Reaction of acylisothiocyanates with 5-isopropoxy-4-methyloxazole

Reaction of Acylisothiocyanates with 5-Isopropoxy-4-methyloxazole.-It is shown for the first time that 5-acylimino-3-thiazoline derivatives such as (III) are formed by formal [3 + 2] cycloaddition of the carbonsulfur double bond of acylisocyanates (II) to the oxazole ring in (I) in moderate to good yields. The structure of compound (IIIa) is confirmed by X-ray diffraction analysis. -(DUDIN, A. V.; AGAFONOV, N. E.; ZHULIN, V. M.; Mendeleev Commun.

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ChemInform Abstract: Reaction of Acylisothiocyanates with 5‐Isopropoxy‐4‐methyloxazole.

Dudin

Agafonov

Zhulin

1998

ChemInform

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Reaction of acylisothiocyanates with 5-isopropoxy-4-methyloxazole

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ChemInform Abstract: Reaction of Acylisothiocyanates with 5‐Isopropoxy‐4‐methyloxazole.

ChemInform Abstract: Reaction of Acylisothiocyanates with 5‐Isopropoxy‐4‐methyloxazole.

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