Borderline mechanisms involving ion-molecule pairs for the nucleophilic substitution reactions of benzhydrol and its derivatives. Facile formation and cleavage of diphenylmethyl ethers for the protection of hydroxyl groups

Tetrahedron Letters

Volumn 39, Issue 15, 1998, Pages 2037-2038

  Paredes, Rodrigo ^a   Pérez, Ruby L ^a  

^a UNIVERSIDAD DEL VALLE   (Colombia)

Author keywords

Benzhydryl Carbocation; Benzhydryl Group as a Protective Group for Alcohols; Intimate Ion molecule Pairs; Nucleophilic Substitution on Benzhydrol and its Derivatives

Indexed keywords

BENZHYDRYL DERIVATIVE; HYDROXYL GROUP; TOLUENESULFONIC ACID DERIVATIVE;

ARTICLE; CHEMICAL BINDING; COLUMN CHROMATOGRAPHY; ION TRANSPORT; OUTCOMES RESEARCH; REACTION ANALYSIS; TRANSPORT KINETICS;

EID: 0032499176     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00181-6     Document Type: Article

References (4)

1. 1. Paredes, R.; Agudelo, F.; Taborda, G. Tetrahedron Lett. 1996, 37, 1965-1966.
2. 2. Ohwada, T.; Shudo, K.J. J. Am. Chem. Soc. 1988, 110, 1862-1870.
3. 3. Greene, T.W. Protective Groups in Organic Synthesis. 2nd ed., Wiley: New York, 1991; p 59.
4. 4. Pratt, E. F.; Draper, J.D. J. Am. Chem. Soc. 1949, 71, 2846-2849.