Results 1 to 10 of about 195,903 (365)

Effect of polarity and steric on the rate addition of free radicals to Alkenes [PDF]

open access: diamondKirkuk Journal of Science, 2009
In this investigation, the effective factors on the addition rate for hydroxy methyl and cynomethyl free radicals to some alkenes have been studied using quantum mechanics methods. Where in this study, physical properties like the electron density on the
Najla.J. Khalil, Mostafa.R. Aeyd
doaj   +2 more sources

Photocatalytic hydrofluoroalkylation of alkenes with carboxylic acids [PDF]

open access: greenNature Chemistry, 2023
Kang‐Jie Bian   +5 more
openalex   +2 more sources

Metallaphotoredox-enabled aminocarboxylation of alkenes with CO_2

open access: yesNature Catalysis, 2023
The conversion of CO_2 to valuable chemicals is highly desirable for sustainable development. Among the various methods available, the difunctionalizing carboxylation of alkenes with CO_2 emerges as an exceptionally efficient approach that facilitates ...
Jun-Ping Yue   +8 more
semanticscholar   +1 more source

Metal-free visible-light-enabled vicinal trifluoromethyl dithiolation of unactivated alkenes

open access: yesBeilstein Journal of Organic Chemistry, 2021
The difunctionalization of alkenes involving a trifluoromethylthio group (SCF3) for the conversion of versatile and readily available olefins into structurally more complex molecules has been successfully studied.
Xiaojuan Li   +5 more
doaj   +1 more source

Synthesis of Dibenzylbutane and 9,8′-Neo-Lignans via Cyclometalation of Allylbenzene by EtAlCl2 and Mg in the Presence of Zr ansa-Complexes

open access: yesChemistry Proceedings, 2021
The aim of the research is the development of a one-pot method for the synthesis of lignans, natural compounds that show a wide spectrum of biological activities.
Pavel V. Kovyazin   +3 more
doaj   +1 more source

Photoexcited nitroarenes for the oxidative cleavage of alkenes

open access: yesNature, 2022
The oxidative cleavage of alkenes is an integral process that converts feedstock materials into high-value synthetic intermediates1–3. The most viable method to achieve this in one chemical step is with ozone4–7; however, this poses technical and safety ...
A. Ruffoni   +3 more
semanticscholar   +1 more source

Nickel-Catalyzed Dicarbofunctionalization of Alkenes.

open access: yesACS Catalysis, 2020
1,2-Dicarbofunctionalization of alkenes has emerged as an efficient synthetic strategy for preparing substituted molecules by coupling readily available alkenes with electrophiles and/or nucleophiles.
Xiaoxu Qi, Tianning Diao
semanticscholar   +2 more sources

Metal-Free Photochemical Imino-Alkylation of Alkenes with Bifunctional Oxime Esters.

open access: yesJournal of the American Chemical Society, 2022
The concurrent installation of C-C and C-N bonds across alkene frameworks represents a powerful tool to prepare motifs that are ubiquitous in pharmaceuticals and bioactive compounds.
Jadab Majhi   +7 more
semanticscholar   +1 more source

From‐Neutral‐to‐Neutral Reductive Radical Coupling of Non‐Activated Alcohols and Styrenes

open access: yesChemistryEurope, 2023
A reductive radical coupling reaction between non‐activated aliphatic alcohols and styrenes has been discovered through the use of low‐valent Ti‐mediated C−O bond homolysis.
Dr. Takuya Suga   +2 more
doaj   +1 more source

Alkene-oxo and alkene-alkene coupling on Pt(II) [PDF]

open access: yes, 2021
Tetranuclear Pt(II) oxo-complex [(COD)4Pt4([mu]3-O)2Cl2](BF4)2 (1) (COD = 1,5- cyclooctadiene) was found to readily react with a variety of alkenes (ethylene, norbornene, propylene and cyclopentene). The most significant discovery resulted from the norbornene reaction, which gave platinaoxetane [(COD)2Pt2(OC7H10)Cl]BF4 (4), the first metallaoxetane ...
openaire   +2 more sources

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