Nuclear magnetic resonance studies of the mechanism of keto-enol tautomerism in 3-hydroxy-2,4-dimethylcyclobutenone. II. Solvent and pH effects

James S. Chickos; Rudolph Ernst K. Winter

doi:10.1021/ja00783a033

Nuclear magnetic resonance studies of the mechanism of keto-enol tautomerism in 3-hydroxy-2,4-dimethylcyclobutenone. II. Solvent and pH effects

James S. Chickos, Rudolph Ernst K. Winter

University of Missouri-St. Louis

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

Original language	American English
Journal	Journal of the American Chemical Society
Volume	95
DOIs	https://doi.org/10.1021/ja00783a033
State	Published - Jan 1 1973

Disciplines

Organic Chemistry
Inorganic Chemistry
Chemistry

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title = "Nuclear magnetic resonance studies of the mechanism of keto-enol tautomerism in 3-hydroxy-2,4-dimethylcyclobutenone. II. Solvent and pH effects",

author = "Chickos, \{James S.\} and Winter, \{Rudolph Ernst K.\}",

year = "1973",

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day = "1",

doi = "10.1021/ja00783a033",

language = "American English",

volume = "95",

journal = "Journal of the American Chemical Society",

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TY - JOUR

T1 - Nuclear magnetic resonance studies of the mechanism of keto-enol tautomerism in 3-hydroxy-2,4-dimethylcyclobutenone. II. Solvent and pH effects

AU - Chickos, James S.

AU - Winter, Rudolph Ernst K.

PY - 1973/1/1

Y1 - 1973/1/1

UR - http://pubs.acs.org/doi/abs/10.1021/ja00783a033

U2 - 10.1021/ja00783a033

DO - 10.1021/ja00783a033

M3 - Article

VL - 95

JO - Journal of the American Chemical Society

JF - Journal of the American Chemical Society

ER -

Nuclear magnetic resonance studies of the mechanism of keto-enol tautomerism in 3-hydroxy-2,4-dimethylcyclobutenone. II. Solvent and pH effects

Disciplines

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