Results 201 to 210 of about 13,292 (250)
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ChemInform Abstract: Reaction of Nitrones with Trimethylsilylketene.
ChemInform, 1999AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Kiyo Takaoka +2 more
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Studies on conjugated nitrones: addition of hydrogen cyanide on to conjugated nitrones
Journal of the Chemical Society D: Chemical Communications, 1969The elements of hydrogen cyanide and of methanol add in a 1,3-manner to conjugated nitrones.
Nazar Singh, S. Mohan
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The Reactions of Nitrones with Indoles
Tetrahedron, 2000AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Helene Chalaya‐Mauger +3 more
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ChemInform Abstract: Nucleophilic Perfluoroalkylation of Nitrones.
ChemInform, 1999AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Beniamin N. V. Pintea +2 more
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Nitrones. 7. .alpha.-Quinoxalinyl-N-substituted nitrone 1,4-dioxides
Journal of Medicinal Chemistry, 1977A series of alpha-quinoxalinyl-N-substitute nitrone 1,4-dioxides has been synthesize and evaluated as antibacterial and antiprotozoal agents. Structure-activity relationships are discussed. Of the compounds tested, alpha-(3-methyl-2-quinoxalinyl)-N-methylnitrone 1,4-dioxide (2) was the most active agent in vivo against the gram-negative and the gram ...
Hyun Koo Kim +3 more
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Cycloadditions of chiral nitrones
J. Chem. Soc., Chem. Commun., 1977AbstractAus den chiralen Nitronen (I) entstehen mit den Olefinen (II) die Addukte (III), mit Phenylisocyanat (IV) analog die Oxadi‐ ′azolidinone (V).
Irma Panfil, Czeslaw Belzecki
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Trimethylaluminum‐Assisted Alkynylation of Nitrones.
ChemInform, 2007AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Tanasri Bunlaksananusorn +2 more
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Correlation between structure and stability of nitronic acids and nitronic esters
Science in China Series B: Chemistry, 1998On the basis of investigation on structural characteristics and stability of more than one hundred nitronic acids and nitronic esters, an equilibrium theory of electronic effects in conjugated systems is put forward and the type of structures is classified. On that basis, an empirical rule for the correlation between structure and stability of nitronic
Chenglie Yin, Fu’an Kang
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The Cycloaddition of Nitrones with Homochiral Cyclopropanes
The Journal of Organic Chemistry, 2007AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Katarina Sapeta, Michael A. Kerr
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Organic Letters, 2018 
The rhodium(III)-catalyzed cross-coupling of (hetero)aryl nitrones with Morita-Baylis-Hillman (MBH) adducts is described. An allylated intermediate derived from aryl nitrones and MBH adducts allows the formation of bridged cyclic compounds via an exotype
A. Pandey +8 more
semanticscholar +1 more source
The rhodium(III)-catalyzed cross-coupling of (hetero)aryl nitrones with Morita-Baylis-Hillman (MBH) adducts is described. An allylated intermediate derived from aryl nitrones and MBH adducts allows the formation of bridged cyclic compounds via an exotype
A. Pandey +8 more
semanticscholar +1 more source

