Ring-chain isomeric transformations of 5-hydroxytetrahydrofuran-3-spiro-2′-(1′,3′-dithiolanes),-2′-(benzo-1,3-dithiolene), and -2′-(1′,3′-oxathiolane)

I. D. Kalikhman; O. B. Bannikova; V. N. Elokhina; A. S. Nakhmanovich; M. G. Voronkov

doi:10.1007/BF00503550

Ring-chain isomeric transformations of 5-hydroxytetrahydrofuran-3-spiro-2′-(1′,3′-dithiolanes),-2′-(benzo-1,3-dithiolene), and -2′-(1′,3′-oxathiolane)

I. D. Kalikhman, O. B. Bannikova, V. N. Elokhina, A. S. Nakhmanovich, M. G. Voronkov

Research output: Contribution to journal › Article › peer-review

Abstract

The ring-chain tautomerism of spiro derivatives of 5-hydroxytetrahydrofuran was investigated by PMR spectroscopy. The position of the tautomeric equilibrium and the time required to establish it depend on the nature of the solvent, the temperature, and the substituents in the tetrahydrofuran ring.

Original language	English
Pages (from-to)	355-357
Number of pages	3
Journal	Chemistry of Heterocyclic Compounds
Volume	18
Issue number	4
DOIs	https://doi.org/10.1007/BF00503550
State	Published - 1 Apr 1982
Externally published	Yes

ASJC Scopus subject areas

Organic Chemistry

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@article{3136e110593b463aab39243812a7eb77,

title = "Ring-chain isomeric transformations of 5-hydroxytetrahydrofuran-3-spiro-2′-(1′,3′-dithiolanes),-2′-(benzo-1,3-dithiolene), and -2′-(1′,3′-oxathiolane)",

abstract = "The ring-chain tautomerism of spiro derivatives of 5-hydroxytetrahydrofuran was investigated by PMR spectroscopy. The position of the tautomeric equilibrium and the time required to establish it depend on the nature of the solvent, the temperature, and the substituents in the tetrahydrofuran ring.",

author = "Kalikhman, {I. D.} and Bannikova, {O. B.} and Elokhina, {V. N.} and Nakhmanovich, {A. S.} and Voronkov, {M. G.}",

year = "1982",

month = apr,

day = "1",

doi = "10.1007/BF00503550",

language = "English",

volume = "18",

pages = "355--357",

journal = "Chemistry of Heterocyclic Compounds",

issn = "0009-3122",

publisher = "Springer New York",

number = "4",

}

Ring-chain isomeric transformations of 5-hydroxytetrahydrofuran-3-spiro-2′-(1′,3′-dithiolanes),-2′-(benzo-1,3-dithiolene), and -2′-(1′,3′-oxathiolane). / Kalikhman, I. D.; Bannikova, O. B.; Elokhina, V. N. et al.
In: Chemistry of Heterocyclic Compounds, Vol. 18, No. 4, 01.04.1982, p. 355-357.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Ring-chain isomeric transformations of 5-hydroxytetrahydrofuran-3-spiro-2′-(1′,3′-dithiolanes),-2′-(benzo-1,3-dithiolene), and -2′-(1′,3′-oxathiolane)

AU - Kalikhman, I. D.

AU - Bannikova, O. B.

AU - Elokhina, V. N.

AU - Nakhmanovich, A. S.

AU - Voronkov, M. G.

PY - 1982/4/1

Y1 - 1982/4/1

N2 - The ring-chain tautomerism of spiro derivatives of 5-hydroxytetrahydrofuran was investigated by PMR spectroscopy. The position of the tautomeric equilibrium and the time required to establish it depend on the nature of the solvent, the temperature, and the substituents in the tetrahydrofuran ring.

AB - The ring-chain tautomerism of spiro derivatives of 5-hydroxytetrahydrofuran was investigated by PMR spectroscopy. The position of the tautomeric equilibrium and the time required to establish it depend on the nature of the solvent, the temperature, and the substituents in the tetrahydrofuran ring.

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U2 - 10.1007/BF00503550

DO - 10.1007/BF00503550

M3 - Article

AN - SCOPUS:34250234780

SN - 0009-3122

VL - 18

SP - 355

EP - 357

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

IS - 4

ER -

Ring-chain isomeric transformations of 5-hydroxytetrahydrofuran-3-spiro-2′-(1′,3′-dithiolanes),-2′-(benzo-1,3-dithiolene), and -2′-(1′,3′-oxathiolane)

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