Results 31 to 40 of about 20,876 (282)

Factors affecting the extent of branching in fischertropsch synthesis products with iron-based catalysts [PDF]

open access: yes, 1989
Branched products are mainly formed during secondary isomerization reactions, and not in the main synthesis reaction itself. The extent of branching is a function of the catalyst formulation. High acidity and a low hydrogenation strength of the catalyst (
Snel, R.
core   +2 more sources

On-DNA Hydroalkylation to Introduce Diverse Bicyclo[1.1.1]pentanes and Abundant Alkyls via Halogen Atom Transfer.

open access: yesJournal of the American Chemical Society, 2022
DNA-encoded libraries have proven their tremendous value in the identification of new lead compounds for drug discovery. To access libraries in new chemical space, many methods have emerged to transpose traditional mol-scale reactivity to nmol-scale, on ...
Expédite Yen-Pon   +7 more
semanticscholar   +1 more source

Insertion of [1.1.1]propellane into aromatic disulfides

open access: yesBeilstein Journal of Organic Chemistry, 2019
Herein we present the synthesis of symmetrically and unsymmetrically substituted 1,3-bissulfanylbicyclo[1.1.1]pentanes from disulfides and [1.1.1]propellane.
Robin M. Bär   +4 more
doaj   +1 more source

Organocatalytic Vinyl and Friedel−Crafts Alkylations with Trifluoroborate Salts [PDF]

open access: yes, 2007
Herein we report the first use of vinyl and heteroaryl trifluoroborate salts as viable substrates for amine-catalyzed conjugate additions. The application of LUMO-lowering iminium catalysis has enabled the highly regio- and enantioselective 1,4-addition ...
Lee, Sandra, MacMillan, David W. C.
core   +1 more source

Bicyclo[1.1.1]pentane Embedded in Porphyrinoids** [PDF]

open access: yesAngewandte Chemie, 2023
AbstractWe report a two‐step approach to obtain synthetically versatile bicyclo[1.1.1]pentane (BCP) derivatives using Grignard reagents. This method allows the incorporation of BCP units in tetrapyrrolic macrocycles and the synthesis of a new class of calix[4]pyrrole analogues by replacing two bridging methylene groups with two BCP units.
Nitika Grover   +5 more
openaire   +4 more sources

Twofold Radical-Based Synthesis of N,C-Difunctionalized Bicyclo[1.1.1]pentanes.

open access: yesJournal of the American Chemical Society, 2021
Bicyclo[1.1.1]pentylamines (BCPAs) are of growing importance to the pharmaceutical industry as sp3-rich bioisosteres of anilines and N-tert-butyl groups.
Helena D. Pickford   +5 more
semanticscholar   +1 more source

Photochemical Formal (4 + 2)-Cycloaddition of Imine-Substituted Bicyclo[1.1.1]pentanes and Alkenes.

open access: yesJournal of the American Chemical Society, 2021
Amines containing bridged bicyclic carbon skeletons are desirable building blocks for medicinal chemistry. Herein, we report the conversion of bicyclo[1.1.1]pentan-1-amines to a wide range of polysubstituted bicyclo[3.1.1]heptan-1-amines through a ...
Alexander S. Harmata   +3 more
semanticscholar   +1 more source

Emission characteristics of nonmethane hydrocarbons from private cars and taxis at different driving speeds in Hong Kong [PDF]

open access: yes, 2011
Vehicular emissions are the major sources of a number of air pollutants including nonmethane hydrocarbons (NMHCs) in urban area. The emission composition and emission factors of NMHCs from vehicles are currently lacking in Hong Kong.
Blake, DR   +4 more
core   +1 more source

Electrophilic Activation of [1.1.1]Propellane for the Synthesis of Nitrogen‐Substituted Bicyclo[1.1.1]pentanes

open access: yesAngewandte Chemie, 2021
Strategies commonly used for the synthesis of functionalised bicyclo[1.1.1]pentanes (BCP) rely on the reaction of [1.1.1]propellane with anionic or radical intermediates.
S. Livesley   +6 more
semanticscholar   +1 more source

Strain-release transformations of bicyclo[1.1.0]butanes and [1.1.1]propellanes

open access: yesTetrahedron Chem
Bicyclo[1.1.0]butanes (BCBs) and [1.1.1]propellanes (tricyclo[1.1.1.01,3]pentanes, TCPs) are structurally unique compounds with different chemical properties.
Qian-Qian Hu   +4 more
doaj   +1 more source

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