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Recent Advances in the High-Value Conversion of Alkenes Induced by Electrochemistry [PDF]

open access: yesMolecules
Over the past few decades, electrosynthesis has advanced significantly, enabling numerous valuable transformations for synthetic chemists. Olefins are inexpensive, readily available industrial feedstocks extensively used in organic synthesis.
Xing’an Liang   +4 more
doaj   +2 more sources

Alkene Diversification through a Molecular Recasting Strategy Enabled by N-Heterocyclic Carbene and Photoredox Dual Catalysis [PDF]

open access: yesResearch
Alkenes are fundamental structural motifs in organic synthesis, valued for their prevalence in natural products and their broad reactivity profile. While traditional de novo synthesis offers access to diverse alkene frameworks, strategies enabling the ...
Qing-Zhu Li   +6 more
doaj   +2 more sources

Synthesis of a New α-Azidomethyl Styrene from Safrole via a Dearomative Rearrangement

open access: yesMolbank, 2023
There is a growing interest in developing more efficient synthetic alternatives for the synthesis of nitrogen-containing allylic compounds. This article presents a straightforward two-step protocol to produce 5-(3-azidoprop-1-en-2-yl)benzo[d][1,3]dioxole
Stephen R. Isbel, Alejandro Bugarin
doaj   +1 more source

Iodoaminations of Alkenes [PDF]

open access: yesSynthesis, 2016
The activation of alkenes and their subsequent functionalization is a frequently used methodology in synthetic chemistry. This review highlights recent iodine-mediated aminations and elaborates on the various strategies to bring about regio- or stereoselective transformations.
Wirth, Thomas, Mizar, Pushpak
openaire   +2 more sources

Asymmetric Epoxidation of Olefins with Sodium Percarbonate Catalyzed by Bis-amino-bis-pyridine Manganese Complexes

open access: yesMolecules, 2022
Asymmetric epoxidation of a series of olefinic substrates with sodium percarbonate oxidant in the presence of homogeneous catalysts based on Mn complexes with bis-amino-bis-pyridine ligands is reported.
Varvara A. Drozd   +2 more
doaj   +1 more source

Chain Propagation Mechanism of Fischer–Tropsch Synthesis: Experimental Evidence by Aldehyde, Alcohol and Alkene Addition

open access: yesReactions, 2021
Fischer–Tropsch synthesis (FTS) produces hundreds of hydrocarbons and oxygenates by simple reactants (CO + H2) and the detailed chain propagation mechanism is still in dispute.
Liping Zhou   +4 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

2-Alkylation of 3-Alkyindoles With Unactivated Alkenes

open access: yesFrontiers in Chemistry, 2022
An acid-catalyzed 2-alkylation of indole molecules is developed. Only catalytic amount of the commercially available, inexpensive and traceless HI is used as the sole reaction promoter. 2,3-Disubstituted indole molecules bearing congested tertiary carbon
Xuling Pan, Qian Liu, Yingling Nong
doaj   +1 more source

Harnessing a P450 fatty acid decarboxylase from Macrococcus caseolyticus for microbial biosynthesis of odd chain terminal alkenes

open access: yesMetabolic Engineering Communications, 2018
Alkenes are industrially important platform chemicals with broad applications. In this study, we report a direct microbial biosynthesis of terminal alkenes from fermentable sugars by harnessing a P450 fatty acid (FA) decarboxylase from Macrococcus ...
Jong-Won Lee   +2 more
doaj   +1 more source

A mild and effective method for the conversion of alkenes into alcohols in subcritical water [PDF]

open access: yesJournal of the Serbian Chemical Society, 2007
Alkenes were oxidized to alcohols in subcritical water. A number of alkenes were oxidized directly to their alcohols in excellent yields. The syntheses were performed in 215 cm3 stainless steel high pressure reactor at 120 ºC in 150 cm3 water. The yields
RECEP OZEN, NERMİN S. KUS
doaj   +3 more sources

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