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Titlebook: Synthesis of Heterocyclic Compounds; A. L. Mndzhoian Book 1959 Springer-Verlag US 1959 Alkaloid.alkaloids.biology.chemistry.cyclic compoun

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书目名称Synthesis of Heterocyclic Compounds
编辑A. L. Mndzhoian
视频video
图书封面Titlebook: Synthesis of Heterocyclic Compounds;  A. L. Mndzhoian Book 1959 Springer-Verlag US 1959 Alkaloid.alkaloids.biology.chemistry.cyclic compoun
描述The chemistry of heterocyclic compounds now forms one of the most extensive and important branches of organic chemistry. The rapid expansion of investigation in this field is due largely to the ever increasing practical importance of heterocyclic com­ pounds. The present stage in the development of organic chemistry and closely allied branches of biology is characterized by extensive investigation of physiologically active substances encountered in the plant and animal world and playing important parts in the life processes of micro- and macro-organisms. This extensive inves­ tigation of alkaloids, vitamins, hormones, antibiotics and their synthetic substitutes, and also of substances that control the bio­ chemical processes of the nervous system, has acted as a powerful stimulus to the further development of the chemistry of hetero­ cyclic compounds. Moreover, there are many well known applications of heterocyclic compounds in the manufacture of dyes, synthetic resins, synthetic rubbers, and other important materials. In response to growing demands, several monographs and treatises on the chemistry of heterocyclic compounds have appeared in recent years, the most comprehensive of
出版日期Book 1959
关键词Alkaloid; alkaloids; biology; chemistry; cyclic compound; development; heterocyclic compound; heterocyclic
版次1
doihttps://doi.org/10.1007/978-1-4757-6658-5
isbn_ebook978-1-4757-6658-5
copyrightSpringer-Verlag US 1959
The information of publication is updating

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5-Bromo-2-Furoic Acid,o absorb hydrogen bromide liberated in the reaction, the top of the condenser was connected to a Tishchenko vessel containing a solution of alkali. A mixture of 112 g (1 mole) of 2-furoic acid (see p. 43), m.p. 128–132°, 10 g of dry red phosphorus, and 800 ml of chloroform was prepared in the flask.
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5-(Diethylaminomethyl) Furfuryl Alcohol,ise over a period of 0.5–1 hour to a stirred ethereal solution (200 ml) of lithium aluminum hydride (Note 1) contained in a 500-ml three-necked flask fitted with mercury-sealed stirrer, dropping funnel, and reflux condenser protected by a calcium chloride tube.
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Methyl 5-Benzyl-2-Furoate,-ml three-necked round-bottomed flask fitted with mercury-sealed stirrer and reflux condenser protected by a calcium chloride tube, and it was stirred and cooled with ice water for two hours while 40 g (0.3 mole) of anhydrous aluminum chloride was added in small portions. When the vigorous reaction
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Methyl 5-(Diethylaminomethyl)-2-Furoate,l round-bottomed flask fitted with reflux condenser and dropping funnel. The solution was cooled with ice water, and a solution of 14.6 g (0.2 mole) of diethylamine in 30 ml of dry benzene was added over a period of ten minutes.
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