Alkaline Hydrolysis of Nonphenolic β-0-4 Model Diastereomers: Substituent Effect on the Leaving Phenoxide
- 1 January 1998
- journal article
- research article
- Published by Walter de Gruyter GmbH in Holzforschung
- Vol. 52 (2) , 171-174
- https://doi.org/10.1515/hfsg.1998.52.2.171
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Stereoselective Synthesis of Threo 1-(3,4-Dimethoxyphenyl)-2-(2-methoxyphenoxy)-propan-1 -olHolzforschung, 1997
- Alkaline Hydrolysis of Nonphenolic ß-O-4 Lignin Model Dimers: Further Studies of the Substituent Effect on the Leaving PhenoxideHolzforschung, 1996
- Alkaline Hydrolysis of Nonphenolic ß—O—4 Lignin Model Dimers: Substituent Effects on the Leaving Phenoxide in Neighboring Group vs Direct Nucleophilic AttackHolzforschung, 1992
- Kinetics of Alkaline Cleavage of β-Aryl Ether Bonds in Lignin Models: Significance to DelignificationHolzforschung, 1983
- Zum alkalischen Abbau der p-Alkoxy-arylglycerin-beta-arylätherstrukturen des Lignins. Versuche mit erythro-Veratrylglycerin-beta-guajacyläther.Acta Chemica Scandinavica, 1972
- Zur Spaltung von beta-Hydroxy-alkyl-aryläthern durch Alkali. II. Der stereochemische Verlauf.Acta Chemica Scandinavica, 1962