Volume 19, Issue 33
Preparative Organic Chemistry
Full Access

ChemInform Abstract: Fused Sulfolanes. Part 1. Synthesis and Rearrangement of trans-2-Iminoperhydrothieno(3,4-d)oxazol-5,5-dioxides.

T. E. BEZMENOVA

T. E. BEZMENOVA

Otd. neftekhim. inst. fiz.-org. khim. i uglekhim. AN Ukr. SSR, Kiev 252160

Search for more papers by this author
A. B. ROZHENKO

A. B. ROZHENKO

Otd. neftekhim. inst. fiz.-org. khim. i uglekhim. AN Ukr. SSR, Kiev 252160

Search for more papers by this author
G. I. KHASKIN

G. I. KHASKIN

Otd. neftekhim. inst. fiz.-org. khim. i uglekhim. AN Ukr. SSR, Kiev 252160

Search for more papers by this author
A. G. BRATUNETS

A. G. BRATUNETS

Otd. neftekhim. inst. fiz.-org. khim. i uglekhim. AN Ukr. SSR, Kiev 252160

Search for more papers by this author
A. M. SHAKHVOROST

A. M. SHAKHVOROST

Otd. neftekhim. inst. fiz.-org. khim. i uglekhim. AN Ukr. SSR, Kiev 252160

Search for more papers by this author
First published: August 16, 1988

Abstract

The aminohydroxysulfolane (I) reacts with the isothiocyanates (II) to give the corresponding thioureas which are cyclized in situ, producing the iminooxazoles (III).

ChemInform Abstract

The aminohydroxysulfolane (I) reacts with the isothiocyanates (II) to give the corresponding thioureas which are cyclized in situ, producing the iminooxazoles (III). Basic treatment of (IIIa) - (IIId) yields the rearranged imidazolones (IVa) - (IVd). (IVa) and (IVc) are also prepared from (Va) or (Vc) and cyanogen bromide (VI).

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.