Sustainable synthesis of CO2-derived polycarbonates from d-xylose
Literature Information
David K. Tran, Ahmed Z. Rashad, Donald J. Darensbourg
Synthetic transformation of D-xylose into a four-membered cyclic ether allows for reactions with carbon dioxide (CO2) leading to linear polycarbonates by either a one-step ring-opening copolymerisation (ROCOP) directly, or by sequential isolation of a preformed six-membered cyclic carbonate followed by ring-opening polymerisation (ROP).
Related Literature
Multilayer sensing platform: gold nanoparticles/prussian blue decorated graphite paper for NADH and H2O2 detection
Meng Wang, Xianwen Kan
DOI: 10.1039/C8AN01502C
Infrared spectral histopathology using haematoxylin and eosin (H&E) stained glass slides: a major step forward towards clinical translation
Michael J. Pilling, Alex Henderson, Jonathan H. Shanks, Michael D. Brown, Noel W. Clarke, Peter Gardner
DOI: 10.1039/C6AN02224C
Simple construction of ratiometric fluorescent probe for the detection of dopamine and tyrosinase by the naked eye
Guobin Mao, Mingyuan Du, Xinxin Wang, Xinghu Ji, Zhike He
DOI: 10.1039/C8AN01640B
Nicotinamide adenine dinucleotide detection based on silver nanoclusters stabilized by a dumbbell-shaped probe
Hong-Ya Wang, Jin-Liang Ma, Bin-Cheng Yin
DOI: 10.1039/C7AN00293A
Virtual staining of colon cancer tissue by label-free Raman micro-spectroscopy
D. Petersen, L. Mavarani, D. Niedieker, E. Freier, A. Tannapfel, C. Kötting, K. Gerwert, S. F. El-Mashtoly
DOI: 10.1039/C6AN02072K
Dicarboxylic acids as pH sensors for hyperpolarized 13C magnetic resonance spectroscopic imaging
C. Taglang, C. von Morze, J. E. Blecha, J. W. Gordon, R. Sriram, D. B. Vigneron, H. F. VanBrocklin, D. M. Wilson, R. R. Flavell
DOI: 10.1039/C7AN00076F
Optical properties of porcine dermis in the mid-infrared absorption band of glucose
Arthur Schönhals, Hans Tholl, Mathias Glasmacher, Niels Kröger-Lui, Annemarie Pucci, Wolfgang Petrich
DOI: 10.1039/C6AN01757F
Optimal voltage for nanoparticle detection with thin nanopores
DOI: 10.1039/C8AN01270A
Detection of Escherichia coli bacteria by impact electrochemistry
Rosa A. S. Couto, Lifu Chen, Sabine Kuss, Richard G. Compton
DOI: 10.1039/C8AN01675E
You might also like
What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?
N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...
What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?
When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...
What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?
Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...
What is the market or research trend for oxocopper (CAS: 12053-18-8)?
The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...
What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?
The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...
What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?
2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...
What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?
2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...
How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?
(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...
What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?
3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...
How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?
Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...
Source Journal
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.











![(2R,6S)-6-[(Benzyloxy)methyl]-4-{[(2-methyl-2-propanyl)oxy]carbonyl}-2-morpholinecarboxylic acid structure (2R,6S)-6-[(Benzyloxy)methyl]-4-{[(2-methyl-2-propanyl)oxy]carbonyl}-2-morpholinecarboxylic acid structure](https://static.chemtradehub.com/structs/109/1093085-91-6-3382.webp)
![1-{3-[4-Amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]-1-piperidinyl}-2,3-dihydroxy-1-propanone structure 1-{3-[4-Amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]-1-piperidinyl}-2,3-dihydroxy-1-propanone structure](https://static.chemtradehub.com/structs/122/1226872-27-0-e037.webp)

