Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Casey M. Murphy"'
Autor:
Conrad Richtscheidt, Erin Terranova, James L. Burke, JoAnn K. Girel, Mark Krzeszowiec, Zachary Gaskell, Justin J. Maresh, Arthur A. Ralko, Casey M. Murphy, Thomas E. Speltz
Publikováno v:
Synlett. 25:2891-2894
A detailed account regarding the synthesis of 2- and 5-halogenated dopamine is given. The key step is a chemoselective reduction of a nitrostyrene by Zn/HCl at 0 °C. These conditions represent a simple, low-cost alternative to reduction by water-sen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e88304692e4c85e364f0bac6359df29f
https://doi.org/10.1055/s-0034-1379481
https://doi.org/10.1055/s-0034-1379481
Autor:
Sean O. Crowe, Justin J. Maresh, Casey M. Murphy, Mark Krzeszowiec, Michael W. Mullowney, Mark D. Aparece, Arthur A. Ralko
Publikováno v:
Tetrahedron Letters. 55:5047-5051
A convenient method for oxidative decarboxylation of α-amino acids is presented. The aldehyde products may be isolated or converted to tetrahydroisoquinolines by addition of dopamine via Pictet–Spengler reaction. Racemic products are generated by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d166cfe4a1004aa26ad705452f64b3bf
https://doi.org/10.1016/j.tetlet.2014.07.043
https://doi.org/10.1016/j.tetlet.2014.07.043
Autor:
Gregory B. Kharas, Sonia E. Chavez, Harrison S. Browning, Jennifer A. Sepe, Mario E. Romanelli, Melissa K. Susnis, Gonzalo Choque-Gonzales, Kevin N. Fuentes, Ralitza A. Treneva, Casey M. Murphy
Publikováno v:
Journal of Macromolecular Science, Part A. 51:751-755
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5e5c6af174ed84850fdbf3caa31fe1d
https://doi.org/10.1080/10601325.2014.937119
https://doi.org/10.1080/10601325.2014.937119
Autor:
Sean O. Crowe, Mark D. Aparece, Michael W. Mullowney, Arthur A. Ralko, Justin J. Maresh, Casey M. Murphy, Mark Krzeszowiec
Publikováno v:
ChemInform. 46
Oxidative decarboxylation of α-amino acids provides the corresponding aldehydes which are converted into tetrahydroquinolines by addition of dopamine via Pictet—Spengler reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a84421e43d64b7168394db48f0d351f
https://doi.org/10.1002/chin.201507219
https://doi.org/10.1002/chin.201507219