Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Veronica V. Angeles"'
Autor:
Veronica V. Angeles‐Dunham, Dimitry Kurouski, Nelu Grinberg, Joshua D. Sieber, Chris H. Senanayake, Nathan K. Yee, Daniel R. Fandrick, Anita E. Mattson, Heewon Lee, Nizar Haddad, Jinhua J. Song, Divya Chennamadhavuni
Publikováno v:
Advanced Synthesis & Catalysis. 358:3062-3068
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97133ca3c432f68b02220c487ab2c64f
https://doi.org/10.1002/adsc.201600686
https://doi.org/10.1002/adsc.201600686
Publikováno v:
Organic Letters. 15:5000-5003
Nitrimines have been identified as impressive starting points for the syntheses of otherwise inaccessible, sterically encumbered enamines. The activation of nitrimines with urea catalysts for reaction with a variety of amines enables the formation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30443f8e2063f16ba9c2030e9427e375
https://doi.org/10.1021/ol402310b
https://doi.org/10.1021/ol402310b
Publikováno v:
ChemInform. 46
Nitrimines are employed as powerful reagents for metal-free formal C(sp(2) )-C(sp(2) ) cross-coupling reactions. The new chemical process is tolerant of a wide array of nitrimine and heterocyclic coupling partners giving rise to the corresponding di-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c5b74cf01a83c12b529b00719a9ea6a
https://doi.org/10.1002/chin.201520054
https://doi.org/10.1002/chin.201520054
A mild method for the deprotection of tetrahydropyranyl (THP) ethers catalyzed by iron(III) tosylate
Publikováno v:
Tetrahedron Letters. 52:6939-6941
A mild method for the deprotection of THP ethers catalyzed by iron(III) tosylate (2.0 mol %) in CH3OH has been developed. Iron(III) tosylate, Fe(OTs)3·6H2O, is a commercially available solid that is inexpensive, noncorrosive, and easy to handle. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81f765b4c818017532f11994173e38d9
https://doi.org/10.1016/j.tetlet.2011.10.068
https://doi.org/10.1016/j.tetlet.2011.10.068
Publikováno v:
Angewandte Chemie (International ed. in English). 53(52)
Nitrimines are employed as powerful reagents for metal-free formal C(sp(2) )-C(sp(2) ) cross-coupling reactions. The new chemical process is tolerant of a wide array of nitrimine and heterocyclic coupling partners giving rise to the corresponding di-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6057ab9bf140424181ebdc3d991fd0a
https://pubmed.ncbi.nlm.nih.gov/25365926
https://pubmed.ncbi.nlm.nih.gov/25365926
Publikováno v:
ChemInform. 45
N-Nitrosubstituted imines react with a wide range of secondary amines in the presence of an urea catalyst to give different sterically encumbered enamines under mild and metal-free conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d503a035826700c86b460be79e3ac97
https://doi.org/10.1002/chin.201410127
https://doi.org/10.1002/chin.201410127
Publikováno v:
Tetrahedron Letters. 51:5643-5645
A bismuth bromide-catalyzed (10.0 mol %) multicomponent reaction involving the allylation of THF- and THP-ethers, followed by in situ derivatization with acetic anhydride to generate highly functionalized esters has been developed under solvent-free
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::473a351c97439ec9f262a56631b113ac
https://doi.org/10.1016/j.tetlet.2010.08.079
https://doi.org/10.1016/j.tetlet.2010.08.079
Publikováno v:
Tetrahedron Letters. 51:1056-1058
The most common method for the deprotection of TBDMS ethers utilizes stoichiometric amounts of tetrabutylammonium fluoride, n-Bu4N + F (TBAF), which is highly corrosive and toxic. We have developed a mild and chemoselective method for the deprotectio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c852db1b98446f2b5ba473e1beab2ccf
https://doi.org/10.1016/j.tetlet.2009.12.076
https://doi.org/10.1016/j.tetlet.2009.12.076
Publikováno v:
ChemInform. 44
Incorporation of internal Lewis acid moieties onto urea scaffolds gives rise to novel tunable hydrogen bond donor catalysts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58ea4fc46a3481014059e870d78e84d5
https://doi.org/10.1002/chin.201336025
https://doi.org/10.1002/chin.201336025
Publikováno v:
Chemical communications (Cambridge, England). 49(39)
The strategic incorporation of internal Lewis acids onto urea scaffolds gives rise to a family of tunable hydrogen bond donor catalysts. The nature of the Lewis acid and associated ligands affects the urea polarization, acidity, and activity in react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00c4a8d855135644c1e595e006a6e607
https://pubmed.ncbi.nlm.nih.gov/23198283
https://pubmed.ncbi.nlm.nih.gov/23198283