Zobrazeno 1 - 10
of 344
pro vyhledávání: '"Toste FD"'
Publikováno v:
Shu, XZ; Zhang, M; He, Y; Frei, H; & Toste, FD. (2018). Dual Visisble Light Photoredox and Gold-Catalyzed Arylative Ring Expansion. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/4pf5x4s3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c4dfba322515e4bcc32a5e604c6e9262
https://escholarship.org/uc/item/4pf5x4s3
https://escholarship.org/uc/item/4pf5x4s3
Autor:
Buckley, AK, Cheng, T, Oh, MH, Su, GM, Garrison, J, Utan, SW, Zhu, C, Toste, FD, Goddard, WA, Toma, FM
Publikováno v:
ACS Catalysis, vol 11, iss 15
We report the discovery of a quaternary ammonium surface additive for CO2 reduction on Ag surfaces that changes the Faradaic efficiency for CO from 25% on Ag foil to 97%, while increasing the current density for CO production by a factor of 9 from 0.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1593339b3db62544dc775ca043c54842
https://escholarship.org/uc/item/82v03622
https://escholarship.org/uc/item/82v03622
Autor:
Musacchio P, Toste Fd, Raunft P, Chia-en A. Chang, Lisa Lewald, Fengchao Yu, Mrdović D, Alexey I. Nesvizhskii, Zanon Pra, Krauskopf K, Maher Te, Stephan M. Hacker, Kathrin Lang, Zollo M, Cigler M
Targeted covalent inhibitors are powerful entities in drug discovery, but their application has so far mainly been limited to addressing cysteine residues. The development of cysteine-directed covalent inhibitors has largely profited from determining
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebaafcdb9b6f84578d18a5b21bba4926
https://doi.org/10.26434/chemrxiv.14186561.v1
https://doi.org/10.26434/chemrxiv.14186561.v1
Publikováno v:
ACS Catalysis, vol 9, iss 12
Isobutene is a specialty chemical used in the production of fuel additives, polymers, and other high-value products. While normally produced by steam cracking of petroleum naphtha, there is increasing interest in identifying routes to synthesizing is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::526f2ea993e219318c78ed8d8cb0638f
https://escholarship.org/uc/item/22w352c4
https://escholarship.org/uc/item/22w352c4
Publikováno v:
Nature Catalysis, vol 1, iss 5
Ye, R; Zhao, J; Wickemeyer, BB; Toste, FD; & Somorjai, GA. (2018). Foundations and strategies of the construction of hybrid catalysts for optimized performances. Nature Catalysis, 1(5), 318-325. doi: 10.1038/s41929-018-0052-2. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/5pb2w81t
Ye, R; Zhao, J; Wickemeyer, BB; Toste, FD; & Somorjai, GA. (2018). Foundations and strategies of the construction of hybrid catalysts for optimized performances. Nature Catalysis, 1(5), 318-325. doi: 10.1038/s41929-018-0052-2. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/5pb2w81t
© 2018 Macmillan Publishers Ltd, part of Springer Nature 2018. Catalysts are generally classified into three categories: homogeneous, heterogeneous and enzyme, each evolved as an independent field. Efforts to bridge these fields are scarce but desir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::aaa1d63b44fff2639e862b4465ee2cf0
https://escholarship.org/uc/item/5pb2w81t
https://escholarship.org/uc/item/5pb2w81t
Autor:
Levin, MD, Chen, TQ, Neubig, ME, Hong, CM, Theulier, CA, Kobylianskii, IJ, Janabi, M, O'Neil, JP, Toste, FD
Publikováno v:
Levin, MD; Chen, TQ; Neubig, ME; Hong, CM; Theulier, CA; Kobylianskii, IJ; et al.(2017). A catalytic fluoride-rebound mechanism for C(sp3)-CF3bond formation. Science, 356(6344), 1272-1275. doi: 10.1126/science.aan1411. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/6255j4pr
© The Authors, some rights reserved. The biological properties of trifluoromethyl compounds have led to their ubiquity in pharmaceuticals, yet their chemical properties have made their preparation a substantial challenge, necessitating innovative ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::1a313a9bb52c49e3ce13610d986a4e51
http://www.escholarship.org/uc/item/6255j4pr
http://www.escholarship.org/uc/item/6255j4pr
Publikováno v:
Biotechnology and bioengineering, vol 113, iss 10
Baer, ZC; Bormann, S; Sreekumar, S; Grippo, A; Toste, FD; Blanch, HW; et al.(2016). Co-production of acetone and ethanol with molar ratio control enables production of improved gasoline or jet fuel blends. Biotechnology and Bioengineering, 113(10), 2079-2087. doi: 10.1002/bit.25978. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/82x4v88c
Baer, ZC; Bormann, S; Sreekumar, S; Grippo, A; Toste, FD; Blanch, HW; et al.(2016). Co-production of acetone and ethanol with molar ratio control enables production of improved gasoline or jet fuel blends. Biotechnology and Bioengineering, 113(10), 2079-2087. doi: 10.1002/bit.25978. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/82x4v88c
© 2016 Wiley Periodicals, Inc. The fermentation of simple sugars to ethanol has been the most successful biofuel process to displace fossil fuel consumption worldwide thus far. However, the physical properties of ethanol and automotive components li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::68c4a7ffdc454af1b3698c6e556cd520
https://escholarship.org/uc/item/82x4v88c
https://escholarship.org/uc/item/82x4v88c
Publikováno v:
Chemical science, vol 7, iss 4
Yang, X; & Toste, FD. (2016). Asymmetric addition of α-branched cyclic ketones to allenamides catalyzed by a chiral phosphoric acid. Chemical Science, 7(4), 2653-2656. doi: 10.1039/c5sc04202j. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/3gg2m2vd
Yang, X; & Toste, FD. (2016). Asymmetric addition of α-branched cyclic ketones to allenamides catalyzed by a chiral phosphoric acid. Chemical Science, 7(4), 2653-2656. doi: 10.1039/c5sc04202j. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/3gg2m2vd
© The Royal Society of Chemistry 2016. We describe the asymmetric addition of unactivated α-branched cyclic ketones to allenamides catalyzed by a chiral phosphoric acid, generating an all-carbon quaternary stereocenter with broad substrate scope an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5e65d9f6f15c432d5fbe0db9f102efb6
https://escholarship.org/uc/item/3gg2m2vd
https://escholarship.org/uc/item/3gg2m2vd
Publikováno v:
Journal of the American Chemical Society, vol 138, iss 2
Kawai, H; Wolf, WJ; Dipasquale, AG; Winston, MS; & Toste, FD. (2016). Phosphonium Formation by Facile Carbon-Phosphorus Reductive Elimination from Gold(III). Journal of the American Chemical Society, 138(2), 587-593. doi: 10.1021/jacs.5b10720. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/2sz2c75f
Kawai, H; Wolf, WJ; Dipasquale, AG; Winston, MS; & Toste, FD. (2016). Phosphonium Formation by Facile Carbon-Phosphorus Reductive Elimination from Gold(III). Journal of the American Chemical Society, 138(2), 587-593. doi: 10.1021/jacs.5b10720. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/2sz2c75f
© 2016 American Chemical Society. A recent trend in homogeneous gold catalysis has been the development of oxidative transformations relying on Au(I)/Au(III) redox cycling. Typically, phosphine-supported Au(I) precatalysts are used in the presence o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d22a817ff67b957b9b3bde23112f40a3
https://escholarship.org/uc/item/2sz2c75f
https://escholarship.org/uc/item/2sz2c75f
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.