Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tanja Kaehler"'
Publikováno v:
Dalton Transactions. 52:1820-1825
A series of fluorinated triaryl borates B(OArF)3 (ArF = 2-FC6H4, 3-FC6H4, 4-FC6H4, 2,4-F2C6H3, 3,5-F2C6H3, 2,3,4-F3C6H2, 2,4,6-F3C6H2, 3,4,5-F3C6H2) have been prepared and isolated from the reactions of the mono-, di-, or tri-fluorophenol with BCl3.
Autor:
Nusaybah Alotaibi, Rasool Babaahmadi, Milan Pramanik, Tanja Kaehler, Ayan Dasgupta, Emma Richards, Alireza Ariafard, Thomas Wirth, Rebecca L. Melen
Publikováno v:
Dalton Transactions. 52:5039-5043
Herein we report the B(3,4,5-F3H2C6)3-catalysed C3-allylation of indoles using allylic esters.
Autor:
Omar Ouadoudi, Tanja Kaehler, Enes Görkem Çevik, Michael Bolte, Berthold Stöger, Alexander Virovets, Hans-Wolfram Lerner, Matthias Wagner
Publikováno v:
Dalton Transactions. 51:13195-13198
Regioselectively di- and tetrabrominated (B,O)2-perylenes were prepared and used in Stille-type couplings to afford highly luminescent alkynylated derivatives.
Autor:
Omar, Ouadoudi, Tanja, Kaehler, Enes Görkem, Çevik, Michael, Bolte, Berthold, Stöger, Alexander, Virovets, Hans-Wolfram, Lerner, Matthias, Wagner
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 51(35)
Regioselective di- and tetrabrominations of the (B,O)
Autor:
Tanja Kaehler, Jonas Lorenz, Darren M. C. Ould, Dorothea Engl, Micol Santi, Lukas Gierlichs, Thomas Wirth, Rebecca L. Melen
The synthesis of a series of alpha-aryl or alpha-alkyl functionalised beta-hydroxy and beta-keto esters has been achieved by reacting alpha-diazoesters with boranes, and aldehydes, ketones, anhydrides, nitriles, esters or isocyanates. In a mild react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9119975264b530f055b57e73c2821a77
https://orca.cardiff.ac.uk/id/eprint/150817/1/d2ob00643j.pdf
https://orca.cardiff.ac.uk/id/eprint/150817/1/d2ob00643j.pdf
Publikováno v:
European Journal of Organic Chemistry. 2020:5847-5851
Vicinally diiodinated polycyclic aromatic hydrocarbons (I2‐PAHs) are accessible from the corresponding diborylated B2‐PAHs through boron/iodine exchange. The B2‐PAHs have been prepared via twofold electrophilic borylation reactions templated by
Publikováno v:
Chemical Science
The isoelectronic replacement of C Created by potrace 1.16, written by Peter Selinger 2001-2019 C bonds with −BN+ bonds in polycyclic aromatic hydrocarbons (PAHs) is a widely used tool to prepare novel optoelectronic materials. Far less well explor
Autor:
Tanja Kaehler, Rebecca L. Melen
Publikováno v:
Cell Reports Physical Science. 2:100595
Summary The chemistry of Lewis acids, in particular that of triarylboranes, has received unprecedented attention in recent years. Particularly in their role as the Lewis acid component of frustrated Lewis pairs (FLPs), boranes have shown astonishing
Publikováno v:
Angewandte Chemie.
Substitutional doping of perylene with two boron atoms at the 6b/12b positions and two oxygen or nitrogen atoms at the 1/7 positions has been achieved. The modular synthesis route developed for these bis-BO- (3) and bis-BN-perylenes (5) starts from t
Publikováno v:
Organicbiomolecular chemistry. 14(24)
A Brønsted acid-catalyzed addition of 2-alkylazaarenes to in situ generated N-sulfonylimines through selective C(sp(3))-H bond functionalization has been developed. This protocol provides an atom- and step-economic approach to α-substituted sulfona