Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Susan L. Zultanski"'
Publikováno v:
ACS Medicinal Chemistry Letters. 14:557-565
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18b00d44fd37e1118f7a71752a53a29d
https://doi.org/10.1021/acsmedchemlett.3c00037
https://doi.org/10.1021/acsmedchemlett.3c00037
Autor:
J. Cameron Twitty, Yun Hong, Bria Garcia, Stephanie Tsang, Jennie Liao, Danielle M. Schultz, Jennifer Hanisak, Susan L. Zultanski, Amelie Dion, Dipannita Kalyani, Mary P. Watson
Publikováno v:
Journal of the American Chemical Society. 145:5684-5695
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ccec728aba6a094e071676eae9030c5
https://doi.org/10.1021/jacs.2c11451
https://doi.org/10.1021/jacs.2c11451
Autor:
Peter E. Maligres, Feng Peng, Ralph Calabria, Louis-Charles Campeau, Wenyong Chen, Peter G. Dormer, Meredith Green, Cyndi Qixin He, Alan M. Hyde, Artis Klapars, Mona Utne Larsen, John Limanto, Guiquan Liu, Yizhou Liu, Aaron Moment, Timothy Nowak, Rebecca T. Ruck, Michael Shevlin, Zhiguo Jake Song, Lushi Tan, Weidong Tong, Jacob H. Waldman, Honglin Ye, Ralph Zhao, George Zhou, Michael A. Zompa, Susan L. Zultanski
Publikováno v:
Organic Process Research & Development. 26:2728-2738
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cc17f9a7ea6c08a6dbdfe3c97ba693e
https://doi.org/10.1021/acs.oprd.2c00191
https://doi.org/10.1021/acs.oprd.2c00191
Autor:
Ryan D. Cohen, Nadine Kuhl, Artis Klapars, Lauren Weisel, Susan L. Zultanski, Jamie M. McCabe Dunn, Jon A. Jurica, Anil R. Ekkati, Donald R. Gauthier, Mikhail Reibarkh, Wendy Zhong, Jungchul Kim
Publikováno v:
Organic Process Research & Development. 25:597-607
Cyclodextrin (CD) perfunctionalization reactions are challenging to study because they proceed through a number of regioisomeric intermediates, thus warranting creative approaches to understanding ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b22a9cef45b0ed5c11d91b36edd5d892
https://doi.org/10.1021/acs.oprd.0c00249
https://doi.org/10.1021/acs.oprd.0c00249
Autor:
Susan L. Zultanski, Cameron C Germe, Mycah R Uehling, Nilay Hazari, Emily L Barth, David J. Charboneau, Brandon Q. Mercado, Haotian Huang
Publikováno v:
J Am Chem Soc
The syntheses of four new tunable homogeneous organic reductants based on a tetraaminoethylene scaffold are reported. The new reductants have enhanced air-stability compared to current homogeneous reductants for metal mediated reductive transformatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcc7a74939b59d1b10f802d9de39e7aa
https://europepmc.org/articles/PMC8678384/
https://europepmc.org/articles/PMC8678384/
Autor:
Kevin R. Campos, Lushi Tan, Daniel A. DiRocco, Tyler A. Davis, Rebecca T. Ruck, Peter E. Maligres, Artis Klapars, John Y. L. Chung, Zhiguo Jake Song, Mona Utne Larsen, Wenyong Chen, Timothy J. Wright, Amude M. Kassim, Guiquan Liu, John Limanto, Aaron Moment, Stephen M. Dalby, Susan L. Zultanski, Louis-Charles Campeau, Ralph Calabria, Michael Shevlin, Feng Peng, Bryon Simmons, Alan M. Hyde
Publikováno v:
Chemical Science
An efficient route to the HCV antiviral agent uprifosbuvir was developed in 5 steps from readily available uridine in 50% overall yield. This concise synthesis was achieved by development of several synthetic methods: (1) complexation-driven selectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::619837ac9c9305f72e68520fc73a7a54
https://pubmed.ncbi.nlm.nih.gov/34276931
https://pubmed.ncbi.nlm.nih.gov/34276931
Publikováno v:
ACS Catal
A dual catalytic system for cross-electrophile coupling reactions between aryl halides and alkyl halides that features a Ni catalyst, a Co cocatalyst, and a mild homogeneous reductant is described. Mechanistic studies indicate that the Ni catalyst ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa62b632e2ebf898fad7f08cf0f45480
https://pubmed.ncbi.nlm.nih.gov/33628617
https://pubmed.ncbi.nlm.nih.gov/33628617
A new dual catalytic system for cross-electrophile coupling reactions between aryl and alkyl halides that features a Ni catalyst, a Co co-catalyst, and a mild homogeneous reductant, is described. This is a unique combination of reagents for cross-ele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0c1c8909b7a6023ab40163813485817
https://doi.org/10.26434/chemrxiv.12574664
https://doi.org/10.26434/chemrxiv.12574664
Autor:
Michael Shevlin, Yong-Li Zhong, Alan M. Hyde, Jacob H. Waldman, Feng Peng, Susan L. Zultanski
Publikováno v:
Organic Process Research & Development. 21:1355-1370
Overarching principles for salting-out extraction are long-established but poorly disseminated. We highlight the opportunity for more widespread application of this technique using the Hofmeister series as a foundational basis for choosing the right
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94fa0fe2a64b56e46b71a656dfd1460a
https://doi.org/10.1021/acs.oprd.7b00197
https://doi.org/10.1021/acs.oprd.7b00197
Publikováno v:
Journal of the American Chemical Society. 138:6416-6419
A modular Cu/ABNO catalyst system has been identified that enables efficient aerobic oxidative coupling of alcohols and amines to amides. All four permutations of benzylic/aliphatic alcohols and primary/secondary amines are viable in this reaction, e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d83fbe5c92b42952c1f66d35528df063
https://doi.org/10.1021/jacs.6b03931
https://doi.org/10.1021/jacs.6b03931