Synthesis of a novel crown ether derived from chiro-inositol and its catalytic activity on the asymmetric Michael addition
Literature Information
Takahiko Akiyama, Mikiko Hara, Kohei Fuchibe, Shigeru Sakamoto, Kentaro Yamaguchi
A novel 18-membered chiral crown ether was prepared in four steps starting from L-quebrachitol, a chiro-inositol, and its catalytic activity in the Michael addition reaction of glycine imine with several Michael acceptors was studied.
Recommended Journals
Related Literature
Transition of interfacial capacitors in electrowetting on a graphite surface by ion intercalation
DOI: 10.1039/C9CP04436A
Mn 2p resonant X-ray emission clarifies the redox reaction and charge-transfer effects in LiMn2O4
Yusuke Nanba, Masashi Okubo, Hisao Kiuchi
DOI: 10.1039/C9CP02604E
The dual-defective SnS2 monolayers: promising 2D photocatalysts for overall water splitting
DOI: 10.1039/C9CP04649F
High thermoelectric performance of Ag doped SnTe polycrystalline bulks via the synergistic manipulation of electrical and thermal transport
Jun Wang, Jichao Li, Jian Liu, Chunlei Wang, Jiyang Wang, Xiaolin Wang
DOI: 10.1039/C9CP03534F
Using photoelectron spectroscopy to observe oxygen spillover to zirconia
Peter Lackner, Zhiyu Zou, Sabrina Mayr, Ulrike Diebold, Michael Schmid
DOI: 10.1039/C9CP03322J
Theoretical insights into the effect of the overpotential on CO electroreduction mechanisms on Cu(111): regulation and application of electrode potentials from a CO coverage-dependent electrochemical model
Lihui Ou, Junxiang Chen
DOI: 10.1039/C9CP05043D
High-throughput HSE study on the doping effect in anatase TiO2
Jiahua Liu, Mouyi Weng, Sibai Li, Xin Chen, Jianhang Cen, Jianshu Jie, Weiji Xiao, Jiaxin Zheng, Feng Pan
DOI: 10.1039/C9CP04591K
Enhanced VOC of two-dimensional Ruddlesden–Popper perovskite solar cells using binary synergetic organic spacer cations
Di Huang, Haina Zhu
DOI: 10.1039/C9CP04018H
Solvation dynamics: improved reproduction of the time-dependent Stokes shift with polarizable empirical force field chromophore models
Stella Schmode, Payal Chatterjee, Alexander D. MacKerell, Jr., Christian Schröder
DOI: 10.1039/C9CP03000J
You might also like
What precautions should be taken when handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3)?
When handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3), safety go...
What is 4-(3,5-Difluorophenyl)aniline (CAS: 405058-00-6)?
4-(3,5-Difluorophenyl)aniline is an aromatic organic compound with the CAS numbe...
How is 5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid (CAS: 338982-07-3) typically synthesized?
5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid can ...
What is the market or research trend for 4-Benzylaniline hydrochloride (CAS: 6317-57-3)?
The market for 4-Benzylaniline hydrochloride (CAS: 6317-57-3) is steadily growin...
Is [3-(Diethylsulfamoyl)phenyl]boronic acid (CAS: 871329-58-7) safe?
[3-(Diethylsulfamoyl)phenyl]boronic acid is generally considered safe when handl...
What are the main uses of 3-Bromo-2,5-dimethoxyaniline (CAS: 115929-62-9)?
3-Bromo-2,5-dimethoxyaniline is mainly used in the pharmaceutical and chemical i...
What regulatory guidelines apply to N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7)?
N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7) is subject to ...
What industries use Carbamic acid, N-[(5S)-5,6-diamino-6-oxohexyl]-, 1,1-dimethylethyl ester (CAS: 24828-96-4)?
This compound is primarily used in the pharmaceutical industry for the synthesis...
How should 2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) be stored?
2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) sho...
What industries use Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9)?
Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9) is utilized in the pharma...
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














