Ring-Opening Polymerization of Lactides Catalyzed by Natural Amino-Acid Based Zinc Catalysts

Donald J. Darensbourg; Osit Karroonnirun

doi:10.1021/ic902271x

Ring-Opening Polymerization of Lactides Catalyzed by Natural Amino-Acid Based Zinc Catalysts

Inorganic Chemistry ◽

10.1021/ic902271x ◽

2010 ◽

Vol 49 (5) ◽

pp. 2360-2371 ◽

Cited By ~ 156

Author(s):

Donald J. Darensbourg ◽

Osit Karroonnirun

Keyword(s):

Amino Acid ◽

Ring Opening ◽

Ring Opening Polymerization ◽

Natural Amino Acid

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Effect and regulation of the secondary structure of synthetic poly(α-amino acid) based on ring-opening polymerization

Chinese Science Bulletin (Chinese Version) ◽

10.1360/tb-2020-1114 ◽

2020 ◽

Author(s):

成龙 Ge ◽

勇 Liu ◽

黎晨 Yin

Keyword(s):

Amino Acid ◽

Secondary Structure ◽

Ring Opening ◽

Ring Opening Polymerization ◽

Alpha Amino Acid

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Ring-Opening Polymerization of Amino Acid N-Carboxyanhydrides

Polymer Science: A Comprehensive Reference ◽

10.1016/b978-0-444-53349-4.00111-4 ◽

2012 ◽

pp. 427-449 ◽

Cited By ~ 2

Author(s):

T.J. Deming

Keyword(s):

Amino Acid ◽

Ring Opening ◽

Ring Opening Polymerization

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Ring opening polymerization of α-amino acid N-carboxyanhydrides catalyzed by rare earth catalysts: Polymerization characteristics and mechanism

Journal of Polymer Science Part A Polymer Chemistry ◽

10.1002/pola.25848 ◽

2011 ◽

Vol 50 (6) ◽

pp. 1076-1085 ◽

Cited By ~ 36

Author(s):

Hui Peng ◽

Jun Ling ◽

Zhiquan Shen

Keyword(s):

Rare Earth ◽

Amino Acid ◽

Ring Opening ◽

Ring Opening Polymerization

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Fast and Living Ring-Opening Polymerization of α-Amino Acid N-Carboxyanhydrides Triggered by an “Alliance” of Primary and Secondary Amines at Room Temperature

Biomacromolecules ◽

10.1021/acs.biomac.5b00134 ◽

2015 ◽

Vol 16 (4) ◽

pp. 1352-1357 ◽

Cited By ~ 34

Author(s):

Wei Zhao ◽

Yves Gnanou ◽

Nikos Hadjichristidis

Keyword(s):

Amino Acid ◽

Ring Opening ◽

Room Temperature ◽

Ring Opening Polymerization ◽

Secondary Amines ◽

Primary And Secondary Amines

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Random Poly(Amino Acid)s Synthesized by Ring Opening Polymerization as Additives in the Biomimetic Mineralization of CaCO3

Polymers ◽

10.3390/polym4021195 ◽

2012 ◽

Vol 4 (2) ◽

pp. 1195-1210 ◽

Cited By ~ 18

Author(s):

Vladimir Dmitrovic ◽

Gijs J.M. Habraken ◽

Marco M.R.M. Hendrix ◽

Wouter J.E.M. Habraken ◽

Andreas Heise ◽

...

Keyword(s):

Amino Acid ◽

Ring Opening ◽

Ring Opening Polymerization ◽

Biomimetic Mineralization

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Organobase 1,1,3,3-Tetramethyl Guanidine Catalyzed Rapid Ring-opening Polymerization of α-Amino Acid N-carboxyanhydrides Adaptive to Amine, Alcohol and Carboxyl Acid Initiators

Polymer Chemistry ◽

10.1039/d1py01508g ◽

2021 ◽

Author(s):

Kai Li ◽

Zheng Li ◽

Yong Shen ◽

Xiaohui Fu ◽

Chongyi Chen ◽

...

Keyword(s):

Amino Acid ◽

Ring Opening ◽

Ring Opening Polymerization

The initiators for ring-opening polymerization (ROP) of α-amino acid N-carboxyanhydrides (NCA) to prepare polypeptides usually require high nucleophilicity. For the initiators with lower nucleophilicity, slow initiation and fast propagation lead...

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Synthesis of Glycopeptide-conjugates via Ring-opening Polymerization of Sugar-substituted .ALPHA.-Amino Acid N-Carboxyanhydrides (GlycoNCAs).

Proceedings of the Japan Academy Series B ◽

10.2183/pjab.73.205 ◽

1997 ◽

Vol 73 (10) ◽

pp. 205-209 ◽

Cited By ~ 7

Author(s):

Masahiko OKADA ◽

Keigo AOI ◽

Kaname TSUTSUMIUCHI

Keyword(s):

Amino Acid ◽

Ring Opening ◽

Ring Opening Polymerization ◽

Alpha Amino Acid

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Investigation of α-amino acid N-carboxyanhydrides by X-ray diffraction for controlled ring-opening polymerization

Tetrahedron Letters ◽

10.1016/j.tetlet.2018.12.028 ◽

2019 ◽

Vol 60 (3) ◽

pp. 272-275 ◽

Cited By ~ 2

Author(s):

Olga Schäfer ◽

Dieter Schollmeyer ◽

Alexander Birke ◽

Regina Holm ◽

Kerstin Johann ◽

...

Keyword(s):

Amino Acid ◽

Ring Opening ◽

Ring Opening Polymerization ◽

X Ray Diffraction ◽

X Ray

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Glycopeptide Synthesis by an .alpha.-Amino Acid N-Carboxyanhydride (NCA) Method: Ring-Opening Polymerization of a Sugar-Substituted NCA

Macromolecules ◽

10.1021/ma00081a040 ◽

1994 ◽

Vol 27 (3) ◽

pp. 875-877 ◽

Cited By ~ 92

Author(s):

Keigo Aoi ◽

Kaname Tsutsumiuchi ◽

Masahiko Okada

Keyword(s):

Amino Acid ◽

Ring Opening ◽

Ring Opening Polymerization ◽

Alpha Amino Acid

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Controlled ring-opening polymerization of α-amino acid N-carboxy-anhydride by frustrated amine/borane Lewis pairs

Chemical Communications ◽

10.1039/c7cc01440f ◽

2017 ◽

Vol 53 (37) ◽

pp. 5155-5158 ◽

Cited By ~ 29

Author(s):

Hongyuan Zhang ◽

Yanzhao Nie ◽

Xinmei Zhi ◽

Haifeng Du ◽

Jing Yang

Keyword(s):

Amino Acid ◽

Lewis Acid ◽

Ring Opening ◽

Ring Opening Polymerization ◽

Amine Groups ◽

Lewis Pairs

An FLP intermediate formed through the bulky borane Lewis acid and the amine groups of the propagation chain end controlled the ring-opening polymerization of α-amino acid N-carboxy-anhydride monomers.

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