Optisch aktive Carbodiimide

Zetzsche, Fritz; Fredrich, Artur

doi:10.1002/cber.19400731016

Cited by 31 publications

(15 citation statements)

References 8 publications

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“…The extension of the reaction to involve the symmetrical diarylthiourea derivatives instead of the dialkyl derivatives in the former reaction (1,3-diphenyl-, 1,3-di-p-tolyl- and 1,3-di-p-chlorophenylthioureas) in CHCl 3 under various reaction conditions (at 60 °C for 6 h, at room temperature for 6 days or in the presence of triethylamine for 2 h) gave the quinazoline derivatives 10 . The reaction pathway could be either the decomposition of diaryl thiourea to aniline and the respective aryl isothiocyanate [ 7 ]. The reaction of 1 with anilines to give 10 confirmed both the structure of the quinazoline derivative and this possible reaction pathway.…”

Section: Resultsmentioning

confidence: 99%

Synthesis of Heterocyclic Skeletons by the Reaction of N1-(2-Cyanophenyl)-benzimidoyl Chloride with Thioamides

Fathalla

Pazdera

2002

Molecules

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Section: Resultsmentioning

confidence: 99%

Synthesis of Heterocyclic Skeletons by the Reaction of N1-(2-Cyanophenyl)-benzimidoyl Chloride with Thioamides

Fathalla

Pazdera

2002

Molecules

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“…(7) Reaction of isocyanide dichlorides with primary amine hydrochlorides in an inert solvent at 180°C [71]. (8) Reaction of N-substituted trichlorophosphazenes with phenyl isocyanate [72].…”

Section: Miscellaneous Methodsmentioning

confidence: 99%

“…The earliest preparations of carbodiimides involved the reaction of mercuric or lead oxide with thioureas [6][7][8][9][10].…”

Section: Introductionmentioning

confidence: 99%

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Carbodiimides

1971

Organic Chemistry: A Series of Monographs

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“…At dilutions greater than 1 : 100,000, neither phenylazoapocupreine nor its ethyl ether showed power against the pneumococcus.~ Miura found no protective action with small doses of 5'-amino-8'-(sulfamidophenylazo)-ethylhydrocupreine (80). The 5'-amino group of aminodihydroquinine and aminooptochin has recently been used for the preparation of mustard oils (115) ; these derivatives have no antimalarial action.…”

Section: Substitution In the Quinoline Ring Of The Cinchona: Nitromentioning

confidence: 99%

Structure and Antipneumococcic Activity in the Cinchona Series.

Renfrew¹,

Cretcher²

1942

Chem. Rev.

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The present survey gives particular emphasis to recent studies of the antipneumococcic action of some cinchona derivatives. A brief historical survey is presented and reference is made to speculations concerning the mode of action of cinchonas in the animal body. Antipneumococcic action is analyzed with regard to isomeric and structural modifications of the cinchona molecule. A summary of recent data on bacteriostasis, toxicity, animal protection, pharmacologic testing, and clinical studies is given. Synthetic analogs are discussed in relation to significant structural factors.Cinchona alkaloids have been used as antimalarials since 1630, but evidence of the specific antipneumococcic action of these compounds dates only from 1911. RIorgenroth's (84) study of cinchonas as antipneumococcic agents has been described as "the first striking instance of the successful application of a chemical to the treatment of a bacterial infection in a laboratory animal" (53). Because Morgenroth had been studying quinine in relation to trypanosome infections in animals and was acquainted with the capsule-formation characteristic of trypanosomes, spirilla, and the pneumococcus, he was led to investigate the action of the alkaloid in pneumococcic septicemia in mice. There followed an extensive study of hydrocupreine ethers with the synthesis of the well-known optochin, vuein, and eucupin. Between 1919 and 1924 Heidelberger and Jacobs (42, 54) a t the Rockefeller Institute and Giemsa (32, 33) in Germany published the results of further studies in the hydrocupreine series. These results have been reviewed by von Oettingen (111) and by Houben (50), and the clinical findings have been discussed by Moore and Chesney (87), by Kolmer (63), and by Solis-Cohen (107).The remarkable antipneumococcic action of optochin has been a spur to reinvestigation of this field. In again studying cinchona derivatives the search was not so much for a compound of greater power but rather for a compound free from deleterious side-effects. The last decade has brought extensive synthesis in the field of apocinchonas. In the early 1930's methylapocupreinel [or 1 At the time the term apocupreine (8) was suggested, its use was based firstly on the similarities of apocupreine (formula 11) and cupreine (formula I), which differ chemically only in the 3-substituent of ethylidene or vinyl, respectively, and secondly on the established usage of Leger (59, 66) in applying the terms apocinchonine and apocinchonidine (characterized by the ethylidene side chain) to the corresponding substances derived from cinchonine and cinchonidine. In the case of quinine, demethylation is accomplished by boiling with 60 per cent sulfuric acid; a shift of the double bond also occurs. The product, called apoquinine by Hesse (49), consists of substances of different toxicities and antipneumococcic powers and these give derivatives of various biological properties. The name 49

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Optisch aktive Carbodiimide

Cited by 31 publications

References 8 publications

Synthesis of Heterocyclic Skeletons by the Reaction of N1-(2-Cyanophenyl)-benzimidoyl Chloride with Thioamides

Synthesis of Heterocyclic Skeletons by the Reaction of N1-(2-Cyanophenyl)-benzimidoyl Chloride with Thioamides

Carbodiimides

Structure and Antipneumococcic Activity in the Cinchona Series.

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