Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Christopher K. Prier"'
Autor:
Christopher K. Prier, Karla Camacho Soto, Jacob H. Forstater, Nadine Kuhl, Jeffrey T. Kuethe, Wai Ling Cheung-Lee, Michael J. Di Maso, Claire M. Eberle, Shane T. Grosser, Hsing-I Ho, Erik Hoyt, Anne Maguire, Kevin M. Maloney, Amanda Makarewicz, Jonathan P. McMullen, Jeffrey C. Moore, Grant S. Murphy, Karthik Narsimhan, Weilan Pan, Nelo R. Rivera, Anumita Saha-Shah, David A. Thaisrivongs, Deeptak Verma, Adeya Wyatt, Daniel Zewge
Publikováno v:
ACS Catalysis. :7707-7714
Enzymes are capable of unique and selective transformations that can enable sustainable chemical production. While many industrial processes have been developed using free enzymes in aqueous solutions, immobilizing enzymes on a solid support can offe
Autor:
Nadine Kuhl, Ben W. H. Turnbull, Yining Ji, Reed T. Larson, Michael Shevlin, Christopher K. Prier, Cheol K. Chung, Richard Desmond, Erik Guetschow, Cyndi Qixin He, Tetsuji Itoh, Jeffrey T. Kuethe, Justin A. Newman, Mikhail Reibarkh, Nelo R. Rivera, Gao Shang, Zhixun Wang, Daniel Zewge, David A. Thaisrivongs
Publikováno v:
Green Chemistry. 25:606-613
The development of a protecting group-free, 2-step synthesis of 5-amino-2-hydroxymethyltetrahydropyran 1a from biorenewable Cyrene™ is described which renders access to BTK-inhibitor nemtabrutinib (2) more efficient and sustainable.
Autor:
Yuxuan Ye, Jingzhe Cao, Daniel G. Oblinsky, Deeptak Verma, Christopher K. Prier, Gregory D. Scholes, Todd K. Hyster
Publikováno v:
Nature Chemistry. 15:206-212
Publikováno v:
Advanced Synthesis & Catalysis. 361:5140-5143
Autor:
Christopher K. Prier
Publikováno v:
Nature Catalysis. 4:348-349
Creating enzymes with new capabilities is a key goal for synthetic biology and sustainable chemistry. Now, computational approaches have been used to quickly achieve leaps in enzyme function, providing a versatile platform for biocatalytic hydroamina
Chiral 1,2‐amino alcohols are widely represented in biologically active compounds from neurotransmitters to antivirals. While many synthetic methods have been developed for accessing amino alcohols, the direct aminohydroxylation of alkenes to unpro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4045db16d52904dd5e9c79fccedc91ec
https://resolver.caltech.edu/CaltechAUTHORS:20190102-135256908
https://resolver.caltech.edu/CaltechAUTHORS:20190102-135256908
Autor:
Christopher K. Prier, Audrey Huang, Christopher C. Farwell, Frances H. Arnold, Todd K. Hyster
Publikováno v:
Angewandte Chemie International Edition. 55:4711-4715
Sigmatropic rearrangements, while rare in biology, offer opportunities for the efficient and selective synthesis of complex chemical motifs. A “P411” serine-ligated variant of cytochrome P450_(BM3) has been engineered to initiate a sulfimidation/
Autor:
Birgit Kosjek, Christopher K. Prier
Publikováno v:
Current opinion in chemical biology. 49
Redox enzymes offer many powerful transformations for the efficient industrial-scale synthesis of diverse chemicals desired by society. Here we survey recent preparative applications of redox enzymes, highlighting both mature enzyme platforms and pro
Publikováno v:
Visible Light Photocatalysis in Organic Chemistry ISBN: 9783527674145
Visible Light Photocatalysis in Organic Chemistry
Visible Light Photocatalysis in Organic Chemistry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42b9696473f76dd944b1f371eee99b2d
https://doi.org/10.1002/9783527674145.ch10
https://doi.org/10.1002/9783527674145.ch10
Autor:
Ruijie K. Zhang, Sabine Brinkmann-Chen, Christopher K. Prier, Andrew R. Buller, Frances H. Arnold
C–H bonds are ubiquitous structural units of organic molecules. Although these bonds are generally considered to be chemically inert, the recent emergence of methods for C–H functionalization promises to transform the way synthetic chemistry is p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::862272734d50585c19207a4f1a90438b
https://resolver.caltech.edu/CaltechAUTHORS:20170413-120718900
https://resolver.caltech.edu/CaltechAUTHORS:20170413-120718900