Articles with "alder cycloaddition" as a keyword



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The reactivity enhancement in Diels–Alder cycloaddition of 1,3-diene by cation encapsulation to C60: a computational insight

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Published in 2020 at "Structural Chemistry"

DOI: 10.1007/s11224-020-01538-4

Abstract: The origin of the experimentally known preference for [6,6] bonds in cycloaddition reactions involving C60 has been computationally explored. To this end, we examined the reactions of 1,3-dienes with fullerene (C60) in the context of… read more here.

Keywords: diels alder; reactivity enhancement; enhancement diels; reactivity ... See more keywords
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Synthesis of 4,5,6,7-tetrahydrobenzoxazol-2-ones by a highly regioselective Diels-Alder cycloaddition of exo-oxazolidin-2-one dienes with chalcones

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Published in 2019 at "Tetrahedron Letters"

DOI: 10.1016/j.tetlet.2019.04.027

Abstract: Abstract The synthesis of novel of 4,5,6,7-tetrahydrobenzoxazol-2-ones is herein reported. They were obtained in moderate to good yields by a highly regio- and stereoselective Diels-Alder cycloaddition of N-substituted exo-oxazolidin-2-one dienes with chalcones or bis-chalcones as… read more here.

Keywords: oxazolidin one; one dienes; alder cycloaddition; exo oxazolidin ... See more keywords
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Rapid Access to the Structural Core of Aflavinines via Stereoselective Tandem Intramolecular Diels-Alder Cycloaddition Controlled by the Allylic 1,3-Strain.

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Published in 2019 at "Organic letters"

DOI: 10.1021/acs.orglett.9b02457

Abstract: An expedient route to access the functionalized structural core of aflavinines has been developed starting from three readily available fragments over 12 steps in 29.1% overall yield without using any transition metal catalysis. The key… read more here.

Keywords: tandem intramolecular; diels alder; core aflavinines; structural core ... See more keywords
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Design of Surface-Aligned Main-Chain Liquid-Crystal Networks Prepared under Ambient, Light-Free Conditions Using the Diels-Alder Cycloaddition.

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Published in 2022 at "ACS macro letters"

DOI: 10.1021/acsmacrolett.2c00616

Abstract: Surface-aligned liquid-crystal networks (LCNs) offer a solution for developing functional materials capable of performing a range of tasks, including actuation, shape memory, and surfaces patterning. Here we show that Diels-Alder cycloaddition can be used to… read more here.

Keywords: liquid crystal; diels alder; alder cycloaddition; surface aligned ... See more keywords
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A mechanistic study on cationic Li prompted Diels–Alder cycloaddition of cycloparaphenylene

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Published in 2017 at "Organic chemistry frontiers"

DOI: 10.1039/c7qo00290d

Abstract: We introduce Li+ involving cycloadditions between acetylene and ring-like cycloparaphenylenes (CPPs) in theory. Orbital analysis suggests an inverse electron-demand mechanism in which the diene CPP acts as an electron acceptor. Partial electron transfer to Li+… read more here.

Keywords: diels alder; cationic prompted; study cationic; mechanistic study ... See more keywords
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Desilicated ZSM-5 Zeolites for the Production of Renewable p-Xylene via Diels-Alder Cycloaddition of Dimethylfuran and Ethylene

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Published in 2018 at "Catalysts"

DOI: 10.3390/catal8060253

Abstract: The selective production of p-xylene and other aromatics starting from sugars and bioderived ethylene offers great promise and can eliminate the need for separation of xylene isomers, as well as decreasing dependency on fossil resources… read more here.

Keywords: diels alder; production; xylene; alder cycloaddition ... See more keywords
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Diels–Alder Cycloaddition to the Bay Region of Perylene and Its Derivatives as an Attractive Strategy for PAH Core Expansion: Theoretical and Practical Aspects

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Published in 2020 at "Molecules"

DOI: 10.3390/molecules25225373

Abstract: PAHs (polycyclic aromatics hydrocarbons), the compound group that contains perylene and its derivatives, including functionalized ones, have attracted a great deal of interest in many fields of science and modern technology. This review presents all… read more here.

Keywords: cycloaddition; diels alder; perylene derivatives; strategy ... See more keywords