Pictet–Spengler reactions in multiphasic supercritical carbon dioxide/CO2-expanded liquid media. In situ generation of carbamates as a strategy for reactions of amines in supercritical carbon dioxide
Literature Information
Joshua R. Dunetz, Rocco P. Ciccolini, Morgan Fröling, Scott M. Paap, Andrew J. Allen, Jefferson W. Tester, Rick L. Danheiser
Acyl-Pictet–Spengler cyclizations can be achieved in scCO2/CO2-expanded liquid media via the in situ formation of carbamate derivatives of β-arylethylamines.
Related Literature
Dehydrogenation of the liquid organic hydrogen carrier perhydrodibenzyltoluene – reaction pathway over Pt/Al2O3
Suitao Qi, Kevin J. Smith, Yiming Zhou
DOI: 10.1039/D2RE00345G
An environmentally benign and high-rate Appel type reaction
Nicolas Mattias Del Rio Fuenzalida, Eirin Alme, Frida Johanne Lundevall, Hans-René Bjørsvik
DOI: 10.1039/D2RE00071G
Room-temperature conversion of CO2 into quinazoline-2,4(1H,3H)-dione using deep eutectic solvents at atmospheric pressure with high efficiency
Yu Chen, Chong Liu, Yaoting Duan, Dongkun Yu, Zhenghui Liu, Yuting Li, Ruifen Shi, Yuting Guo, Tiancheng Mu
DOI: 10.1039/D2RE00137C
Enhanced flow synthesis of small molecules by in-line integration of sequential catalysis and benchtop twin-column continuous chromatography
Alessandra Sivo, Tae Keun Kim, Vincenzo Ruta, Renzo Luisi, Jose Osorio-Tejada, Marc Escriba-Gelonch, Volker Hessel, Mattia Sponchioni, Gianvito Vilé
DOI: 10.1039/D2RE00242F
Outstanding Reviewers for Reaction Chemistry & Engineering in 2021
DOI: 10.1039/D2RE90024F
Deamidation reaction network mapping of pharmacologic and related proteins: impact of solvation dielectric on the degradation energetics of asparagine dipeptides
Katherine E. Lawson, Joseph K. Dekle, Megan N. Evans, Andrew J. Adamczyk
DOI: 10.1039/D2RE00110A
Analysis of n-hexane, 1-hexene, cyclohexane and cyclohexene catalytic cracking over HZSM-5 zeolites: effects of molecular structure
Zhenzhou Ma, Bochong Chen, Liu Zhao, Enxian Yuan, Tingting Cui
DOI: 10.1039/D1RE00532D
The effect of MgO and preparation techniques of the FeMnOδ/MgO–Al2O3 catalyst used for the vapor phase oxidation of cyclohexane
Vijendra Kumar Yadav, Taraknath Das
DOI: 10.1039/D2RE00210H
Rapid optimisation of API crystallisation in a segmented flow reactor with a continuous, variable temperature gradient
DOI: 10.1039/D2RE00183G
You might also like
How should waste containing 2-Ethyl-4-Methyl-1H-Imidazole-5-Carbaldehyde (CAS: 88634-80-4) be handled?
Waste containing 2-Ethyl-4-Methyl-1H-Imidazole-5-Carbaldehyde (CAS: 88634-80-4) ...
What industries use Triethoxy(octyl)silane (CAS: 1385031-14-0)?
Triethoxy(octyl)silane (CAS: 1385031-14-0) is widely used in the pharmaceuticals...
Are there alternatives to 3-iodo-7-nitro-1H-indazole (CAS: 864724-64-1) in synthesis?
Several alternatives to 3-iodo-7-nitro-1H-indazole (CAS: 864724-64-1) exist in t...
Are there alternatives to Benzene, bis[(trimethoxysilyl)ethyl] (CAS: 266317-71-9) in synthesis?
Yes, there are alternatives to Benzene, bis[(trimethoxysilyl)ethyl] (CAS: 266317...
Is Isothiazole-3-carbonitrile (CAS: 1452-17-1) safe?
Isothiazole-3-carbonitrile (CAS: 1452-17-1) is generally considered safe when us...
Is (3-Chlorophenyl)methanol (CAS: 873-63-2) safe?
(3-Chlorophenyl)methanol (CAS: 873-63-2) is considered low to moderately toxic. ...
How is (2S,3S)-2-Hydroxy-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-3-(2-naphthyl)propanoic acid (CAS: 959583-98-3) typically synthesized?
(2S,3S)-2-Hydroxy-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-3-(2-naphthyl)pr...
What precautions should be taken when handling Methyl 2-(bromomethyl)-5-methoxybenzoate (CAS: 788081-99-2)?
Proper handling of methyl 2-(bromomethyl)-5-methoxybenzoate requires the use of ...
What is 6,8-Dibromoimidazo[1,2-a]pyridine-2-carboxylic acid (CAS: 904805-36-3)?
6,8-Dibromoimidazo[1,2-a]pyridine-2-carboxylic acid (CAS: 904805-36-3) is an aro...
Is 3-Amino-5-bromo-2-pyridinecarbonitrile (CAS: 573675-27-1) safe?
3-Amino-5-bromo-2-pyridinecarbonitrile is considered safe when handled under pro...
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










![N-[(5,6-Dichloro-1H-benzimidazol-2-yl)methyl]-9-(1-methyl-1H-pyrazol-4-yl)-2-(4-morpholinyl)-9H-purin-6-amine structure N-[(5,6-Dichloro-1H-benzimidazol-2-yl)methyl]-9-(1-methyl-1H-pyrazol-4-yl)-2-(4-morpholinyl)-9H-purin-6-amine structure](https://static.chemtradehub.com/structs/238/2387704-62-1-25f4.webp)
![N,N'-1,2-Ethanediylbis[2-(vinylsulfonyl)acetamide] structure N,N'-1,2-Ethanediylbis[2-(vinylsulfonyl)acetamide] structure](https://static.chemtradehub.com/structs/667/66710-66-5-b556.webp)


