Results 1 to 10 of about 25,247 (120)

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

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

Trifluoromethanesulfonamide vs. Non-Fluorinated Sulfonamides in Oxidative Sulfamidation of the C=C Bond: An In Silico Study

open access: yesMolecules, 2020
A theoretical analysis of the reaction of oxidative sulfamidation of several alkenes was performed in order to explain the various experimental observations and different reactivity of triflamide and non-fluorinated sulfonamides.
Anton V. Kuzmin   +2 more
doaj   +1 more source

Iron(III)-Mediated Rapid Radical-Type Three-Component Deuteration of Quinoxalinones With Olefins and NaBD4

open access: yesFrontiers in Chemistry, 2020
Iron(III)-promoted rapid three-component deuteration of quinoxalinones with olefins and NaBD4 is reported for the first time, which provides a novel, economic, and efficient method for the rapid synthesis of deuterated quinoxalinones.
Wanmei Li   +6 more
doaj   +1 more source

Iodine-Mediated Alkoxyselenylation of Alkenes and Dienes with Elemental Selenium

open access: yesMolecules, 2022
A one-pot synthesis of linear and cyclic β-alkoxyselenides is developed through the iodine-mediated three-component reaction of elemental selenium with alkenes (dienes) and alcohols.
Evgeny O. Kurkutov, Bagrat A. Shainyan
doaj   +1 more source

Chemical Composition of Essential Oil from Four Sympatric Orchids in NW-Italy

open access: yesPlants, 2022
Orchidaceae is a flowering plant family worldwide distributed known for producing volatile organic compounds (VOCs) which can act as olfactory signals for pollinators.
Francesco Saverio Robustelli della Cuna   +5 more
doaj   +1 more source

Enantioselective Hydrogenations with Chiral Titanocenes

open access: yesMolecules, 2005
In this review article chiral titanocenes and their application for the enantioselective hydrogenations of different unsaturated compounds are discussed, with a special emphasis on the kinetics and the practicality of the developed systems. The nature of
J. Khinast, A. Panarello, O. Vassylyev
doaj   +1 more source

Regioselective One-Pot Synthesis of Novel Functionalized Organoselenium Compound by Bis-Alkoxyselenenylation of Alkenes with Selenium Dibromide and Alcohols

open access: yesInorganics, 2022
The one-pot efficient synthesis of novel functionalized organoselenium compound by bis-alkoxyselenenylation of alkenes with selenium dibromide and alcohols was developed.
Vladimir A. Potapov   +6 more
doaj   +1 more source

Efficient Regioselective Synthesis of Novel Condensed Sulfur–Nitrogen Heterocyclic Compounds Based on Annulation Reactions of 2-Quinolinesulfenyl Halides with Alkenes and Cycloalkenes

open access: yesMolecules, 2021
The preparation of novel reagents 2-quinolinesulfenyl chloride and bromide based on available 2-mercaptoquinoline has been described. This approach opens up opportunities for the introduction of 2-quinolinesulfenyl chloride and bromide into organic ...
Vladimir A. Potapov   +2 more
doaj   +1 more source

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