Publications
Selected publications
- Development of the esterase PestE for amide bond synthesis under aqueous conditions: Enzyme cascades for converting waste PET into tamibarotene. (Journal article - 2024)
- Engineering a Carboxyl Methyltransferase for the Formation of a Furan-Based Bioplastic Precursor (Journal article - 2023)
- Carboxyl Methyltransferase Catalysed Formation of Mono‐ and Dimethyl Esters under Aqueous Conditions: Application in Cascade Biocatalysis (Journal article - 2022)
- Carboxyl Methyltransferases: Natural Functions and Potential Applications in Industrial Biotechnology (Journal article - 2021)
- PET hydrolysing enzymes catalyse bioplastics precursor synthesis under aqueous conditions (Journal article - 2019)
- The continuous oxidation of HMF to FDCA and the immobilisation and stabilisation of periplasmic aldehyde oxidase (PaoABC) (Journal article - 2017)
- Real‐Time Monitoring of Enzyme‐Catalysed Reactions using Deep UV Resonance Raman Spectroscopy (Journal article - 2017)
- Enzyme cascade reactions: synthesis of furandicarboxylic acid (FDCA) and carboxylic acids using oxidases in tandem (Journal article - 2015)
- Chemoenzymatic Synthesis and Application of Bicyclo[2.2.2]octadiene Ligands: Increased Efficiency in Rhodium-Catalyzed Asymmetric Conjugate Additions by Electronic Tuning (Journal article - 2010)
- Carboxyl Methyltransferase Catalysed Formation of Mono- and Dimethyl Esters under Aqueous Conditions: Application in Cascade Biocatalysis (Journal article - 2022)
2024
Development of the esterase PestE for amide bond synthesis under aqueous conditions: Enzyme cascades for converting waste PET into tamibarotene.
Goulding, E., Ward, L., Allan, F., Dittman, D., Salcedo-Sora, J. E., & Carnell, A. J. (2024). Development of the esterase PestE for amide bond synthesis under aqueous conditions: Enzyme cascades for converting waste PET into tamibarotene.. Angewandte Chemie (International ed. in English), e202414162. doi:10.1002/anie.202414162
Development of the esterase PestE for amide bond synthesis under aqueous conditions: Enzyme cascades for converting waste PET into tamibarotene.
Goulding, E., Ward, L., Allan, F., Dittman, D., Salcedo-Sora, J. E., & Carnell, A. J. (n.d.). Development of the esterase PestE for amide bond synthesis under aqueous conditions: Enzyme cascades for converting waste PET into tamibarotene.. Angewandte Chemie. doi:10.1002/ange.202414162
Rational design of a cyclohexanone dehydrogenase for enhanced α,β-desaturation and substrate specificity.
Singh, W., Brown, N. L., McCue, H. V., Marriott, S. R., Wilson, R. C., Perry, J., . . . Black, G. W. (2024). Rational design of a cyclohexanone dehydrogenase for enhanced α,β-desaturation and substrate specificity.. Chemical science, 15(13), 4969-4980. doi:10.1039/d3sc04009g
2023
Engineering a Carboxyl Methyltransferase for the Formation of a Furan-Based Bioplastic Precursor
Ward, L. C., Goulding, E., Rigden, D. J., Allan, F. E., Pellis, A., Hatton, H., . . . Carnell, A. J. (2023). Engineering a Carboxyl Methyltransferase for the Formation of a Furan-Based Bioplastic Precursor. CHEMSUSCHEM. doi:10.1002/cssc.202300516
Targeted Destruction of S100A4 Inhibits Metastasis of Triple Negative Breast Cancer Cells
Ismail, T. M., Crick, R. G., Du, M., Shivkumar, U., Carnell, A., Barraclough, R., . . . Rudland, P. S. (2023). Targeted Destruction of S100A4 Inhibits Metastasis of Triple Negative Breast Cancer Cells. BIOMOLECULES, 13(7). doi:10.3390/biom13071099
2022
Carboxyl Methyltransferase Catalysed Formation of Mono- and Dimethyl Esters under Aqueous Conditions: Application in Cascade Biocatalysis
Ward, L. C., McCue, H. V., Rigden, D. J., Kershaw, N. M., Ashbrook, C., Hatton, H., . . . Carnell, A. J. (2022). Carboxyl Methyltransferase Catalysed Formation of Mono- and Dimethyl Esters under Aqueous Conditions: Application in Cascade Biocatalysis. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 61(14). doi:10.1002/anie.202117324
Carboxyl Methyltransferase Catalysed Formation of Mono‐ and Dimethyl Esters under Aqueous Conditions: Application in Cascade Biocatalysis
Ward, L. C., McCue, H. V., Rigden, D. J., Kershaw, N. M., Ashbrook, C., Hatton, H., . . . Carnell, A. J. (2022). Carboxyl Methyltransferase Catalysed Formation of Mono‐ and Dimethyl Esters under Aqueous Conditions: Application in Cascade Biocatalysis. Angewandte Chemie, 134(14). doi:10.1002/ange.202117324
2021
Carboxyl Methyltransferases: Natural Functions and Potential Applications in Industrial Biotechnology
Ward, L. C., McCue, H. V., & Carnell, A. J. (2021). Carboxyl Methyltransferases: Natural Functions and Potential Applications in Industrial Biotechnology. CHEMCATCHEM, 13(1), 121-128. doi:10.1002/cctc.202001316
2019
PET hydrolysing enzymes catalyse bioplastics precursor synthesis under aqueous conditions
Parisi, D., Riley, C., Srivastava, A. S., McCue, H. V., Johnson, J. R., & Carnell, A. J. (2019). PET hydrolysing enzymes catalyse bioplastics precursor synthesis under aqueous conditions. GREEN CHEMISTRY, 21(14), 3827-3833. doi:10.1039/c9gc01284b
2017
Targeting SxIP-EB1 interaction: An integrated approach to the discovery of small molecule modulators of dynamic binding sites
Almeida, T. B., Carnell, A. J., Barsukov, I. L., & Berry, N. G. (2017). Targeting SxIP-EB1 interaction: An integrated approach to the discovery of small molecule modulators of dynamic binding sites. SCIENTIFIC REPORTS, 7. doi:10.1038/s41598-017-15502-6
The continuous oxidation of HMF to FDCA and the immobilisation and stabilisation of periplasmic aldehyde oxidase (PaoABC)
McKenna, S. M., Mines, P., Law, P., Kovacs-Schreiner, K., Birmingham, W. R., Turner, N. J., . . . Carnell, A. J. (2017). The continuous oxidation of HMF to FDCA and the immobilisation and stabilisation of periplasmic aldehyde oxidase (PaoABC). GREEN CHEMISTRY, 19, 4660-4665. doi:10.1039/c7gc01696d
Real‐Time Monitoring of Enzyme‐Catalysed Reactions using Deep UV Resonance Raman Spectroscopy
Westley, C., Fisk, H., Xu, Y., Hollywood, K. A., Carnell, A. J., Micklefield, J., . . . Goodacre, R. (2017). Real‐Time Monitoring of Enzyme‐Catalysed Reactions using Deep UV Resonance Raman Spectroscopy. Chemistry: A European Journal, 23(29), 6983-6987. doi:10.1002/chem.201701388
Absolute Quantification of Uric Acid in Human Urine Using Surface Enhanced Raman Scattering with the Standard Addition Method
Westley, C., Xu, Y., Thilaganathan, B., Carnell, A. J., Turner, N. J., & Goodacre, R. (2017). Absolute Quantification of Uric Acid in Human Urine Using Surface Enhanced Raman Scattering with the Standard Addition Method. Analytical Chemistry, 89(4), 2472-2477. doi:10.1021/acs.analchem.6b04588
2016
Label-Free Surface Enhanced Raman Scattering Approach for High-Throughput Screening of Biocatalysts
Westley, C., Xu, Y., Carnell, A. J., Turner, N. J., & Goodacre, R. (2016). Label-Free Surface Enhanced Raman Scattering Approach for High-Throughput Screening of Biocatalysts. Analytical Chemistry, 88(11), 5898-5903. doi:10.1021/acs.analchem.6b00813
2015
Galactose Oxidase Variants for the Oxidation of Amino Alcohols in Enzyme Cascade Synthesis
Herter, S., McKenna, S., Frazer, A. R., Leimkühler, S., Carnell, A., & Turner, N. J. (2015). Galactose Oxidase Variants for the Oxidation of Amino Alcohols in Enzyme Cascade Synthesis. ChemCatChem, 7(15), 2313-2317. doi:10.1002/cctc.201500218
Enzyme cascade reactions: synthesis of furandicarboxylic acid (FDCA) and carboxylic acids using oxidases in tandem
McKenna, S., Leimkühler, S., Herter, S., Turner, N. J., & Carnell, A. (2015). Enzyme cascade reactions: synthesis of furandicarboxylic acid (FDCA) and carboxylic acids using oxidases in tandem. Green Chemistry, 17(6), 3271-3275. doi:10.1039/c5gc00707k
2014
Catalytic bio–chemo and bio–bio tandem oxidation reactions for amide and carboxylic acid synthesis
Herter, S., Bechi, B., McKenna, S., Riley, C., Leimkühler, S., Turner, N. J., & Carnell, A. (2014). Catalytic bio–chemo and bio–bio tandem oxidation reactions for amide and carboxylic acid synthesis. Green Chemistry, 16(10), 4524-4529. doi:10.1039/C4GC01321B
Glycosylated yellow laccases of the basidiomycete Stropharia aeruginosa
Daroch, M., Houghton, C. A., Moore, J. K., Wilkinson, M. C., Carnell, A. J., Bates, A. D., & Iwanejko, L. A. (2014). Glycosylated yellow laccases of the basidiomycete Stropharia aeruginosa. Enzyme and Microbial Techenology, 58-59, 1-7. doi:10.1016/j.enzmictec.2014.02.003
Trifluoroibuprofen Inhibits α-Methylacyl Coenzyme A Racemase (AMACR/P504S), Reduces Cancer Cell Proliferation and Inhibits <i>in vivo</i> Tumor Growth in Aggressive Prostate Cancer Models
Festuccia, C., Gravina, G. L., Mancini, A., Muzi, P., Di Cesare, E., Kirk, R., . . . Carnell, A. J. (2014). Trifluoroibuprofen Inhibits α-Methylacyl Coenzyme A Racemase (AMACR/P504S), Reduces Cancer Cell Proliferation and Inhibits <i>in vivo</i> Tumor Growth in Aggressive Prostate Cancer Models. ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 14(7), 1031-1041. doi:10.2174/1871520614666140327152607
LIPID METHABOLISM AS THERAPEUTIC TARGET FOR PROSTATE CANCER
Festuccia, C., Mancini, A., Marampon, F., Scarsella, L., Jitariuc, A., Colapietro, A., . . . Gravina, G. L. (2014). LIPID METHABOLISM AS THERAPEUTIC TARGET FOR PROSTATE CANCER. ANTICANCER RESEARCH, 34(5), 2656-2657. Retrieved from https://www.webofscience.com/
Synthetic Cascades by Combining Evolved Biocatalysts and Artificial Enzymes
Carnell, A. J. (2014). Synthetic Cascades by Combining Evolved Biocatalysts and Artificial Enzymes. CHEMCATCHEM, 6(4), 958-960. doi:10.1002/cctc.201402143
2013
Inhibition of Human α-Methylacyl CoA Racemase (AMACR): a Target for Prostate Cancer
Carnell, A. J., Kirk, R., Smith, M., McKenna, S., Lian, L. -Y., & Gibson, R. (2013). Inhibition of Human α-Methylacyl CoA Racemase (AMACR): a Target for Prostate Cancer. CHEMMEDCHEM, 8(10), 1643-1647. doi:10.1002/cmdc.201300179
2012
Enantioselective Rhodium-Catalyzed Addition of Potassium Alkenyltrifluoroborates to Cyclic Imines
Luo, Y., Carnell, A. J., & Lam, H. W. (2012). Enantioselective Rhodium-Catalyzed Addition of Potassium Alkenyltrifluoroborates to Cyclic Imines. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 51(27), 6762-6766. doi:10.1002/anie.201202136
Enantioselective Rhodium‐Catalyzed Addition of Potassium Alkenyltrifluoroborates to Cyclic Imines
Luo, Y., Carnell, A. J., & Lam, H. W. (2012). Enantioselective Rhodium‐Catalyzed Addition of Potassium Alkenyltrifluoroborates to Cyclic Imines. Angewandte Chemie, 124(27), 6866-6870. doi:10.1002/ange.201202136
Chiral bicyclic [2.2.2] octadiene ligands for Rh-catalysed catalytic asymmetric conjugate additions to acyclic enones: a quantitative structure-property relationship
Luo, Y., Berry, N. G., & Carnell, A. J. (2012). Chiral bicyclic [2.2.2] octadiene ligands for Rh-catalysed catalytic asymmetric conjugate additions to acyclic enones: a quantitative structure-property relationship. CHEMICAL COMMUNICATIONS, 48(27), 3279-3281. doi:10.1039/c2cc17120a
2010
Chemoenzymatic Synthesis and Application of Bicyclo[2.2.2]octadiene Ligands: Increased Efficiency in Rhodium-Catalyzed Asymmetric Conjugate Additions by Electronic Tuning
Luo, Y., & Carnell, A. J. (2010). Chemoenzymatic Synthesis and Application of Bicyclo[2.2.2]octadiene Ligands: Increased Efficiency in Rhodium-Catalyzed Asymmetric Conjugate Additions by Electronic Tuning. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 49(15), 2750-2754. doi:10.1002/anie.200907033
A Practical Chemo-enzymatic Synthesis of Homochiral Bicyclo[2.2.2]octane-2,5-dione
Luo, Y., & Carnell, A. J. (2010). A Practical Chemo-enzymatic Synthesis of Homochiral Bicyclo[2.2.2]octane-2,5-dione. JOURNAL OF ORGANIC CHEMISTRY, 75(6), 2057-2060. doi:10.1021/jo9023705
A new chemoenzymatic approach to chiral bicyclic [2.2.2]octan-2,5-diones and diene ligands
Carnell, A. J. (2010). A new chemoenzymatic approach to chiral bicyclic [2.2.2]octan-2,5-diones and diene ligands. In Biocatalysis: Challenges for Pharmaceuticals & Fine Chemicals (pp. 000). London: SCI.
Characterisation and inhibition of alpha-methylacylCoA racemase (AMACR1A): a potential therapeutic target for prostate cancer
Carnell, A. J. (2010). Characterisation and inhibition of alpha-methylacylCoA racemase (AMACR1A): a potential therapeutic target for prostate cancer. In Cancer Research Scientific Symposium 2010 (pp. na). Liverpool: na.
2009
Kinetic Resolutions Using Biotransformations
Gadler, P., Faber, K., Savile, C. K., Kazlauskas, R. J., Carnell, A. J., & Breen, G. (2009). Kinetic Resolutions Using Biotransformations. In Unknown Book (pp. 117-131). Wiley. doi:10.1002/9780470748589.ch3
Increasing efficiency in the synthesis of pharmaceuticals and chiral ligands using enzymes
Carnell, A. J. (2009). Increasing efficiency in the synthesis of pharmaceuticals and chiral ligands using enzymes. In RSC Advancing the Chemical Sciences (pp. 01). London: RSC.
Microbial transformation of hydroxy metabolites of 1-oxohexyl derivatives of theobromine by <i>Cunninghamella echinulata</i> NRRL 1384
Pekala, E., Kochan, M., & Carnell, A. J. (2009). Microbial transformation of hydroxy metabolites of 1-oxohexyl derivatives of theobromine by <i>Cunninghamella echinulata</i> NRRL 1384. LETTERS IN APPLIED MICROBIOLOGY, 48(1), 19-24. doi:10.1111/j.1472-765X.2008.02478.x
2008
Designing inhibitors for alpha-methylacayl CoA racemase (AMACR), a biomarker and novel therapeutic target for prostate cancer
Carnell, A. J. (2008). Designing inhibitors for alpha-methylacayl CoA racemase (AMACR), a biomarker and novel therapeutic target for prostate cancer. In RSC Bio-Organic Group Forum (pp. 01). Leicester: RSC.
2007
Design, synthesis, and in vitro testing of α-methylacyl-CoA racemase inhibitors
Carnell, A. J., Hale, I., Denis, S., Wanders, R. J. A., Isaacs, W. B., Wilson, B. A., & Ferdinandusse, S. (2007). Design, synthesis, and in vitro testing of α-methylacyl-CoA racemase inhibitors. JOURNAL OF MEDICINAL CHEMISTRY, 50(11), 2700-2707. doi:10.1021/jm0702377
2004
Efficient large scale stereoinversion of (<i>R</i>)-ethyl 3-hydroxybutyrate
Carnell, A. J., Head, R., Bassett, D., & Schneider, M. (2004). Efficient large scale stereoinversion of (<i>R</i>)-ethyl 3-hydroxybutyrate. TETRAHEDRON-ASYMMETRY, 15(5), 821-825. doi:10.1016/j.tetasy.2003.12.005
Microbial deracemisation of <i>N</i>-(1-hydroxy-1-phenylethyl)benzamide
Cardus, G. J., Carnell, A. J., Trauthwein, H., & Riermeir, T. (2004). Microbial deracemisation of <i>N</i>-(1-hydroxy-1-phenylethyl)benzamide. TETRAHEDRON-ASYMMETRY, 15(2), 239-243. doi:10.1016/j.tetasy.2003.11.010
2003
The synthesis of buprenorphine intermediates by regioselective microbial <i>N</i>- and <i>O</i>-demethylation reactions using <i>Cunninghamella echinulata</i> NRRL 1384
Abel, A. M., Carnell, A. J., Davis, J. A., & Paylor, M. (2003). The synthesis of buprenorphine intermediates by regioselective microbial <i>N</i>- and <i>O</i>-demethylation reactions using <i>Cunninghamella echinulata</i> NRRL 1384. ENZYME AND MICROBIAL TECHNOLOGY, 33(5), 743-748. doi:10.1016/S0141-0229(03)00207-2
The synthesis of potential buprenorphine intermediates by regioselective microbial N- and O-demethylation reactions using Cunnighamella echinulata NRRL 1384
Abel, A. M., Carnell, A. J., Davis, J. A., & Paylor, M. (2003). The synthesis of potential buprenorphine intermediates by regioselective microbial N- and O-demethylation reactions using Cunnighamella echinulata NRRL 1384. Enzyme and Microbial Technology, 33, 742-747.
2002
A Novel Regiospecific N to O‐Methyl Transferase Activity in the Biotransformation of a Thebaine Derivative with Cunninghamella echinulata NRRL 1384.
Abel, A. M., Allan, G. R., Carnell, A. J., & Davis, J. A. (2002). A Novel Regiospecific N to O‐Methyl Transferase Activity in the Biotransformation of a Thebaine Derivative with Cunninghamella echinulata NRRL 1384.. ChemInform, 33(50), 186. doi:10.1002/chin.200250186
Desymmetrisation of prochiral ketones using lipases
Carnell, A. J. (2002). Desymmetrisation of prochiral ketones using lipases. JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, 19, 83-92. doi:10.1016/S1381-1177(02)00154-6
A novel regiospecific <i>N</i> to <i>O</i>-methyl transferase activity in the biotransformation of a thebaine derivative with <i>Cunninghamella echinulata</i> NRRL 1384
Abel, A. M., Allan, G. R., Carnell, A. J., & Davis, J. A. (2002). A novel regiospecific <i>N</i> to <i>O</i>-methyl transferase activity in the biotransformation of a thebaine derivative with <i>Cunninghamella echinulata</i> NRRL 1384. CHEMICAL COMMUNICATIONS, (16), 1762-1763. doi:10.1039/b204697k
Synthesis of potential buprenorphine intermediates by selective microbial <i>N</i>- and <i>O</i>-demethylation
Abel, A. M., Carnell, A. J., Davis, J. A., & Paylor, M. (2002). Synthesis of potential buprenorphine intermediates by selective microbial <i>N</i>- and <i>O</i>-demethylation. BIOTECHNOLOGY LETTERS, 24(15), 1291-1294. doi:10.1023/A:1016218211300
2001
Microbial deracemization of 1-aryl and 1-heteroaryl secondary alcohols
Allan, G. R., & Carnell, A. J. (2001). Microbial deracemization of 1-aryl and 1-heteroaryl secondary alcohols. JOURNAL OF ORGANIC CHEMISTRY, 66(19), 6495-6497. doi:10.1021/jo015770n
Chemoenzymatic synthesis of a tachykinin NK-2 antagonist
Allan, G., Carnell, A. J., Hernandez, M. L. E., & Pettman, A. (2001). Chemoenzymatic synthesis of a tachykinin NK-2 antagonist. TETRAHEDRON, 57(38), 8193-8202. doi:10.1016/S0040-4020(01)00796-7
One-pot deracemisation of an enol acetate derived from a prochiral cyclohexanone
Allan, G. R., Carnell, A. J., & Kroutil, W. (2001). One-pot deracemisation of an enol acetate derived from a prochiral cyclohexanone. TETRAHEDRON LETTERS, 42(34), 5959-5962. doi:10.1016/S0040-4039(01)01156-X
2000
Desymmetrisation of 4,4-disubstituted cyclohexanones by enzyme-catalysed resolution of their enol acetates
Allan, G., Carnell, A. J., Hernandez, M. L. E., & Pettman, A. (2000). Desymmetrisation of 4,4-disubstituted cyclohexanones by enzyme-catalysed resolution of their enol acetates. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, (20), 3382-3388. doi:10.1039/b005466f
Chemoenzymatic synthesis of a non-peptide tachykinin NK-2 antagonist
Carnell, A. J., Hernandez, M. L. E., Pettman, A., & Bickley, J. F. (2000). Chemoenzymatic synthesis of a non-peptide tachykinin NK-2 antagonist. TETRAHEDRON LETTERS, 41(35), 6929-6933. doi:10.1016/S0040-4039(00)01149-7
2-Bromocyclohexanone perhydrat - X-ray crystal structure and conformational effects on reactivity in sulfoxidations
Carnell, A. J., Clegg, W., Johnstone, R. A. W., Parsy, C. C., & Sanderson, W. R. (2000). 2-Bromocyclohexanone perhydrat - X-ray crystal structure and conformational effects on reactivity in sulfoxidations. TETRAHEDRON, 56(35), 6571-6575. doi:10.1016/S0040-4020(00)00608-6
1999
Chiral enol acetates derived from prochiral oxabicyclic ketones using enzymes
Carnell, A. J., Swain, S. A., & Bickley, J. F. (1999). Chiral enol acetates derived from prochiral oxabicyclic ketones using enzymes. TETRAHEDRON LETTERS, 40(49), 8633-8636. doi:10.1016/S0040-4039(99)01809-2
<i>N</i>,<i>N</i>-dialkylalloxans -: a new class of catalyst for dioxirane epoxidations
Carnell, A. J., Johnstone, R. A. W., Parsey, C. C., & Sanderson, W. R. (1999). <i>N</i>,<i>N</i>-dialkylalloxans -: a new class of catalyst for dioxirane epoxidations. TETRAHEDRON LETTERS, 40(45), 8029-8032. doi:10.1016/S0040-4039(99)01610-X
Chapter 2. Synthetic methods
Carnell, A. J. (1999). Chapter 2. Synthetic methods. Annual Reports Section "B" (Organic Chemistry), 95, 39-58. doi:10.1039/a808596j
Microbial transformation of (+)-10β,14-dihydroxy-<i>allo</i>-aromadendrane and (-)-<i>allo</i>-aromadendrone
de Lima, D. P., Carnell, A. J., & Roberts, S. M. (1999). Microbial transformation of (+)-10β,14-dihydroxy-<i>allo</i>-aromadendrane and (-)-<i>allo</i>-aromadendrone. JOURNAL OF CHEMICAL RESEARCH-S, (6), 396-397. doi:10.1039/a901226e
Stereoinversions using microbial redox-reactions.
Carnell, A. J. (1999). Stereoinversions using microbial redox-reactions.. Advances in biochemical engineering/biotechnology, 63, 57-72. doi:10.1007/3-540-69791-8_3
1998
2 Synthetic methods: Part (iii) Enzyme chemistry
Carnell, A. J. (1998). 2 Synthetic methods: Part (iii) Enzyme chemistry. Annual Reports on the Progress of Chemistry - Section B, 94, 39-49.
Biocatalysis of deracemization in 1,2-diols
Page, P. C. B., Carnell, A. J., & McKenzie, M. J. (1998). Biocatalysis of deracemization in 1,2-diols. SYNLETT, (7), 774-776. Retrieved from https://www.webofscience.com/
1997
Putting microbes to work
Carnell, A., & Roberts, S. (1997). Putting microbes to work. CHEMISTRY IN BRITAIN, 33(5), 49-51. Retrieved from https://www.webofscience.com/
Desymmetrisation of prochiral ketones by catalytic enantioselective hydrolysis of their enol esters using enzymes.
Carnell, A. J., Barkley, J., & Singh, A. (1997). Desymmetrisation of prochiral ketones by catalytic enantioselective hydrolysis of their enol esters using enzymes.. TETRAHEDRON LETTERS, 38(44), 7781-7784. doi:10.1016/S0040-4039(97)01817-0
Total synthesis of (-)-reserpine using the chiron approach
Hanessian, S., Pan, J. W., Carnell, A., Bouchard, H., & Lesage, L. (1997). Total synthesis of (-)-reserpine using the chiron approach. JOURNAL OF ORGANIC CHEMISTRY, 62(3), 465-473. doi:10.1021/jo961713w
1994
PREPARATION OF OPTICALLY-ACTIVE CYCLOHEXANEDIOLS AND (+)-ALPHA-HYDROXYCYCLOHEPTANONE BY AN ENZYME-CATALYZED STEREOINVERSION/OXIDATION PROCESS
CARNELL, A. J., IACAZIO, G., ROBERTS, S. M., & WILLETTS, A. J. (1994). PREPARATION OF OPTICALLY-ACTIVE CYCLOHEXANEDIOLS AND (+)-ALPHA-HYDROXYCYCLOHEPTANONE BY AN ENZYME-CATALYZED STEREOINVERSION/OXIDATION PROCESS. TETRAHEDRON LETTERS, 35(2), 331-334. doi:10.1016/S0040-4039(00)76545-2
SYNTHESIS OF (+)-BREFELDIN-A
CARNELL, A. J., CASY, G., GORINS, G., KOMPANYSAEID, A., MCCAGUE, R., OLIVO, H. F., . . . WILLETTS, A. J. (1994). SYNTHESIS OF (+)-BREFELDIN-A. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, (23), 3431-3439. doi:10.1039/p19940003431
1992
BIOTRANSFORMATIONS BY FUNGI - REGIOSELECTIVE PLUS STEREOSELECTIVE BAEYER-VILLIGER OXIDATIONS BY DEMATIACEOUS FUNGI
CARNELL, A., & WILLETTS, A. (1992). BIOTRANSFORMATIONS BY FUNGI - REGIOSELECTIVE PLUS STEREOSELECTIVE BAEYER-VILLIGER OXIDATIONS BY DEMATIACEOUS FUNGI. BIOTECHNOLOGY LETTERS, 14(1), 17-20. doi:10.1007/BF01030907
1991
MICROBIAL OXIDATION OF 7ENDO-METHYLBICYCLO[3.2.0]HEPT-2-EN-6-ONE, 7,7-DIMETHYLBICYCLO[3.2.0]HEPT-2-EN-6-ONE AND 2EXO-BROMO-3ENDO-HYDROXY-7,7-DIMETHYLBICYCLO[3.2.0]HEPTAN-6-ONE USING ACINETOBACTER NCIMB-9871
CARNELL, A. J., ROBERTS, S. M., SIK, V., & WILLETTS, A. J. (1991). MICROBIAL OXIDATION OF 7ENDO-METHYLBICYCLO[3.2.0]HEPT-2-EN-6-ONE, 7,7-DIMETHYLBICYCLO[3.2.0]HEPT-2-EN-6-ONE AND 2EXO-BROMO-3ENDO-HYDROXY-7,7-DIMETHYLBICYCLO[3.2.0]HEPTAN-6-ONE USING ACINETOBACTER NCIMB-9871. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, (10), 2385-2389. doi:10.1039/p19910002385
1990
BIOTRANSFORMATION OF CYCLOALKENONES BY FUNGI - BAEYER-VILLIGER OXIDATION OF BICYCLOHEPTENONE BY DEMATIACEOUS FUNGI
CARNELL, A., & WILLETTS, A. (1990). BIOTRANSFORMATION OF CYCLOALKENONES BY FUNGI - BAEYER-VILLIGER OXIDATION OF BICYCLOHEPTENONE BY DEMATIACEOUS FUNGI. BIOTECHNOLOGY LETTERS, 12(12), 885-890. doi:10.1007/BF01022584
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