Gradient isoselective ring-opening polymerization of racemic cyclic diolide driven by chiral phosphoric acid catalysis
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[1] M. Zaky,et al. Reaching High Stereoselectivity and Activity in Organocatalyzed Ring-Opening Polymerization of Racemic Lactide by the Combined Use of a Chiral (Thio)Urea and a N-Heterocyclic Carbene. , 2022, ACS macro letters.
[2] B. Tang,et al. Cobalt-Mediated Switchable Catalysis for One-Pot Synthesis of Cyclic Polymers. , 2021, Angewandte Chemie.
[3] Fosong Wang,et al. On-Demand Transformation of Carbon Dioxide into Polymers Enabled by Comb Shaped Metallic Oligomer Catalyst , 2021, ACS Catalysis.
[4] Y. Tao,et al. Synthesis of Sustainable Polyesters via Organocatalytic Ring-Opening Polymerization of O-carboxyanhydrides: Advances and Perspectives. , 2020, Macromolecular rapid communications.
[5] Jie Li,et al. Enantioselective terpolymerization of racemic and meso-epoxides with anhydrides for preparation of chiral polyesters , 2020, Proceedings of the National Academy of Sciences.
[6] L. Cavallo,et al. Biodegradable Polyhydroxyalkanoates by Stereoselective Copolymerization of Racemic Diolides: Stereocontrol Mechanism and Polyolefin-Like Properties. , 2020, Angewandte Chemie.
[7] E. Chen,et al. Stereosequenced crystalline polyhydroxyalkanoates from diastereomeric monomer mixtures , 2019, Science.
[8] D. Taton,et al. Isoselective Ring-Opening Polymerization of rac-Lactide from Chiral Takemoto's Organocatalysts: Elucidation of Stereocontrol. , 2018, ACS macro letters.
[9] Jianwei Sun,et al. Triflimide (HNTf2) in Organic Synthesis. , 2018, Chemical reviews.
[10] E. Chen,et al. Chemical synthesis of perfectly isotactic and high melting bacterial poly(3-hydroxybutyrate) from bio-sourced racemic cyclic diolide , 2018, Nature Communications.
[11] Zhibo Li,et al. Stereoselective Ring-Opening Polymerization of rac-Lactide Using Organocatalytic Cyclic Trimeric Phosphazene Base. , 2018, ACS macro letters.
[12] H. Sardón,et al. Enantioselective Ring-Opening Polymerization of rac-Lactide Dictated by Densely Substituted Amino Acids. , 2017, Journal of the American Chemical Society.
[13] G. Coates,et al. Ring-Opening Copolymerization of Epoxides and Cyclic Anhydrides with Discrete Metal Complexes: Structure-Property Relationships. , 2016, Chemical reviews.
[14] H. Sardón,et al. Update and challenges in organo-mediated polymerization reactions , 2016 .
[15] E. Chen,et al. From meso-Lactide to Isotactic Polylactide: Epimerization by B/N Lewis Pairs and Kinetic Resolution by Organic Catalysts. , 2015, Journal of the American Chemical Society.
[16] I. Goldberg,et al. Gradient isotactic multiblock polylactides from aluminum complexes of chiral salalen ligands. , 2014, Journal of the American Chemical Society.
[17] Joan Vignolle,et al. N-Heterocyclic carbenes (NHCs) as organocatalysts and structural components in metal-free polymer synthesis. , 2013, Chemical Society reviews.
[18] E. Jacobsen,et al. Asymmetric ion-pairing catalysis. , 2013, Angewandte Chemie.
[19] S. Grimme,et al. A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu. , 2010, The Journal of chemical physics.
[20] Eun Ji Shin,et al. Organocatalysis: Opportunities and Challenges for Polymer Synthesis , 2010 .
[21] C. Cramer,et al. Universal solvation model based on solute electron density and on a continuum model of the solvent defined by the bulk dielectric constant and atomic surface tensions. , 2009, The journal of physical chemistry. B.
[22] P. Schreiner,et al. (Thio)urea organocatalysis--what can be learnt from anion recognition? , 2009, Chemical Society reviews.
[23] Jamie M. Messman,et al. Organocatalytic stereoselective ring-opening polymerization of lactide with dimeric phosphazene bases. , 2007, Journal of the American Chemical Society.
[24] Stefan Grimme,et al. Semiempirical GGA‐type density functional constructed with a long‐range dispersion correction , 2006, J. Comput. Chem..
[25] J. Hedrick,et al. Stereoselective polymerization of rac- and meso-lactide catalyzed by sterically encumbered N-heterocyclic carbenes. , 2006, Chemical communications.
[26] P. Dalko,et al. In the golden age of organocatalysis. , 2004, Angewandte Chemie.
[27] Stefan Grimme,et al. Accurate description of van der Waals complexes by density functional theory including empirical corrections , 2004, J. Comput. Chem..
[28] Thomas Frauenheim,et al. Hydrogen bonding and stacking interactions of nucleic acid base pairs: A density-functional-theory based treatment , 2001 .
[29] M. Frisch,et al. Ab Initio Calculation of Vibrational Absorption and Circular Dichroism Spectra Using Density Functional Force Fields , 1994 .
[30] A. Becke. Density-functional thermochemistry. III. The role of exact exchange , 1993 .
[31] H. Bernhard Schlegel,et al. Reaction Path Following in Mass-Weighted Internal Coordinates , 1990 .
[32] David Feller,et al. Basis Set Selection for Molecular Calculations , 1986 .
[33] K. Fukui. The path of chemical reactions - the IRC approach , 1981 .
[34] A. Schindler,et al. Poly (lactic acid). I. Stereosequence distribution in the polymerization of racemic dilactide , 1976 .
[35] B. List,et al. IDPi Catalysis. , 2019, Angewandte Chemie.