- Home
- Search Results
- Page 1 of 1
Search for: All records
-
Total Resources3
- Resource Type
-
0000000003000000
- More
- Availability
-
30
- Author / Contributor
- Filter by Author / Creator
-
-
Dinh, Andrew N. (3)
-
Gustafson, Jeffrey L. (2)
-
Aceves, Ernesto Millan (1)
-
Albright, Samuel T. (1)
-
Cedano, Mario R. (1)
-
Do, Quynh (1)
-
Lee, David D. (1)
-
Maddox, Sean M. (1)
-
Nalbandian, Christopher J. (1)
-
Nguyen, Ashley D. (1)
-
Saputra, Mirza A. (1)
-
Seguin, Ryan P. (1)
-
Smith, Diane K. (1)
-
Vaidya, Sagar D. (1)
-
Xu, Libin (1)
-
Zhang, Rutan (1)
-
#Tyler Phillips, Kenneth E. (0)
-
#Willis, Ciara (0)
-
& Abreu-Ramos, E. D. (0)
-
& Abramson, C. I. (0)
-
- Filter by Editor
-
-
& Spizer, S. M. (0)
-
& . Spizer, S. (0)
-
& Ahn, J. (0)
-
& Bateiha, S. (0)
-
& Bosch, N. (0)
-
& Brennan K. (0)
-
& Brennan, K. (0)
-
& Chen, B. (0)
-
& Chen, Bodong (0)
-
& Drown, S. (0)
-
& Ferretti, F. (0)
-
& Higgins, A. (0)
-
& J. Peters (0)
-
& Kali, Y. (0)
-
& Ruiz-Arias, P.M. (0)
-
& S. Spitzer (0)
-
& Sahin. I. (0)
-
& Spitzer, S. (0)
-
& Spitzer, S.M. (0)
-
(submitted - in Review for IEEE ICASSP-2024) (0)
-
-
Have feedback or suggestions for a way to improve these results?
!
Note: When clicking on a Digital Object Identifier (DOI) number, you will be taken to an external site maintained by the publisher.
Some full text articles may not yet be available without a charge during the embargo (administrative interval).
What is a DOI Number?
Some links on this page may take you to non-federal websites. Their policies may differ from this site.
-
Dinh, Andrew N.; Nguyen, Ashley D.; Aceves, Ernesto Millan; Albright, Samuel T.; Cedano, Mario R.; Smith, Diane K.; Gustafson, Jeffrey L. (, Synlett)We report studies on the photocatalytic formation of C–S bonds to form benzothiazoles via an intramolecular cyclization and sulfenylated indoles via an intermolecular reaction. Cyclic voltammetry (CV) and density functional theory studies suggest that benzothiazole formation proceeds via a mechanism that involves an electrophilic sulfur radical, while the indole sulfenylation likely proceeds via a nucleophilic sulfur radical adding into a radical cationic indole. These conditions were successfully extended to several thiobenzamides and indole substrates.more » « less
-
Do, Quynh; Lee, David D.; Dinh, Andrew N.; Seguin, Ryan P.; Zhang, Rutan; Xu, Libin (, The Journal of Organic Chemistry)
An official website of the United States government
