Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Travis J. DeLano"'
Autor:
Caitlin R. Lacker, Travis J. DeLano, Emily P. Chen, Jongrock Kong, Kevin M. Belyk, Tiffany Piou, Sarah E. Reisman
Publikováno v:
Journal of the American Chemical Society. 144:20190-20195
Autor:
Sabrina Absalon, Karin Blomqvist, Rachel M. Rudlaff, Travis J. DeLano, Michael P. Pollastri, Jeffrey D. Dvorin
Publikováno v:
mBio, Vol 9, Iss 1 (2018)
ABSTRACT The human malaria parasite Plasmodium falciparum requires efficient egress out of an infected red blood cell for pathogenesis. This egress event is highly coordinated and is mediated by several signaling proteins, including the plant-like P.
Externí odkaz:
https://doaj.org/article/9ff6ac7be22a4dbebd4235997aee08ce
Autor:
Caitlin R, Lacker, Travis J, DeLano, Emily P, Chen, Jongrock, Kong, Kevin M, Belyk, Tiffany, Piou, Sarah E, Reisman
Publikováno v:
Journal of the American Chemical Society. 144(44)
An asymmetric cross-coupling of α
Publikováno v:
Organic Synth
[Image: see text]
Autor:
Sarah E. Reisman, Sara E. Dibrell, Leah Cleary, Caitlin R. Lacker, Adam R. Pancoast, Kelsey E. Poremba, Travis J. DeLano, Matthew S. Sigman
Publikováno v:
Chemical Science
An asymmetric reductive cross-coupling of α-chloroesters and (hetero)aryl iodides is reported. This nickel-catalyzed reaction proceeds with a chiral BiOX ligand under mild conditions, affording α-arylesters in good yields and enantioselectivities.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f478b36d4b38e65ddb6c68144f66eb91
https://resolver.caltech.edu/CaltechAUTHORS:20210113-152642442
https://resolver.caltech.edu/CaltechAUTHORS:20210113-152642442
Publikováno v:
Organic Syntheses. :177-191
Autor:
Serim Ryou, Sarah E. Reisman, Michael R. Maser, Yisong Yue, Alexander Y. Cui, Travis J. DeLano
Publikováno v:
Journal of chemical information and modeling. 61(1)
Machine-learned ranking models have been developed for the prediction of substrate-specific cross-coupling reaction conditions. Data sets of published reactions were curated for Suzuki, Negishi, and C-N couplings, as well as Pauson-Khand reactions. S
Autor:
Serim Ryou, Alexander Y. Cui, Michael R. Maser, Sarah E. Reisman, Yisong Yue, Travis J. DeLano
Machine-learned ranking models have been developed for the prediction of substrate-specific cross-coupling reaction conditions. Datasets of published reactions were curated for Suzuki, Negishi, and C–N couplings, as well as Pauson–Khand reactions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c8458d53e1645f9bbecf743ca6c8ea7
https://doi.org/10.26434/chemrxiv.13087769.v1
https://doi.org/10.26434/chemrxiv.13087769.v1
Autor:
Miguel Navarro, Quillon J. Simpson, Travis J. DeLano, Maria Santos Martinez-Martinez, Raquel García-Hernández, Rosario Diaz-Gonzalez, Westley Tear, Guiomar Pérez-Moreno, William G. Devine, Lori Ferrins, Dolores González-Pacanowska, Luis M. Ruiz-Pérez, Melanie G. Fritsche, Katherine M. Schneider, Michael P. Pollastri, Francisco Gamarro, John K. Fisher, Cristina Bosch-Navarrete, Pilar Manzano-Chinchon, Vivian Hilborne, Dana M. Klug, Raeann M. Dalton, Gloria Ceballos-Pérez, Eftychia M. Mavrogiannaki, Melissa J. Buskes
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
RSC Med Chem
instname
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
RSC Med Chem
Human African trypanosomiasis is a neglected tropical disease (NTD) that is fatal if left untreated. Although approximately 13 million people live in moderate- to high-risk areas for infection, current treatments are plagued by problems with safety,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c419df9071d8f28b3bdefbdbcc538de7
http://hdl.handle.net/10261/246477
http://hdl.handle.net/10261/246477
Autor:
Sarah E. Reisman, Travis J. DeLano
Publikováno v:
ACS Catal
An electrochemically driven enantioselective nickel-catalyzed reductive cross-coupling of alkenyl bromides and benzyl chlorides is reported. The reaction forms products bearing allylic stereogenic centers with good enantioselectivity under mild condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46dfa7478cf0c1410f05780bce9f4405
https://resolver.caltech.edu/CaltechAUTHORS:20190625-112222475
https://resolver.caltech.edu/CaltechAUTHORS:20190625-112222475