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of 7
pro vyhledávání: '"Ryan Littich"'
Autor:
Dominik Polterauer, Dominique M. Roberge, Paul Hanselmann, Ryan Littich, Christopher A. Hone, C. Oliver Kappe
Publikováno v:
Reaction Chemistry & Engineering. 7:2582-2592
We develop a continuous flow protocol for the synthesis of sulfonyl chlorides from disulfides and thiols, using 1,3-dichloro-5,5-dimethylhydantoin (DCH) as a dual-function reagent for oxidative chlorination.
Autor:
Niteen Vaidya, David Deutsch, Jennifer Maclachlan, Mukund Chorghade, Ryan Littich, Carlyn Burton, James Skinner, Adam Sussman, Abhishek Kantak, Janet Bryant, Joseph Sabol, George Ruger
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1429c327d661fdc0265930afcbc76f2
https://doi.org/10.1021/scimeetings.0c06983
https://doi.org/10.1021/scimeetings.0c06983
Publikováno v:
INFORM: International News on Fats, Oils, and Related Materials. 26:558-561
Autor:
Ryan Littich, Peter J. H. Scott
Publikováno v:
Angewandte Chemie International Edition. 51:1106-1109
Positron (b) emission tomography (PET) is a powerful, noninvasive tool for the in vivo, three-dimensional imaging of physiological structures and processes. PET imaging involves the incorporation of short-lived radionuclides, particularly carbon-11 a
Publikováno v:
ChemInform. 45
Positron (β + ) emission tomography (PET) is a powerful, noninvasive tool for the in vivo, three-dimensional imaging of physiological structures and biochemical pathways. The continued growth of PET imaging relies on a corresponding increase in acce
Publikováno v:
Current topics in medicinal chemistry. 14(7)
Positron (β + ) emission tomography (PET) is a powerful, noninvasive tool for the in vivo, three-dimensional imaging of physiological structures and biochemical pathways. The continued growth of PET imaging relies on a corresponding increase in acce
Autor:
Philip Magnus, Ryan Littich
Publikováno v:
Organic letters. 11(17)
Synthesis of the BCD ring system of cortistatin A has been accomplished in 9 steps and 30% overall yield starting from commercially available 2-methylcyclopent-2-enone. Key transformations include the addition of cyclopropenyllithium 16 to aldehyde 1