Synthesis and hydrolysis of monocarbamate from allylic 1,4-dicarbamate: Bis-homodichloroinositol

The efficient synthesis of a new class of allylic cis/trans-dicarbamates are described. Allylic diols as key intermediates of the targeted compounds were prepared in a facile way, starting from p-benzoquinone. Reaction of allylic diol compounds with p-TsNCO resulted in the formation of cis/trans-dicarbamate groups. The structure of cis/trans-dicarbamates were determined by 1H-NMR, 13C-NMR, FT-IR and elemental analysis techniques.

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Synthesis and hydrolysis of monocarbamate from allylic 1,4-dicarbamate: Bis-homodichloroinositol

Cited by 3 publications

References 71 publications

Concise synthesis of chloro-benzoconduritols via effect of acetyl chloride (AcCl): Mattocks type reaction

Concise synthesis of chloro-benzoconduritols via effect of acetyl chloride (AcCl): Mattocks type reaction

Stereospecific synthesis of Pd(0)-catalyzed oxazolidinone with tetracyclic structure

Stereospecific Synthesis of cis/trans-dicarbamates

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