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4,818 Newest Publications about the topic organic chemistryrss
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29-Jun-2018 | Riveiros, Ricardo ; Tato, Rubén ; Pérez Sestelo, José ; Sarandeses, Luis A., Molecules, 2018
Molecules, Vol. 23, Pages 1582: Triorganoindium Reagents in Rh-Catalyzed C–H Activation/C–C Cross-Coupling Reactions of 2-Arylpyridines Molecules doi: 10.3390/molecules23071582 Authors: Ricardo Riveiros Rubén Tato José Pérez Sestelo Luis A. Sarandeses The activation of ...
26-Jun-2018 | Deevi Basavaiah; Ram Tilak Naganaboina, New Journal of Chemistry, 2018
This review describes, in brief, the philosophy, vision and long research experience of the senior author (DB) in the area of Baylis-Hillman (BH) [also known as Morita-Baylis-Hillman (MBH)] reaction. It presents a clear picture how the senior author (DB) has, i) uncovered BH reaction which was ...
22-Jun-2018 | Sacha Vignieri; Jesse Smith; Jake Yeston, Science , 2018
Organic Chemistry The trifluoromethanesulfonyl (Tf) group is remarkably adept at stabilizing negative charge: It boasts highly withdrawing fluorines and sulfur-oxygen bonds that can delocalize electrons through resonance. Höfler et al. took full advantage of these properties in generating a
05-Jun-2018 | Renana Gershoni-Poranne; Anuja P. Rahalkar; Amnon Stanger, Physical Chemistry Chemical Physics, 2018
Aromaticity is a central and ubiquitous concept in organic chemistry, and is used extensively to explain various phenomena. Yet, aromaticity cannot be observed or measured as a property in its own right and, to date, only qualitative and semi-quantitative relationships have been described between ...
01-Jun-2018 | Caroline Ash; Jake Yeston, Science , 2018
Organic Chemistry Insertion of palladium into an aryl halide bond is the first step in numerous variants of cross-coupling chemistry used to make carbon-carbon bonds. Copper is an appealing alternative catalyst for such reactions because of its abundance and downstream reactivity profile. However,
27-May-2018 | Kevin Hung; Xirui Hu; Thomas J. Maimone, Natural Product Reports, 2018
Covering: 2011–2017 Radical cyclizations have a rich history in organic chemistry and have been particularly generous to the field of natural product synthesis. Owing to their ability to operate in highly congested molecular quarters, and with significant functional group compatibility, ...
27-May-2018 | Geetha S. Remya; Cherumuttathu H. Suresh, New Journal of Chemistry, 2018
The relevance of substituent effects in the design and development of novel molecules has considerable interest in many industrial and synthetic reactions in organic chemistry. Molecular electrostatic potential (MESP) parameters are found to be excellent descriptors for characterizing the ...
27-May-2018 | Jun Xuan; Xia Cao; Xiao Cheng, Chemical Communication, 2018
Heterocyclic compounds are widely found in many natural isolates and medicinally relevant compounds, as well as some fine chemicals. The development of general and efficient methods for the construction of heterocyclic compounds is one of the most important tasks in synthetic organic chemistry. ...
26-May-2018 | Duncan K. Brownsey; Evgueni Gorobets; Darren J. Derksen, Organic & Biomolecular Chemistry, 2018
The utilization of unactivated substrates in annulation reactions provides access to complex products without the need for subsequent removal of the activating group. Vinylcyclopropanes (VCPs), occurring naturally in several monoterpene natural products, are an important building block for ...
26-May-2018 | Achim Link; Christof Sparr, Chemical Society Reviews, 2018
While aromatic hydrocarbons are ubiquitous in organic chemistry, they are typically not associated with chirality and stereoisomerism. Due to the planarity and symmetry of simple arenes, methods to assemble aromatic rings are not routinely considered for the stereoselective synthesis of chiral ...