Synthesis of optically active polymers containing a main-chain hydroxamic acid backbone
                    via
                    asymmetric polymerization

Naoya Kanbayashi; Kiyotaka Onitsuka

doi:10.1039/d6py00186f

journal article Jan 01, 2026

Synthesis of optically active polymers containing a main-chain hydroxamic acid backbone via asymmetric polymerization

Naoya Kanbayashi

Kiyotaka Onitsuka

Polymer Chemistry · Royal Society of Chemistry (RSC)

View at Publisher Save 10.1039/d6py00186f

Abstract

Synthesis of an optically active polymer bearing a hydroxamic acid backbone.

Topics

No keywords indexed for this article. Browse by subject →

References

45

[1]

Winter Chem. Soc. Rev. (2016) 10.1039/c6cs00182c

[2]

Abd-El-Aziz Polymer (2012) 10.1016/j.polymer.2012.08.024

[3]

Chen Responsive Mater. (2023) 10.1002/rpm.20230011

[4]

Akine Coord. Chem. Rev. (2022) 10.1016/j.ccr.2022.214582

[5]

Liu Front. Chem. (2020) 10.3389/fchem.2020.589106

[6]

Marsella J. Am. Chem. Soc. (1993) 10.1021/ja00078a090

[7]

Horeau Angew. Chem., Int. Ed. (2017) 10.1002/anie.201701693

[8]

Codd Coord. Chem. Rev. (2008) 10.1016/j.ccr.2007.08.001

[9]

Kurzak Coord. Chem. Rev. (1992) 10.1016/0010-8545(92)85002-8

[10]

Bauer Angew. Chem., Int. Ed. Engl. (1974) 10.1002/anie.197403761

[11]

Yale Chem. Rev. (1943) 10.1021/cr60106a002

[12]

Brown J. Chem. Soc., Perkin Trans. 2 (1996) 10.1039/p29960002673

[13]

Raymond Acc. Chem. Res. (1979) 10.1021/ar50137a004

[14]

Raymond Acc. Chem. Res. (2015) 10.1021/acs.accounts.5b00301

[15]

Neilands Science (1967) 10.1126/science.156.3781.1443

[16]

Finnin Nature (1999) 10.1038/43710

[17]

Richon Proc. Natl. Acad. Sci. U. S. A. (1998) 10.1073/pnas.95.6.3003

[18]

Marks Nat. Biotechnol. (2007) 10.1038/nbt1272

[19]

Vannini Proc. Natl. Acad. Sci. U. S. A. (2004) 10.1073/pnas.0404603101

[20]

Marmion Eur. J. Inorg. Chem. (2004) 10.1002/ejic.200400221

[21]

Li Acc. Chem. Res. (2013) 10.1021/ar300216r

[22]

Winston J. Polym. Sci., Polym. Chem. Ed. (1975) 10.1002/pol.1975.170130906

[23]

Winston Macromolecules (1978) 10.1021/ma60063a033

[24]

Sockwell Chem. – Eur. J. (2019) 10.1002/chem.201803176

[25]

Keth Biomacromolecules (2020) 10.1021/acs.biomac.0c00449

[26]

Johann Macromol. Rapid Commun. (2020) 10.1002/marc.201900282

[27]

Lee Polym. Bull. (1994) 10.1007/bf00308537

[28]

Sarkar J. Catal. (2017) 10.1016/j.jcat.2017.03.023

[29]

Rossi Biomaterials (2009) 10.1016/j.biomaterials.2008.09.057

[30]

Wang Chem. Soc. Rev. (2019) 10.1039/c7cs00656j

[31]

Kanbayashi Angew. Chem., Int. Ed. (2013) 10.1002/anie.201300485

[32]

Kanbayashi Macromolecules (2014) 10.1021/ma5008623

[33]

Kanbayashi Macromolecules (2015) 10.1021/acs.macromol.5b02067

[34]

Kanbayashi Polym. Chem. (2016) 10.1039/c6py00484a

[35]

Kanbayashi Kobunshi Ronbunshu (2017) 10.1295/koron.2017-0027

[36]

Kanbayashi Polym. Chem. (2017) 10.1039/c6py01946c

[37]

Ishido Macromolecules (2017) 10.1021/acs.macromol.7b01426

[38]

Ishido ACS Macro Lett. (2019) 10.1021/acsmacrolett.9b00249

[39]

Ishido Chem. Commun. (2020) 10.1039/c9cc10030j

[40]

Ishido Macromol. Rapid Commun. (2021) 10.1002/marc.202100250

[41]

Yoshino Chem. Pharm. Bull. (1987) 10.1248/cpb.35.3438

[42]

Katahara J. Am. Chem. Soc. (2016) 10.1021/jacs.6b02324

[43]

Lipczynska-Kochany J. Org. Chem. (1982) 10.1021/jo00148a010

[44]

Brown Magn. Reson. Chem. (1988) 10.1002/mrc.1260261107

[45]

García Inorg. Chem. (2003) 10.1021/ic034161q

Metrics

0

Citations

45

References

Details

Published: Jan 01, 2026
License: View

Authors

N

Naoya Kanbayashi

Faculty of Materials Science and Engineering, Kyoto Institute of Technology, Sakyo-ku, Kyoto 606-8585, Japan

K

Kiyotaka Onitsuka

Department of Macromolecular Science, Graduate School of Science, The University of Osaka, Toyonaka, Osaka 560-0043, Japan

Funding

Japan Society for the Promotion of Science Award: JP23K26705

Shorai Foundation for Science and Technology

Ogasawara Foundation for the Promotion of Science and Engineering

Cite This Article

Naoya Kanbayashi, Kiyotaka Onitsuka (2026). Synthesis of optically active polymers containing a main-chain hydroxamic acid backbone via asymmetric polymerization. Polymer Chemistry. https://doi.org/10.1039/d6py00186f

Synthesis of optically active polymers containing a main-chain hydroxamic acid backbone via asymmetric polymerization

You May Also Like