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- W1569438384 abstract "This chapter discusses the monocyclic thiazines and their functionalized derivatives. The sp3-hybridized saturated carbon bearing the extra hydrogen was indicated by a number placed after those for the heteroatoms. Hence, 2H-1,3-thiazine was named 1,3,2-thiazine. The chapter discusses the synthesis of 1,3-thiazines. Type I, (3+3) synthesis is divided into a discussion of reactions carried out starting from thioamides, thioureas, substituted thioureas, dithiocarbamic acids and their ammonium salts, and miscellaneous syntheses. The physical properties of 1,3-thiazines are also discussed. The basicities of the few 1,3-thiazines studied are located between those of sodium bicarbonate and ammonia. The chemical properties are reduction reaction, reaction with nucleophiles, reaction with electrophiles, cycloadditions, side chains, and rearrangements. Electrochemical reduction of 2-phenyl-6H-l,3-thiazines is carried out at a mercury cathode in acetate buffer and ethanol (1:1). The three uses of 1,3-thiazines are also discussed. It includes: (1) medicinal applications, (2) 1, 3-thiazines as pesticides and growth factors, and (3) miscellaneous." @default.
- W1569438384 created "2016-06-24" @default.
- W1569438384 creator A5015855860 @default.
- W1569438384 creator A5027058078 @default.
- W1569438384 date "1990-01-01" @default.
- W1569438384 modified "2023-10-11" @default.
- W1569438384 title "1,3-Thiazines" @default.
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- W1569438384 doi "https://doi.org/10.1016/s0065-2725(08)60062-8" @default.
- W1569438384 hasPublicationYear "1990" @default.
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