Results 131 to 140 of about 32,736 (165)
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Chemischer Informationsdienst, 1986
AbstractDie Oxidation der Alkohole (I) und ihrer schneller reagierenden äquatorialen Epimeren ist bei konstanter HClO4‐Konzentration von‐ jeweils 1. Ordnung bezüglich beider Reaktionspartner und von ‐ 1. Ordnung in bezug auf das entstehende Acetamid.
M. JAMBULINGAM +7 more
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AbstractDie Oxidation der Alkohole (I) und ihrer schneller reagierenden äquatorialen Epimeren ist bei konstanter HClO4‐Konzentration von‐ jeweils 1. Ordnung bezüglich beider Reaktionspartner und von ‐ 1. Ordnung in bezug auf das entstehende Acetamid.
M. JAMBULINGAM +7 more
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Organometallics, 2018
Ruthenium(II) hydride complexes bearing a pyrazolyl-(2-indol-1-yl)-pyridine ligand were synthesized and structurally characterized by NMR analysis and X-ray single crystal crystallographic determinations. These complexes efficiently catalyzed acceptorless dehydrogenation of N-heterocycles and secondary alcohols, respectively, exhibiting highly ...
Qingfu Wang, Huining Chai, Zhengkun Yu
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Ruthenium(II) hydride complexes bearing a pyrazolyl-(2-indol-1-yl)-pyridine ligand were synthesized and structurally characterized by NMR analysis and X-ray single crystal crystallographic determinations. These complexes efficiently catalyzed acceptorless dehydrogenation of N-heterocycles and secondary alcohols, respectively, exhibiting highly ...
Qingfu Wang, Huining Chai, Zhengkun Yu
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ChemInform, 2013
AbstractThe catalyst can be recovered by simple filtration and reused eight or twelve times (β‐alkylation resp.
Dong Wang +8 more
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AbstractThe catalyst can be recovered by simple filtration and reused eight or twelve times (β‐alkylation resp.
Dong Wang +8 more
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ChemInform, 2010
AbstractThe use of 2,4‐dichlorotoluene as a solvent is crucial to shorten the reaction time from hours (in dioxane) to minutes.
Christophe Berini +4 more
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AbstractThe use of 2,4‐dichlorotoluene as a solvent is crucial to shorten the reaction time from hours (in dioxane) to minutes.
Christophe Berini +4 more
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Organometallics, 2019
Three bidentate ruthenium(II) complexes with a pyridonate fragment were prepared and fully characterized. These complexes are structurally similar, but differ in their pendant substituents. Complex 1 contains a phenyl unit, whereas complexes 2 and 3 have uncoordinated thienyl and thiazolyl groups, respectively.
Chong Zhang +4 more
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Three bidentate ruthenium(II) complexes with a pyridonate fragment were prepared and fully characterized. These complexes are structurally similar, but differ in their pendant substituents. Complex 1 contains a phenyl unit, whereas complexes 2 and 3 have uncoordinated thienyl and thiazolyl groups, respectively.
Chong Zhang +4 more
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ChemInform, 1994
AbstractChemInform 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.
K. SELVARAJ +2 more
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AbstractChemInform 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.
K. SELVARAJ +2 more
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Organometallics, 2008
A series of five different “(p-cymene)Ru(NHC)” complexes (NHC = imidazolin-2-ylidene, imidazolin-4-ylidene, and pyrazolin-3-ylidene) have been obtained and fully characterized. The crystal structure of two of the new complexes has been determined by X-ray diffraction methods.
Amparo Prades +3 more
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A series of five different “(p-cymene)Ru(NHC)” complexes (NHC = imidazolin-2-ylidene, imidazolin-4-ylidene, and pyrazolin-3-ylidene) have been obtained and fully characterized. The crystal structure of two of the new complexes has been determined by X-ray diffraction methods.
Amparo Prades +3 more
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ACS Catalysis, 2019
The direct intramolecular stereospecific substitution of the hydroxyl group in stereogenic secondary alcohols was successfully accomplished by phosphinic acid catalysis.
Anon Bunrit +7 more
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The direct intramolecular stereospecific substitution of the hydroxyl group in stereogenic secondary alcohols was successfully accomplished by phosphinic acid catalysis.
Anon Bunrit +7 more
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Organic Chemistry Frontiers
A transfer hydrogenation of aryl azides with alcohols, promoted exclusively by alkali metal bases, has been developed. This protocol enables efficient C–N bond formation and is broadly applicable to the synthesis of diverse N-heterocycles.
Jinwoo Lee +6 more
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A transfer hydrogenation of aryl azides with alcohols, promoted exclusively by alkali metal bases, has been developed. This protocol enables efficient C–N bond formation and is broadly applicable to the synthesis of diverse N-heterocycles.
Jinwoo Lee +6 more
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International Journal of Chemical Kinetics, 1994
AbstractAn investigation of the kinetics of oxidation of epimeric piperidin‐4‐ols, oxan‐4‐ols, and cyclohexanol by N‐chloro‐r‐2, c‐6‐diphenyl‐t‐3‐methylpiperidin‐4‐one (NCP) in aqueous acetic acid in the presence of perchloric acid shows that the reaction is first‐order each in substrate and oxidant.
Kuppusamy Selvaraj +2 more
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AbstractAn investigation of the kinetics of oxidation of epimeric piperidin‐4‐ols, oxan‐4‐ols, and cyclohexanol by N‐chloro‐r‐2, c‐6‐diphenyl‐t‐3‐methylpiperidin‐4‐one (NCP) in aqueous acetic acid in the presence of perchloric acid shows that the reaction is first‐order each in substrate and oxidant.
Kuppusamy Selvaraj +2 more
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