10.1021/ma00052a013.

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29

Ibarboure, Emmanuel, and Juan Rodríguez-Hernández. "Supramolecular structures from self-assembled poly(γ-benzyl-l-glutamate)–polydimethylsiloxane–poly(γ-benzyl-l-glutamate) triblock copolypeptides in thin films." European Polymer Journal 46, no. 5 (May 2010): 891–99. http://dx.doi.org/10.1016/j.eurpolymj.2010.02.006.

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30

Papadopoulos, P., G. Floudas, I. Schnell, I. Lieberwirth, T. Q. Nguyen, and H. A. Klok. "Thermodynamic Confinement and α-Helix Persistence Length in Poly(γ-benzyl-l-glutamate)-b-poly(dimethyl siloxane)-b-poly(γ-benzyl-l-glutamate) Triblock Copolymers." Biomacromolecules 7, no. 2 (February 2006): 618–26. http://dx.doi.org/10.1021/bm050772t.

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31

LI, Haibin, Zhen TIAN, Meng WANG, Aiying ZHANG, and Zengguo FENG. "SYNTHESIS AND CHARACTERIZATION OF TRIBLOCK COPOLYMERS OF POLY(γ-BENZYL L-GLUTAMATE)-b-POLY(TETRAHYDROFURAN)-b-POLY(γ-BENZYL L-GLUTAMATE)." Acta Polymerica Sinica 006, no. 9 (March 12, 2010): 1117–20. http://dx.doi.org/10.3724/sp.j.1105.2006.01117.

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32

Geng, Dian Guang, Yong Ming Chuan, Li Li Li, and Ming Long Yuan. "The Preparation and Characterization of ABC-Shaped Star Copolymer of MPEG-PCL-PBLG." Advanced Materials Research 750-752 (August 2013): 1358–62. http://dx.doi.org/10.4028/www.scientific.net/amr.750-752.1358.

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A novel biodegradable ABC-shaped star copolymer, poly (ethylene glycol)(PEG)-b-poly (ε-caprolactone)(PCL)-poly-c-poly (ɤ-benzyl-L-glutamic acid)(PBLG)(MPEG-PCL-PBLG), was synthesized by the graft polymerization of MPEG-NH2with the core of Boc-LYSZ-COOH and the twice ring-opening polymerization (ROP) of ε-caprolactone (CL) and N-carboxyanhydride of ɤ-benzyl-L-glutamate (BLGNCA) with centrally amino-functionalized lysine as a initiator. The ABC-shaped star copolymer and its precursors were characterized by1H NMR, GPC, and DSC-TG measurements.
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33

Zhou, Jinglun, Linlin Li, Weishan Wang, Yang Zhao, and Shengyu Feng. "pH-responsive polymeric vesicles from branched copolymers." RSC Advances 9, no. 70 (2019): 41031–37. http://dx.doi.org/10.1039/c9ra08703f.

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A new type of branched copolymer, poly(l-lactide)2-b-poly(l-glutamic acid), based on polypeptide PLGA is synthesized by the ring-opening polymerization of N-carboxyanhydride of γ-benzyl-l-glutamate with amino-terminated PLLA2–NH2 and subsequent deprotection.
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34

Peyret, Ariane, John F. Trant, Colin V. Bonduelle, Khalid Ferji, Namrata Jain, Sebastien Lecommandoux, and Elizabeth R. Gillies. "Synthetic glycopolypeptides: synthesis and self-assembly of poly(γ-benzyl-l-glutamate)-glycosylated dendron hybrids." Polymer Chemistry 6, no. 45 (2015): 7902–12. http://dx.doi.org/10.1039/c5py01060h.

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Polyester dendrons with peripheral α-galactose moieties were synthesized and coupled to poly(γ-benzyl-l-glutamate) to afford amphiphilic linear-dendron hybrid glycopolypeptides that self-assembled in water.
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35

McMaster, T. J., H. J. Carr, M. J. Miles, P. Cairns, and V. J. Morris. "Scanning tunneling microscopy of poly(γ-benzyl L-glutamate)." Macromolecules 24, no. 6 (November 1991): 1428–30. http://dx.doi.org/10.1021/ma00006a037.

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36

Rath, Sujata. "Structural Investigation of Poly(γ-benzyl-L-glutamate) (DP1100)." Polymer Journal 30, no. 12 (December 1998): 950–55. http://dx.doi.org/10.1295/polymj.30.950.

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37

Kiss, Gabor, and Roger S. Porter. "Rheology of concentrated solutions of poly(γ-benzyl-glutamate)." Journal of Polymer Science Part B: Polymer Physics 34, no. 14 (October 1996): 2271–89. http://dx.doi.org/10.1002/polb.1996.938.

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38

Kiss, Gabor, and Roger S. Porter. "Rheology of concentrated solutions of poly(γ-benzyl-glutamate)." Journal of Polymer Science: Polymer Symposia 65, no. 1 (March 8, 2007): 193–211. http://dx.doi.org/10.1002/polc.5070650117.

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39

Yang, David J., Chun Li, Sarah Nikiforow, Matthew B. Gretzer, Li-Ren Kuang, Mona S. Lopez, Sidney Wallace, and Karen Vargas. "Diagnostic and Therapeutic Potential of Poly(benzyl L-glutamate)." Journal of Pharmaceutical Sciences 83, no. 3 (March 1994): 328–31. http://dx.doi.org/10.1002/jps.2600830312.

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40

Tredgold, R. H., and Z. Ali-Adib. "Magnetic alignment of poly(γ-benzyl L-glutamate) films." Journal of Physics D: Applied Physics 21, no. 9 (September 14, 1988): 1467–68. http://dx.doi.org/10.1088/0022-3727/21/9/025.

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41

Marchal, E., and C. Dufour. "Etude des moments dipolaires et des temps de relaxation du poly-l-glutamate de benzyle et de la poly-dl-phenylalanine en chaine en solution diluee." Journal of Polymer Science Part C: Polymer Symposia 30, no. 1 (March 7, 2007): 77–84. http://dx.doi.org/10.1002/polc.5070300109.

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42

Mazzier, D., M. Favaro, S. Agnoli, S. Silvestrini, G. Granozzi, M. Maggini, and A. Moretto. "Synthesis of luminescent 3D microstructures formed by carbon quantum dots and their self-assembly properties." Chem. Commun. 50, no. 50 (2014): 6592–95. http://dx.doi.org/10.1039/c4cc02496f.

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Novel star shaped carbon quantum dots–(poly-γ-benzyl-l-glutamate) conjugates displayed a self-assembling propensity to generate spherical microstructures that retain the characteristic emission properties of the native dots.
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43

Hill, Alyson, and Athene M. Donald. "Gelation in the Poly (γ-Benzyl-L-Glutamate)-Benzyl Alcohol System." Molecular Crystals and Liquid Crystals Incorporating Nonlinear Optics 153, no. 1 (December 1987): 395–404. http://dx.doi.org/10.1080/00268948708074554.

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44

Hill, Alyson, and Athene M. Donald. "Phase behaviour of poly-(λ-benzyl-L-glutamate) in benzyl alcohol." Liquid Crystals 6, no. 1 (January 1989): 93–110. http://dx.doi.org/10.1080/02678298908027326.

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45

Zhu, Guoquan, Qiaochun Gao, Fagang Wang, and Hua Zhang. "Structure and Performance of Poly(vinyl alcohol)/Poly(γ-benzylL-glutamate) Blend Membranes." International Journal of Polymeric Materials 60, no. 9 (August 2011): 720–28. http://dx.doi.org/10.1080/00914037.2010.551357.

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46

Oh, Injoon, Kayoung Lee, Hye-Young Kwon, Yong-Bok Lee, Sang-Chul Shin, Chong-Su Cho, and Chong-Kook Kim. "Release of adriamycin from poly(γ-benzyl-l-glutamate)/poly(ethylene oxide) nanoparticles." International Journal of Pharmaceutics 181, no. 1 (April 1999): 107–15. http://dx.doi.org/10.1016/s0378-5173(99)00012-5.

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47

Ul'yanova, N. N., I. A. Baranovskaya, S. Ya Lyubina, M. A. Byezrukova, G. D. Rudkovskaya, B. M. Shabsel's, G. P. Vlasov, and V. Ye Eskin. "Synthesis of the triblock copolymers poly-γ-benzyl-l-glutamate-PMMA-poly-γ-benzyl-l-glutamate and study of their conformation in solution." Polymer Science U.S.S.R. 32, no. 1 (January 1990): 48–55. http://dx.doi.org/10.1016/0032-3950(90)90045-8.

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48

Shu, Wenchao, Zhen Liu, Yangchun Xie, Xinjie Shi, Shuo Qi, Min Xu, and Xiaohua He. "Regulating the morphology and size of homopolypeptide self-assemblies via selective solvents." Soft Matter 17, no. 30 (2021): 7118–23. http://dx.doi.org/10.1039/d1sm00679g.

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Rod-like micelles including spindles and cylinders with controlling length can be prepared by a solution self-assembly of poly(γ-benzyl-l-glutamate) homopolypeptides with a terminal pyrene group (Py-PBLG) in the selective cosolvents.
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49

Wei, Zheng, Shuzhe Zhu, and Hanying Zhao. "Brush macromolecules with thermo-sensitive coil backbones and pendant polypeptide side chains: synthesis, self-assembly and functionalization." Polymer Chemistry 6, no. 8 (2015): 1316–24. http://dx.doi.org/10.1039/c4py01268b.

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Macromolecular brushes with thermo-sensitive coil backbones and pendant poly(γ-benzyl-l-glutamate) side chains were synthesized by reversible addition–fragmentation chain transfer and ring-opening polymerization. Functionalization and self-assembly of the macromolecules were investigated.
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50

Raby, Philip, Peter M. Budd, Frank Heatley, and Colin Price. "Nuclear magnetic relaxation of α-13C nuclei of helical poly(γ-hexyl-L-glutamate) and poly(γ-benzyl-L-glutamate)." Journal of Polymer Science Part B: Polymer Physics 29, no. 4 (March 30, 1991): 451–56. http://dx.doi.org/10.1002/polb.1991.090290407.

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