Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vijayalakshmi A. Moorthie"'
Publikováno v:
ARKIVOC, Vol 2007, Iss 5, Pp 139-151 (2006)
Externí odkaz:
https://doaj.org/article/a67c5048f96d411ab9593ffbd9ec4b43
Autor:
John C. Vederas, Jin W. Choi, Suzanne M. Ma, Vijayalakshmi A. Moorthie, K. K. Michael Lee, James T. Kealey, Jesse W.-H. Li, Hui Zhou, Xinkai Xie, Yi Tang, Nancy A. Da Silva
Publikováno v:
Science. 326:589-592
Dissecting Megaenzyme Mechanisms Filamentous fungi contain a class of multidomain enzymes, the highly-reducing iterative polyketide synthases (HR-IPKSs), which produce important natural products such as the cholesterol-lowering drug lovastatin. To pr
Autor:
Christopher M. Diaper, Bindu Pillai, Vijayalakshmi A. Moorthie, Michael N.G. James, Marco J. van Belkum, Sandra L. Marcus, Maia M. Cherney, John C. Vederas
Publikováno v:
Journal of molecular biology. 385(2)
Diaminopimelate (DAP) epimerase is a key enzyme for the biosynthesis of lysine in plants. Lysine is an essential dietary nutrient for mammals. In both plants and bacteria, DAP epimerase catalyzes the interconversion of LL-DAP and DL(meso)-DAP. The ab
Autor:
Vijayalakshmi A. Moorthie, Mark R. Crimmin, Marco Ferrara, Johnathan V. Matlock, Mehrnoosh Ostovar, Lorenz E. Löffler, Mushtaq Ahmad, Varinder K. Aggarwal, Yunus E. Türkmen, Michael Alan Shaw, C. Chun Chen, Oleksandr Zhurakovskyi
Publikováno v:
Zhurakovskyi, O, Türkmen, Y E, Löffler, L E, Moorthie, V A, Chen, C C, Shaw, M A, Crimmin, M R, Ferrara, M, Ahmad, M, Ostovar, M, Matlock, J V & Aggarwal, V K 2018, ' Enantioselective Synthesis of the Cyclopiazonic Acid Family Using Sulfur Ylides ', Angewandte Chemie-International Edition, vol. 57, no. 5, pp. 1346–1350 . https://doi.org/10.1002/anie.201712065
Angewandte Chemie (International Ed. in English)
Angewandte Chemie International Edition
Angewandte Chemie (International Ed. in English)
Angewandte Chemie International Edition
A convergent, nine‐step (LLS), enantioselective synthesis of α‐cyclopiazonic acid and related natural products is reported. The route features a) an enantioselective aziridination of an imine with a chiral sulfur ylide; b) a bioinspired (3+2)‐
Publikováno v:
University of Bristol-PURE
ARKIVOC, Vol 2007, Iss 5, Pp 139-151 (2006)
ARKIVOC, Vol 2007, Iss 5, Pp 139-151 (2006)
An efficient, high yielding synthesis of ethyl 5-hydroxymethyl-3-methylisoxazole-4-carboxylate has been developed, based on a procedure by Gelin which involves reaction of ethyl acetoacetate with chloroacetyl chloride followed by treatment with hydro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70737cbbecfcc877e8d663b41dffab9d
https://research-information.bris.ac.uk/en/publications/e5fa03ec-8b20-4708-b611-83f0a2d18149
https://research-information.bris.ac.uk/en/publications/e5fa03ec-8b20-4708-b611-83f0a2d18149