In tube determination of the absolute configuration of α- and β-hydroxy acids by NMR via chiral BINOL borates
Literature Information
Félix Freire, Emilio Quiñoá, Ricardo Riguera
A simple NMR methodology, through the formation of chiral BINOL borates in the NMR tube, and that reunites the advantages of chiral derivatizing (CDAs) and chiral solvating agents (CSAs), is presented for the assignment of the absolute configuration of α- and β-hydroxy acids.
Related Literature
Two-dimensional carbon dioxide with high stability, a negative Poisson's ratio and a huge band gap
Guoling Li, Liben Li, Xingqiang Shi, Bingbing Liu
DOI: 10.1039/C8CP02742K
DFT investigation on the adsorption of munition compounds on α-Fe2O3: similarity and differences with α-Al2O3
Glen R. Jenness, Jennifer Seiter, Manoj K. Shukla
DOI: 10.1039/C8CP02590H
Detection and characterization at nM concentration of oligomers formed by hIAPP, Aβ(1–40) and their equimolar mixture using SERS and MD simulations
Luisa D’Urso, Marcello Condorelli, Orazio Puglisi, Carmelo Tempra, Giuseppe Compagnini, Carmelo La Rosa
DOI: 10.1039/C7CP08552D
Thermally induced carbonation of Ca(OH)2 in a CO2 atmosphere: kinetic simulation of overlapping mass-loss and mass-gain processes in a solid–gas system
Nobuyoshi Koga, Satoki Kodani
DOI: 10.1039/C8CP05701J
Excited state intramolecular proton transfer in julolidine derivatives: an ab initio study
Šimon Budzák, Denis Jacquemin
DOI: 10.1039/C8CP04356F
Arsenene nanoribbon edge-resolved strong magnetism
Xi Zhang, Yongli Huang, Chang Q. Sun
DOI: 10.1039/C8CP04891F
Suppression of surfaces states at cubic perovskite (001) surfaces by CO2 adsorption
Kostiantyn V. Sopiha, Oleksandr I. Malyi, Clas Persson, Ping Wu
DOI: 10.1039/C8CP02535E
Substrate-affected lattice structural evolution in compressed monolayer ReS2
Yalan Yan, Hao Liu, Yonghao Han, Fangfei Li, Chunxiao Gao
DOI: 10.1039/C8CP03701A
You might also like
What precautions should be taken when handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3)?
When handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3), it ...
What precautions should be taken when handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9)?
When handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9), it...
How should waste containing 2-[2-(2-Methoxyethoxy)ethoxy]ethyl 4-methylbenzenesulfonate (CAS: 62921-74-8) be handled?
Waste containing this compound (CAS: 62921-74-8) should be handled according to ...
How should waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate be handled?
Waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate should be collected i...
How is 5-({4-[(2S,4R)-4-Hydroxy-2-methyltetrahydro-2H-pyran-4-yl]-2-thienyl}sulfanyl)-1-methyl-1,3-dihydro-2H-indol-2-one (CAS: 166882-70-8) typically synthesized?
This compound can be synthesized using a multi-step process involving the conjug...
Are there alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid (CAS: 7312-27-8) in synthesis?
There are several alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid in syn...
How should Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84-9) be stored?
Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84...
How should waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) be handled?
Waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) should be coll...
How is Methyl 5-iodo-2-methylbenzoate (CAS: 103440-54-6) typically synthesized?
Methyl 5-iodo-2-methylbenzoate can be synthesized through the iodination of meth...
How is 5-Chloro[1,2,4]triazolo[1,5-a]pyridine (CAS: 1427399-34-5) typically synthesized?
5-Chloro[1,2,4]triazolo[1,5-a]pyridine is commonly synthesized via the condensat...
Source Journal
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry










![[4-(Heptyloxy)phenyl]boronic acid structure [4-(Heptyloxy)phenyl]boronic acid structure](https://static.chemtradehub.com/structs/136/136370-19-9-ad33.webp)



