Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Carl Jacky Saint-Louis"'
Autor:
Md Ackas Ali, Md Abdul Kaium, Sayed Nesar Uddin, Md Jaish Uddin, Oluseyi Olawuyi, Albert D. Campbell, Carl Jacky Saint-Louis, Mohammad A. Halim
Publikováno v:
ACS Omega, Vol 8, Iss 41, Pp 38243-38251 (2023)
Externí odkaz:
https://doaj.org/article/6c4a92bb4ba948c2a43b46fcddec4e0e
Autor:
Connor M. Meyers, Melody D. Kelley, Katie S. Keane, Silas C. Blackstock, David J. Warner, Carl Jacky Saint-Louis
Publikováno v:
The Journal of Organic Chemistry. 86:11341-11353
Azobenzenes appended with a redox-active arylamino group (redox auxiliary, RA) are prepared and shown to undergo fast, complete, and catalytic Z→E azo isomerization upon electron loss from the RA unit of the azobenzene. The RA-azo structures can be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a6bdfda3ae7cc00901bd0752ca59c96
https://doi.org/10.1021/acs.joc.1c00763
https://doi.org/10.1021/acs.joc.1c00763
Publikováno v:
PATAI'S Chemistry of Functional Groups
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1b04be70f07a7f587ab34d447ee4026
https://doi.org/10.1002/9780470682531.pat0982
https://doi.org/10.1002/9780470682531.pat0982
Autor:
Tia S. Jarvis, Luis A. Flores, Alexander R. Fisch, Vincent J. Catalano, Lei Zhu, Alan K. Schrock, Korry L. Barnes, Thomas F. Hunt, Carl Jacky Saint-Louis, Michael T. Huggins, Dolan Dean, Lyndsay Munro, Tyler J. Simmons
Publikováno v:
Tetrahedron. 74:1698-1704
Pyrrole β-amides are useful building blocks for the preparation of novel molecular architectures that can be used in supramolecular chemistry and sensor development. Under basic conditions, pyrrole β-amides with an α-aldehyde produce different con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6afdb3fc0a2e731b738af7b11f0485df
https://doi.org/10.1016/j.tet.2018.02.037
https://doi.org/10.1016/j.tet.2018.02.037
Autor:
Cathlene del Rosario, Carl Jacky Saint-Louis, William D. Coggio, Alan K. Schrock, Kenneth Ulrich, Baylen D. Thompson, Heather S. C. Hamilton
Publikováno v:
Polymer. 114:103-112
A library of 20 bio-based succinate (SA) diol, co-diol, and co-diacid polyester polyols (PESPs) was generated and characterized, giving detailed understanding for tuning of their thermal transitions and rheological parameters. SA and 1,3-propanediol,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::377fd2ba661cd6d6596af098d7207357
https://doi.org/10.1016/j.polymer.2017.02.092
https://doi.org/10.1016/j.polymer.2017.02.092
Autor:
Breanna M. Brown, Carl Jacky Saint-Louis, Michael T. Huggins, Charles Edwin Webster, Julie A. Wilson, Caleb D. C. McClinton, Alan K. Schrock, Lacey L. Magill, Robert W. Lamb, Renee Shavnore
Publikováno v:
Organicbiomolecular chemistry. 15(48)
Nine new polycyclic aromatic BN-1,2-azaborine analogues containing the N-BOH moiety were synthesized using a convenient two-step, one-pot procedure. Characterization of the prepared compounds show the luminescence wavelength and the quantum yields of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5025e6b1337fdd08d1f63e04ae6515f9
https://pubmed.ncbi.nlm.nih.gov/29170787
https://pubmed.ncbi.nlm.nih.gov/29170787
Autor:
Vincent J. Catalano, Saraphina Kim, Sarah E. Harrell, Alexander R. Fisch, Jamie A. Trindell, Andrew R. Schroeder, Pamela P. Vaughan, Julie A. Wilson, Karen S. Molek, Lacey L. Magill, Lyndsay Munro, Carl Jacky Saint-Louis, Michael T. Huggins, Alan K. Schrock, Charles Edwin Webster, Nicolle S. Jackson
Publikováno v:
The Journal of organic chemistry. 81(22)
Six new heteroaromatic polycyclic azaborine chromophores were designed, synthesized, and investigated as easily tunable high-luminescent organic materials. The impact of the nitrogen-boron-hydroxy (N-BOH) unit in the azaborines was investigated by co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c9a77ffd67091b3a6c3b0881d038781
https://pubmed.ncbi.nlm.nih.gov/27704820
https://pubmed.ncbi.nlm.nih.gov/27704820