Novel synthetic methods for the preparation of nitrogen containing sulfur(VI) functionalities [PDF]
The adoption of unusual functional groups into medicinal and agrochemical research programmes provides enhanced coverage of both chemical and intellectual property space.
Briggs, Edward Lewis
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Sulfoximine‐Directed Arene ortho‐Lithiation
The growing importance of sulfoximines in medicinal chemistry has led to a renewed interest in their synthesis and functionalization. This review describes the directed ortho‐lithiation of S‐aryl sulfoximines. Discussed are the synthesis and reactivity of five different types of o‐lithiosulfoximines, including o‐lithiosulfoximines with and without α ...
Hans‐Joachim Gais
wiley +1 more source
Synthesis and Transformations of NH‐Sulfoximines
This review considered recent progress and achievements in the synthesis and transformation of NH‐sulfoximines. The development of strategies for direct and selective preparation of NH‐sulfoximines, even in enantioenriched form or by using sustainable approaches and continuous flow synthesis, are reported. Transformations of sulfoximines by N−S, N−P, N−
Michael Andresini +4 more
wiley +1 more source
Revisiting the mechanism of the Fujiwara-Moritani reaction [PDF]
The Fujiwara–Moritani reaction between p-methylacetanilide and n-butyl acrylate, catalysed by Pd(OAc)2 in the presence of toluenesulfonic acid and benzoquinone, was (re-)investigated using reaction calorimetry and complementary spectroscopic methods. The
Hii, KK, Mulligan, C, Parker, J
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Chiral Phosphoric Acids as Versatile Tools for Organocatalytic Asymmetric Transfer Hydrogenations
Organocatalytic asymmetric transfer hydrogenation provides a metal‐free and ambient alternative to classical reductions. Chiral phosphoric acid‐catalysis represents a powerful strategy in this field, with a range of novel and selective methods for various double bond reductions.
Ádám Márk Pálvölgyi +3 more
wiley +1 more source
Nature‐Inspired Functional Chromophores from Biomimetic o‐Quinone Chemistry
Bioinspired manipulation of o‐quinones generated from natural catechols represents a straightforward strategy to access the diverse molecular scaffolds endowed with peculiar functional chromophores, which offers a finely tunable palette of colors, emissions and input/output opportunities in response to pH, light, oxidant species and other external ...
Maria Laura Alfieri +4 more
wiley +1 more source
The Synthesis and Biological Evaluation of Novel Nitrogen Containing 6 and 7 Membered Ring Heterocyclic Compounds [PDF]
Literature reports have previously shown interesting antimicrobial activities of compounds containing the α,β unsaturated carbonyl function and various piperidone and tropanone derivatives have attracted interest.
Hussain, Idhnan Abas
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Abstract Three‐dimensional aza‐analogues of 1,2‐benzothiazine 1,1‐dioxides have been prepared from sulfonimidamides. Two different protocols are presented. The first is a rhodium‐catalyzed annulation reaction with α‐sulfonyloxyketones leading to 4‐unsubstituted benzothiazine derivatives.
Jan‐Hendrik Schöbel +4 more
wiley +1 more source
A promising PET tracer candidate targeting α‐synuclein inclusions
Clinical and Translational Medicine, Volume 13, Issue 9, September 2023.
Jie Xiang, Zhentao Zhang, Keqiang Ye
wiley +1 more source
Palladium-Catalyzed, Enantioselective Formal Cycloaddition between Benzyltriflamides and Allenes: Straightforward Access to Enantioenriched Isoquinolines [PDF]
Benzyl and allyltriflamides can engage in Pd-catalyzed oxidative (4+2) annulations with allenes, to produce highly valuable tetrahydroisoquinoline or dihydropyridine skeletons.
Gulías Costa, Moisés +2 more
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