Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Simon J, Charnock"'
Autor:
Henry Gould, William Cheung, James D. Finnigan, José Muñoz-Muñoz, Simon J. Charnock, Gary W. Black
Publikováno v:
Metabolites, Vol 13, Iss 9, p 1010 (2023)
Escherichia coli is an invaluable research tool for many fields of biology, in particular for the production of recombinant enzymes. However, the activity of many such recombinant enzymes cannot be determined using standard biochemical assays, as oft
Externí odkaz:
https://doaj.org/article/9100f8bd24d64e808d5ab900fc20a501
Autor:
Emily E. Kempa, James L. Galman, Fabio Parmeggiani, James R. Marshall, Julien Malassis, Clement Q. Fontenelle, Jean-Baptiste Vendeville, Bruno Linclau, Simon J. Charnock, Sabine L. Flitsch, Nicholas J. Turner, Perdita E. Barran
Publikováno v:
JACS Au, Vol 1, Iss 4, Pp 508-516 (2021)
Externí odkaz:
https://doaj.org/article/34a43ef107ba44e88b736b23d77fadc9
Autor:
Claire G. Page, Jingzhe Cao, Daniel G. Oblinsky, Samantha N. MacMillan, Shiva Dahagam, Ruth M. Lloyd, Simon J. Charnock, Gregory D. Scholes, Todd K. Hyster
Publikováno v:
Journal of the American Chemical Society. 145:11866-11874
Autor:
Vanessa Harawa, Thomas W. Thorpe, James R. Marshall, Jack J. Sangster, Amelia K. Gilio, Lucian Pirvu, Rachel S. Heath, Antonio Angelastro, James D. Finnigan, Simon J. Charnock, Jordan W. Nafie, Gideon Grogan, Roger C. Whitehead, Nicholas J. Turner
Publikováno v:
Journal of the American Chemical Society. 144:21088-21095
The development of efficient and sustainable methods for the synthesis of nitrogen heterocycles is an important goal for the chemical industry. In particular, substituted chiral piperidines are prominent targets due to their prevalence in medicinally
Autor:
Nicholas J. Weise, Syed T. Ahmed, Fabio Parmeggiani, James L. Galman, Mark S. Dunstan, Simon J. Charnock, David Leys, Nicholas J. Turner
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
Abstract The suite of biological catalysts found in Nature has the potential to contribute immensely to scientific advancements, ranging from industrial biotechnology to innovations in bioenergy and medical intervention. The endeavour to obtain a cat
Externí odkaz:
https://doaj.org/article/7bb9d4a74a89407ab9d72a5cb2e2d579
Autor:
Haigen Fu, Jingzhe Cao, Tianzhang Qiao, Yuyin Qi, Simon J. Charnock, Samuel Garfinkle, Todd K. Hyster
Publikováno v:
Nature
The catalytic asymmetric construction of Csp(3)–Csp(3) bonds remains one of the foremost challenges in organic synthesis.(1) Metal-catalyzed cross-electrophile couplings (XEC) have emerged as a powerful tool for C–C bond formation.(2–5) However
Autor:
Yuriy V. Sheludko, Sjoerd Slagman, Samantha Gittings, Simon J. Charnock, Henrik Land, Per Berglund, Wolf‐Dieter Fessner
Publikováno v:
Advanced Synthesis & Catalysis. 364:2972-2981
ATAs engineered for having an enlarged small binding pocket were applied for the synthesis of enantiomerically pure (R)-benzo[1,3]dioxol-5-yl-butylamine, a chiral component of human leukocyte elastase inhibitor DMP 777 (L-694,458). Kinetic resolution
Publikováno v:
Organic Process Research & Development. 26:2096-2101
Autor:
James R. Marshall, Han Bevinakatti, Joan Citoler, Nicholas J. Turner, James Finnigan, Vanessa Harawa, Simon J. Charnock
Publikováno v:
Angewandte Chemie International Edition
Citoler, J, Harawa, V, Marshall, J R, Bevinakatti, H, Finnigan, J D, Charnock, S J & Turner, N J 2021, ' Synthesis of Pharmaceutically Relevant 2-Aminotetralin and 3-Aminochroman Derivatives via Enzymatic Reductive Amination ', Angewandte Chemie-International Edition, vol. 60, no. 46, pp. 24456-24460 . https://doi.org/10.1002/anie.202110321
Citoler, J, Harawa, V, Marshall, J R, Bevinakatti, H, Finnigan, J D, Charnock, S J & Turner, N J 2021, ' Synthesis of Pharmaceutically Relevant 2-Aminotetralin and 3-Aminochroman Derivatives via Enzymatic Reductive Amination ', Angewandte Chemie-International Edition, vol. 60, no. 46, pp. 24456-24460 . https://doi.org/10.1002/anie.202110321
2-Aminotetralin and 3-aminochroman derivatives are key structural motifs present in a wide range of pharmaceutically important molecules. Herein, we report an effective biocatalytic approach towards these molecules through the enantioselective reduct
Autor:
Simon J. Charnock, Đurđa Vasić-Rački, Pere Clapés, Morana Česnik, Martina Sudar, Z. Findrik Blažević, Karel Hernández
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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L-Homoserine is an important compound and a building block in chemical and pharmaceutical industry. The one-pot cascade synthesis of L-homoserine with substrate recycling catalysed by an aldolase and a transaminase was investigated in detail, with sp