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Literature DB >> 18604787

A simple, rapid method for the preparation of [11C]formaldehyde.

Jacob M Hooker¹, Matthias Schönberger, Hanno Schieferstein, Joanna S Fowler.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 2008 PMID： 18604787 PMCID： PMC2522306 DOI： 10.1002/anie.200800991

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

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12 in total

1. The preparation of 11C-methyl iodide and its use in the synthesis of 11C-methyl-L-methionine.

Authors: B Långström; H Lundqvist
Journal: Int J Appl Radiat Isot Date: 1976-07

2. Detection of DNA synthesis in intact organisms with positron-emitting (methyl- 11 C)thymidine.

Authors: D Christman; E J Crawford; M Friedkin; A P Wolf
Journal: Proc Natl Acad Sci U S A Date: 1972-04 Impact factor: 11.205

3. Synthesis of methyl iodide-11 C and formaldehyde-11 C.

Authors: C Marazano; M Maziere; G Berger; D Comar
Journal: Int J Appl Radiat Isot Date: 1977 Jan-Feb

4. Enzymatic synthesis of C-11 formaldehyde: concise communication.

Authors: G Slegers; R H Lambrecht; T Vandewalle; L Meulewaeter; C Vandecasteele
Journal: J Nucl Med Date: 1984-03 Impact factor: 10.057

5. Automated synthesis of 11C-labelled radiopharmaceuticals: imipramine, chlorpromazine, nicotine and methionine.

Authors: G Berger; M Maziere; R Knipper; C Prenant; D Comar
Journal: Int J Appl Radiat Isot Date: 1979-07

6. A general method for labeling proteins with 11C.

Authors: M G Straatmann; M J Welch
Journal: J Nucl Med Date: 1975-05 Impact factor: 10.057

7. Positron emission tomography provides molecular imaging of biological processes.

Authors: M E Phelps
Journal: Proc Natl Acad Sci U S A Date: 2000-08-01 Impact factor: 11.205

8. Semi-automated preparation of a 11C-labelled antibiotic--[N-methyl-11C]erythromycin A lactobionate.

Authors: V W Pike; A J Palmer; P L Horlock; T J Perun; L A Freiberg; D A Dunnigan; R H Liss
Journal: Int J Appl Radiat Isot Date: 1984-02

9. Carbon 11 labeling of the psychoactive drug o-methyl-bufotenine and its distribution in the animal organism.

Authors: G Berger; M Mazière; C Marazano; D Comar
Journal: Eur J Nucl Med Date: 1978-04-01

10. Preparation of [11C]formaldehyde using a hollow fiber membrane bioreactor.

Authors: J A Hughes; M Jay
Journal: Nucl Med Biol Date: 1995-01 Impact factor: 2.408

16 in total

1. A fast chemoenzymatic synthesis of [11C]-N5,N10-methylenetetrahydrofolate as a potential PET tracer for proliferating cells.

Authors: Muhammad Saeed; Timothy J Tewson; Colbin E Erdahl; Amnon Kohen
Journal: Nucl Med Biol Date: 2012-02-01 Impact factor: 2.408

2. Novel positron emission tomography tracer distinguishes normal from cancerous cells.

Authors: Muhammad Saeed; David Sheff; Amnon Kohen
Journal: J Biol Chem Date: 2011-08-08 Impact factor: 5.157

Review 3. Modular strategies for PET imaging agents.

Authors: Jacob M Hooker
Journal: Curr Opin Chem Biol Date: 2009-10-31 Impact factor: 8.822

Review 4. Considerations in the Development of Reversibly Binding PET Radioligands for Brain Imaging.

Authors: Victor W Pike
Journal: Curr Med Chem Date: 2016 Impact factor: 4.530

Review 5. (11)C[double bond, length as m-dash]O bonds made easily for positron emission tomography radiopharmaceuticals.

Authors: Benjamin H Rotstein; Steven H Liang; Michael S Placzek; Jacob M Hooker; Antony D Gee; Frédéric Dollé; Alan A Wilson; Neil Vasdev
Journal: Chem Soc Rev Date: 2016-08-22 Impact factor: 54.564

Review 6. Chemistry for Positron Emission Tomography: Recent Advances in ¹¹ C-, ¹⁸ F-, ¹³ N-, and ¹⁵ O-Labeling Reactions.

Authors: Xiaoyun Deng; Jian Rong; Lu Wang; Neil Vasdev; Lei Zhang; Lee Josephson; Steven H Liang
Journal: Angew Chem Int Ed Engl Date: 2019-01-14 Impact factor: 15.336

A simple, rapid method for the preparation of [11C]formaldehyde.

1. The preparation of 11C-methyl iodide and its use in the synthesis of 11C-methyl-L-methionine.

2. Detection of DNA synthesis in intact organisms with positron-emitting (methyl- 11 C)thymidine.

3. Synthesis of methyl iodide-11 C and formaldehyde-11 C.

4. Enzymatic synthesis of C-11 formaldehyde: concise communication.

5. Automated synthesis of 11C-labelled radiopharmaceuticals: imipramine, chlorpromazine, nicotine and methionine.

6. A general method for labeling proteins with 11C.

7. Positron emission tomography provides molecular imaging of biological processes.

8. Semi-automated preparation of a 11C-labelled antibiotic--[N-methyl-11C]erythromycin A lactobionate.

9. Carbon 11 labeling of the psychoactive drug o-methyl-bufotenine and its distribution in the animal organism.

10. Preparation of [11C]formaldehyde using a hollow fiber membrane bioreactor.

1. A fast chemoenzymatic synthesis of [11C]-N5,N10-methylenetetrahydrofolate as a potential PET tracer for proliferating cells.

2. Novel positron emission tomography tracer distinguishes normal from cancerous cells.

Review 3. Modular strategies for PET imaging agents.

Review 4. Considerations in the Development of Reversibly Binding PET Radioligands for Brain Imaging.

Review 5. (11)C[double bond, length as m-dash]O bonds made easily for positron emission tomography radiopharmaceuticals.

Review 6. Chemistry for Positron Emission Tomography: Recent Advances in ¹¹ C-, ¹⁸ F-, ¹³ N-, and ¹⁵ O-Labeling Reactions.

7. [¹¹C]Cyanation of arylboronic acids in aqueous solutions.

8. Radionuclide labeling and evaluation of candidate radioligands for PET imaging of histone deacetylase in the brain.

9. Synthesis and evaluation of methylated arylazepine compounds for PET imaging of 5-HT(2c) receptors.

10. One-pot, direct incorporation of [11C]CO2 into carbamates.

Review 3. Modular strategies for PET imaging agents.

Review 4. Considerations in the Development of Reversibly Binding PET Radioligands for Brain Imaging.

Review 5. (11)C[double bond, length as m-dash]O bonds made easily for positron emission tomography radiopharmaceuticals.

Review 6. Chemistry for Positron Emission Tomography: Recent Advances in 11 C-, 18 F-, 13 N-, and 15 O-Labeling Reactions.

Review 6. Chemistry for Positron Emission Tomography: Recent Advances in ¹¹ C-, ¹⁸ F-, ¹³ N-, and ¹⁵ O-Labeling Reactions.