Manipulation of the stereochemical outcome and product distribution in the Henry reaction using CO2 pressure

Literature Information

Publication Date 2004-10-08
DOI 10.1039/B409451D
Impact Factor 6.222
Authors

Andrew J. Parratt, Dave J. Adams, Anthony A. Clifford, Christopher M. Rayner


View Original

Abstract

The rate and stereocontrol of the Henry reaction in the presence of CO2 can be controlled simply by manipulation of CO2 pressure, and can be understood by consideration of the kinetic and thermodynamic aspects of the reaction.

Related Literature

Back cover

Cover

DOI: 10.1039/D0SE90044C

An auxiliary electrode mediated membrane-free redox electrochemical cell for energy storage

Senthil Velan Venkatesan, Kunal Karan, Stephen R. Larter, Venkataraman Thangadurai

2019-11-11 Communication

DOI: 10.1039/C9SE00734B

A safe Li–Se battery in an ionic liquid-based electrolyte operating at 25–70 °C by using a N,S,O tri-doped mesoporous carbon host material

Cuong Nguyen, Anders J. Barlow, Pavel V. Cherepanov, Maria Forsyth, Patrick C. Howlett, Douglas R. MacFarlane

2020-02-27 Paper

DOI: 10.1039/C9SE01074B

Back cover

2021-06-04 Cover

DOI: 10.1039/D1BM90057A

Inside back cover

Cover

DOI: 10.1039/D0SE90043E

Glucose-sensitive nanofiber scaffolds with an improved sensing design for physiological conditions

Mary K. Balaconis, Yi Luo, Heather A. Clark

2014-11-26 Paper

DOI: 10.1039/C4AN01775G

Fuel cell evaluation of anion exchange membranes based on poly(phenylene oxide) with different cationic group placement

Annika Carlson, Björn Eriksson, Joel S. Olsson, Göran Lindbergh, Carina Lagergren, Patric Jannasch, Rakel Wreland Lindström

2020-02-24 Paper

DOI: 10.1039/C9SE01143A

Chemically diverse polymer microarrays and high throughput surface characterisation: a method for discovery of materials for stem cell culture

A. D. Celiz, J. G. W. Smith, A. K. Patel, R. Langer, D. G. Anderson, D. A. Barrett, L. E. Young, M. C. Davies, C. Denning, M. R. Alexander

2014-05-12 Communication

DOI: 10.1039/C4BM00054D

Dual-stage growth factor release within 3D protein-engineered hydrogel niches promotes adipogenesis

Midori Greenwood-Goodwin, Eric S. Teasley

2014-08-07 Paper

DOI: 10.1039/C4BM00142G

You might also like

Compound Q&A

What industries use 4-(4-tert-Butylphenyl)-1H-pyrazol-3-amine (CAS: 1015845-73-4)?

4-(4-tert-Butylphenyl)-1H-pyrazol-3-amine finds applications in various industri...

1015845-73-44-(4-tert-Butylpheny...
Compound Q&A

What industries use H3TATAB (CAS: 63557-10-8)?

H3TATAB is used in the pharmaceutical industry for the synthesis of certain orga...

63557-10-8H3TATAB
Compound Q&A

What are the main uses of 1-Ethyl-3-fluorobenzene (CAS: 696-39-9)?

1-Ethyl-3-fluorobenzene (CAS: 696-39-9) is primarily used as a precursor in the ...

696-39-91-Ethyl-3-fluorobenz...
Compound Q&A

What are the main uses of 1-(tert-Butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylic acid (CAS: 851484-94-1)?

1-(tert-Butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylic acid is prim...

851484-94-11-(tert-Butoxycarbon...
Compound Q&A

What are the physical and chemical properties of 1-Cyclobutyl-4-piperidinone (CAS: 359880-05-0)?

1-Cyclobutyl-4-piperidinone (CAS: 359880-05-0) is a colorless or white crystalli...

359880-05-01-Cyclobutyl-4-piper...
Compound Q&A

What is Pyridine-2,6-dicarboxylic acid mono-tert-butyl ester (CAS: 575433-76-0)?

Pyridine-2,6-dicarboxylic acid mono-tert-butyl ester (CAS: 575433-76-0) is a che...

575433-76-0Pyridine-2,6-dicarbo...
Compound Q&A

What is the market or research trend for 2,3-Difluorophenylalanine (CAS: 236754-62-4)?

The market for 2,3-Difluorophenylalanine (CAS: 236754-62-4) is growing with incr...

236754-62-42,3-Difluorophenylal...
Compound Q&A

How is (2-Hydroxy-1-naphthyl)boronic acid (CAS: 898257-48-2) typically synthesized?

(2-Hydroxy-1-naphthyl)boronic acid can be synthesized through the reduction of 2...

898257-48-2(2-Hydroxy-1-naphthy...
1315351-28-0tert-Butyl (5-bromo-...
Compound Q&A

Are there alternatives to 5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl beta-D-glucopyranoside (CAS: 19833-12-6) in synthesis?

While 5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl beta-D-gluc...

19833-12-65,7-Dihydroxy-4-oxo-...

Source Journal

Chemical Communications

Chemical Communications
CiteScore: 8.6
Self-citation Rate: 4.7%
Articles per Year: 2458

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

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.