Results 31 to 40 of about 5,649 (226)
Donald A. Tomalia is one of the pioneers in the field of dendrimers, who is still active at the age of 80 years-old. The present contribution is a journey through his scientific contributions from the early beginning until his discovery of the poly ...
Jørn Bolstad Christensen
doaj +1 more source
Strained Ammonium Precursors for Radiofluorinations
The increasing application of positron emission tomography (PET) in nuclear medicine has stimulated the extensive development of a multitude of novel and versatile techniques to introduce fluorine‐18, especially for the radiolabelling of biologically or ...
Dr. Falco Reissig, Dr. Constantin Mamat
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Small ring heterocycles, such as epoxides and aziridines, are present in several natural products and are also highly versatile building blocks, frequently involved in the synthesis of numerous bioactive products and pharmaceuticals.
Allan Ribeiro da Silva +3 more
doaj +1 more source
Allylic alcohols and amines by carbenoid eliminative cross-coupling using epoxides or aziridines
α-Lithiated terminal epoxides and N-(tert-butylsulfonyl)aziridines undergo eliminative cross-coupling with α-lithio ethers, to give convergent access to allylic alcohols and allylic amines, respectively.
Matthew J. Fleming, David M. Hodgson
doaj +1 more source
Silver-Catalyzed Trifluoromethoxylation of Aziridines
We disclose a silver-catalyzed trifluoromethoxylation of N-tosyl aziridines with trifluoromethyl arylsulfonate. The protocol is characterized by its mild conditions, simple operations, and good chemo- and regioselectivity.
Xiangyu Deng (5181719) +5 more
core +1 more source
Rhodium(III)-Catalyzed C-C Coupling between Arenes and Aziridines by C-H Activation
Rhodium(III)-Catalyzed C-C Coupling between Arenes and Aziridines by C-H ...
Wan, Boshun +6 more
core +1 more source
‐Sulfonyl Aziridines and Cyclic Anhydrides
We report a new synthetic methodology for poly(ester amide)s by anionic ring-opening copolymerization of N -sulfonyl aziridines and cyclic anhydrides.
Nikos Hadjichristidis +3 more
core +1 more source
Transition metal-free Csp3-Csp3 bond-forming reactions of N-tosylaziridines and gem-diborylalkanes
The incorporation of additional Csp3 atoms into candidate drugs may enhance their pharmacological properties. Nevertheless, it remains challenging to construct desired Csp3-Csp3 bonds efficiently and practically.
Pu-Zhang Zi +8 more
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Synthesis of Functionalized Arylaziridines as Potential Antimicrobial Agents
By using the Suzuki-Miyaura protocol, a simple straightforward synthesis of functionalized 2-arylaziridines has been developed. By means of this synthetic strategy from readily available ortho-, meta- and para-bromophenylaziridines and aryl- or ...
Arianna Giovine +8 more
doaj +1 more source
Funktionalisierung von Peptiden auf der festen Phase im späten Synthesestadium
Peptidmodifikationen sind für die Kontrolle der Eigenschaften von Peptidwirkstoffen von entscheidender Bedeutung. Daher sind Strategien, die einen effizienten und schnellen Einbau nicht‐kanonischer Modifikationen in Peptide in Parallelformaten ermöglichen, sehr gefragt.
Marius Werner +2 more
wiley +1 more source

