Results 1 to 10 of about 29,164 (249)
Recent Advances in the High-Value Conversion of Alkenes Induced by Electrochemistry [PDF]
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
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Synthesis of a New α-Azidomethyl Styrene from Safrole via a Dearomative Rearrangement
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
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Iodoaminations of Alkenes [PDF]
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
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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
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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
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Alkene-oxo and alkene-alkene coupling on Pt(II) [PDF]
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
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
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Synthetic Studies on Erythromycin Derivatives: Reactivity of the C12-21 Alkene
The reactivity of the C12-21 alkene of some erythromycin A derivatives was studied. This double bond was easily oxidized to the corresponding epoxide with excellent stereoselectivity. A single crystal X-ray structure showed that the epoxide moiety was on
Wei-Min Chen
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2-Alkylation of 3-Alkyindoles With Unactivated Alkenes
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
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Conventional frontier molecular orbital theory is not able to satisfactorily explain the regioselectivity outcome of the nitrilimine–alkene cycloaddition.
Giorgio Molteni, Alessandro Ponti
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