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11.
It has been shown that 1-aryl-8-(4-bromophenyl)-4,6-dioxo-2H(phenyl)-7-phenyl-1,4,6,7,8,9-hexahydropyrimido[4,5-b][1,6]naphthyridines are formed on heating anilides of 1-aryl-7-(4-bromostyryl)-4-oxo-1,4-dihydropyrido[2,3-d]pyrimidine-6-carboxylic acids in PPA.__________Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, 597–600, April, 2005. 相似文献
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K. Bogdanowicz-Szwed M. Krasodomska A. Skonecka 《Monatshefte für Chemie / Chemical Monthly》1994,125(4):441-449
Summary 2-Arylidene-cyclohexanone1, -cyclopentanone2, -1-indanone3 and-1-tetralone4 react with acetoacetanilide5 yielding 2-oxo-4-aryl-3-carboxylic acid anilides derivatives of naphthalene7, indene8, fluorene9 and phenanthrene10. Reaction of1 and3 with benzoylacetanilide6 yields the corresponding Michael adducts11 and12.
Reaktion von CH-Säuren mit 2-Arylidencycloalkanonen. Synthese von -Ketosäureanilid-Derivaten von Naphthalin, Inden, Fluoren und Phenanthren
Zusammenfassung 2-Arylidencyclohexanone1, -cyclopentanone2, -1-indanone3 und -1-tetralone4 reagieren mit Acetoacetanilid5 unter Bildung von 2-Oxo-4-aryl-3-carbonsäureanilid-Derivaten von Naphthalin7, Inden8, Fluoren9 und Phenanthren10. Die Reaktion von1 und3 mit Benzoylacetanilid6 ergibt die entsprechenden Michael-Addukte11 und12.相似文献
13.
I. V. Ukrainets E. V. Mospanova N. L. Bereznyakova O. I. Naboka 《Chemistry of Heterocyclic Compounds》2007,43(12):1532-1539
Two methods are discussed and the synthesis of a series of 1-hydroxy-3-oxo-5,6-dihydro-3H-pyrrolo[3,2,1-ij]quinoline-2-carboxylic
acid anilides has been carried out. The antitubercular activity and the effect on the urinary function of the kidney have
been studied for the compounds prepared. A structure-biological activity relationship is discussed.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1808–1819, December, 2007. 相似文献
14.
Dr. Kun Liu Xiangfei Wu Dr. S. B. Jennifer Kan Dr. Seiji Shirakawa Prof. Dr. Keiji Maruoka 《化学:亚洲杂志》2013,8(12):3214-3221
Catalytic asymmetric synthesis of axially chiral o‐iodoanilides and o‐tert‐butylanilides as useful chiral building blocks was achieved by means of binaphthyl‐modified chiral quaternary ammonium‐salt‐catalyzed N‐alkylations under phase‐transfer conditions. The synthetic utility of axially chiral products was demonstrated in various transformations. For example, axially chiral N‐allyl‐o‐iodoanilide was transformed to 3‐methylindoline by means of radical cyclization with high chirality transfer from axial chirality to C‐centered chirality. Furthermore, stereochemical information on axial chirality in o‐tert‐butylanilides could be used as a template to control the stereochemistry of subsequent transformations. The transition‐state structure of the present phase‐transfer reaction was discussed on the basis of the X‐ray crystal structure of ammonium anilide, which was prepared from binaphthyl‐modified chiral ammonium bromide and o‐iodoanilide. The chiral tetraalkylammonium bromide as a phase‐transfer catalyst recognized the steric difference between the ortho substituents on anilide to obtain high enantioselectivity. The size and structural effects of the ortho substituents on anilide were investigated, and a wide variety of axially chiral anilides that possess various functional groups could be synthesized with high enantioselectivities. This method is the only general way to access a variety of axially chiral anilides in a highly enantioselective fashion reported to date. 相似文献
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Inside Cover: Rhodium(III)‐Catalyzed Tandem [2+2+2] Annulation–Lactamization of Anilides with Two Alkynoates via Cleavage of Two Adjacent C−H or C−H/C−O bonds (Chem. Asian J. 16/2016)
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19.
A. B. Deyanov M. E. Konshin Z. N. Semenova 《Chemistry of Heterocyclic Compounds》2004,40(12):1560-1563
Heating anilides (hydrazides) of 5-cyano-6-oxo-2-styrylnicotinic acids in polyphosphoric acid (PPA) leads to amides of 7-aryl-2,5-dioxo-6-phenyl(amino)-1,2,5,6,7,8-hexahydro-1,6-naphthyridine-3-carboxylic acids, which on heating with perchloric acid in acetic acid give the corresponding acids.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1809–1812, December, 2004.For Part 15 see [1]. 相似文献
20.
Oxidative Olefination of Anilides with Unactivated Alkenes Catalyzed by an (Electron‐Deficient η5‐Cyclopentadienyl)Rhodium(III) Complex Under Ambient Conditions
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Yuji Takahama Dr. Yu Shibata Prof. Dr. Ken Tanaka 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(25):9053-9056
The oxidative olefination of sp2 C?H bonds of anilides with both activated and unactivated alkenes using an (electron‐deficient η5‐cyclopentadienyl)rhodium(III) complex is reported. In contrast to reactions using this electron‐deficient rhodium(III) catalyst, [Cp*RhCl2]2 showed no activity against olefination with unactivated alkenes. In addition, the deuterium kinetic isotope effect (DKIE) study revealed that the C?H bond cleavage step is thought to be the turnover‐limiting step. 相似文献