Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Selvam Raju"'
Autor:
Bhupendra Adhikari, Selvam Raju, Raymond Femi Awoyemi, Bruno Donnadieu, David O. Wipf, Sean L. Stokes, Joseph P. Emerson
Publikováno v:
Molecules, Vol 29, Iss 15, p 3542 (2024)
Three new tridentate copper(II) N-heterocyclic carbene (NHC) complexes have been obtained and characterized with symmetrical C-4 substitutions on their pendent pyridine rings. Substitutions including methyl (Me), methoxy (OMe), and chloro (Cl) groups
Externí odkaz:
https://doaj.org/article/9ad61c331080470bac5a242daa31a902
Autor:
Mohsen Teimouri, Selvam Raju, Edward Acheampong, Allison N. Schmittou, Bruno Donnadieu, David O. Wipf, Brad S. Pierce, Sean L. Stokes, Joseph P. Emerson
Publikováno v:
Molecules, Vol 29, Iss 3, p 730 (2024)
A new tridentate Cu2+ complex based on (E)-1-(pyridin-2-yl)-N-(quinolin-8-yl)methanimine (PQM) was generated and characterized to support the activation of diazo compounds for the formation of new C–N bonds. This neutral Schiff base ligand was stru
Externí odkaz:
https://doaj.org/article/d9e6526088c54f4d969687e1dc90b7f3
Autor:
SELVAM RAJU
107
Development of three new methods for o-arylaniline and benzofulvene functionalization through palladium catalysis are presented. Transition-metal-catalyzed C−C, C-N, and C-X bond formation reaction by uniting readily available π-component
Development of three new methods for o-arylaniline and benzofulvene functionalization through palladium catalysis are presented. Transition-metal-catalyzed C−C, C-N, and C-X bond formation reaction by uniting readily available π-component
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/fu2m56
Publikováno v:
Organic Letters. 23:6212-6216
The reaction of o-benzofulvene with TfOH leads to intramolecular cyclization through novel C-C and C-N bond formation, resulting in the formation of 5H,10'H-spiro[benzo[k]phenanthridine-5,6'-dibenzopentalene]. This protocol provides a new molecular f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46d9f049d0192d9f744d731e9f882751
https://doi.org/10.1021/acs.orglett.1c01809
https://doi.org/10.1021/acs.orglett.1c01809
Autor:
Selvam Raju, Patrick E. Sheridan, Alanna K. Hauer, Allyn E. Garrett, Danielle E. McConnell, Justin A. Thornton, Sean L. Stokes, Joseph P. Emerson
Publikováno v:
Chemistry & Biodiversity. 19
The coupling of phenylboronic acids with poorly-activated imidazoles is studied as a model system to explore the use of copper-catalyzed Chan-Evans-Lam (CEL) coupling for targeted C-N bond forming reactions. Optimized CEL reaction conditions are repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9af56dbfa6882bab986e9176d43db56f
https://doi.org/10.1002/cbdv.202200327
https://doi.org/10.1002/cbdv.202200327
Autor:
S. Erfan Masaeli, Mohsen Teimouri, Bhupendra Adhikari, Mahshid Attarroshan, James W. Akin, Selvam Raju, Sean L. Stokes, Joseph P. Emerson
Publikováno v:
Tetrahedron Letters. 122:154520
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14b4861f59a77d4913e4d53974a3f318
https://doi.org/10.1016/j.tetlet.2023.154520
https://doi.org/10.1016/j.tetlet.2023.154520
Publikováno v:
Organic Letters. 22:6252-6256
A novel and efficient reductive N-alkenylation of iminoquinones with electron-deficient olefins has been successfully developed by Pd(II)-catalyzed redox-neutral reactions, which provides a synthes...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfe4bd674379c1e1b8e666bcb2a3b9d4
https://doi.org/10.1021/acs.orglett.0c01929
https://doi.org/10.1021/acs.orglett.0c01929
Publikováno v:
Organic letters. 23(16)
The reaction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bc9dfc22b985054802026e889c70049e
https://pubmed.ncbi.nlm.nih.gov/34355911
https://pubmed.ncbi.nlm.nih.gov/34355911
Publikováno v:
Organic letters. 22(16)
A novel and efficient reductive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fb7ed2fb3718c774cef746cbcffb1ba6
https://pubmed.ncbi.nlm.nih.gov/32692563
https://pubmed.ncbi.nlm.nih.gov/32692563
Publikováno v:
Advanced Synthesis & Catalysis. 361:683-689
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::103d4f280223e6b9ebfe5facedbe2ca4
https://doi.org/10.1002/adsc.201801352
https://doi.org/10.1002/adsc.201801352