Results 151 to 160 of about 78,399 (204)

A Modular Synthesis of C5‐Sulfenyl Thiazoles via an Intermolecular Pummerer Rearrangement: An Underexplored Scaffold for Medicinal Chemistry

Angewandte Chemie, EarlyView.
Modular access to underexplored C5‐sulfenyl thiazoles via an intermolecular Pummerer rearrangement is reported. The methodology exhibits a broad functional group tolerance enabling the seamless design of trisubstituted thiazole cores bearing a sulfur handle for further elaboration.
Joe L. Smy, Theo C. Webb, Barnaby W. Greenland, S. Mark Roe, John Spencer, Storm Hassell‐Hart   +5 more
wiley   +1 more source

Editorial: Beyond borders: exploring diverse roles of heterocyclic compounds in combatting infections and cancer. [PDF]

Front Chem
Shaik AB, Bhandare RR, Rahman MM, Dua K.
europepmc   +1 more source

Influence of Substitution on the Interplay of Photochemical Switching and Phase Transitions in Azobenzene‐Based Molecular Materials

Angewandte Chemie, EarlyView.
This study investigates the influence of several substituents at different positions on photochemical and thermal properties of azobenzene‐based materials to provide valuable structure‐property relationships for the specific design of azobenzene‐based materials for future energy storage and phase change materials. ABSTRACT Understanding and translating
Conrad Averdunk, Hermann A. Wegner
wiley   +1 more source

The Application of Green Solvents in the Synthesis of S-Heterocyclic Compounds-A Review. [PDF]

Int J Mol Sci
Kosmalski T, Kołodziejska R, Przybysz M, Szeleszczuk Ł, Pawluk H, Mądra-Gackowska K, Studzińska R.   +6 more
europepmc   +1 more source

Adaptive Hydrogenation of Alkynes Using CO as a Molecular Trigger to Selectively Produce Alkanes or Z‐Alkenes

Angewandte Chemie, EarlyView.
One catalyst for two products: CO acts as a molecular trigger for adaptive alkyne hydrogenation using supported Pd nanoparticles. The catalyst reversibly switches between the formation of alkanes under H2 and Z‐alkenes under H2/CO for 37 structurally diverse alkynes.
Manisha Durai, Lachlan Sharp‐Bucknall, Tim Alexander Schubert, Jacob Johny, John‐Tommes Krzeslack, Walid Hetaba, Walter Leitner, Alexis Bordet   +7 more
wiley   +1 more source

Synthesis and Evaluation of Boron-Containing Heterocyclic Compounds with Antimicrobial and Anticancer Activities. [PDF]

Molecules
Prates JLB, de Matos Silva S, Medina-Alarcón KP, Dos Santos KS, Belizario JA, Lopes JR, Marin-Dett FH, Campos DL, Mendes Giannini MJS, Fusco-Almeida AM, Barbugli PA, Pavan FR, Dos Santos JL.   +12 more
europepmc   +1 more source

TADF‐Active Tetrazole Luminophores for Visible‐Light Functionalization of Nanoparticles and Surfaces

Angewandte Chemie, EarlyView.
A series of tetrazoles are reported that undergo 1,3‐dipolar cycloadditions with alkene and alkyne substrates, generating (dihydro)pyrazole products that exhibit thermally activated delayed fluorescence (TADF). The “photo‐click” reactivity of these tetrazoles is leveraged to functionalize nanoparticles and surfaces with TADF‐active chromophores ...
Ryoga Hojo, Katrina Bergmann, Siyuan L. Xie, Connor S. Durfy, William L. Primrose, Athan T. Gogoulis, Seja A. Elgadi, Mitchell J. Demchuk, Thomas Kalab, Peiqi Hu, Eva M. Nichols, Zachary M. Hudson   +11 more
wiley   +1 more source

Novel Heterocyclic Compounds for Treating Huntington's Disease. [PDF]

ACS Med Chem Lett
Sabnis RW, Sabnis AR.
europepmc   +1 more source

Modular Access to α‐Tertiary Amines: Electrochemical Tandem Di‐Functionalization of Olefins With Ammonia Surrogates and Amino Acids

Angewandte Chemie, EarlyView.
A metal‐ and oxidant‐free electrochemical multicomponent di‐functionalization strategy that rapidly converts 1,1‐disubstituted alkenes into α‐tertiary primary amines with simultaneous installation of bio‐relevant sulfur or selenium motifs was devised for late‐stage functionalization. ABSTRACT Quaternary carbon centers, especially those bearing nitrogen,
Adrija Ghosh, Tarun, Sven Erik Peters, Lutz Ackermann, Debasis Banerjee   +4 more
wiley   +1 more source

Nitrogen Radical Photocatalysed Reduction of Nitrous Oxide

Angewandte Chemie, EarlyView.
This work offers the first example of reduction of the potent greenhouse gas N2O to the benign products N2 and O(Bpin)2 using a nitrogen‐based catalyst. The active catalyst is shown to be a nitrogen‐based radical which operates under photocatalytic conditions.
Reece Lister‐Roberts, Agamemnon E. Crumpton, Meera Mehta   +2 more
wiley   +1 more source