Stereochemistry of the reaction of D(positive)-2,3-epoxybutane with alcohols. The coordination reaction between silver ion and alkynes. Some relationships of sterols to plant growth
PART I. The reaction between D(+)-2,3-epoxybutane and alcohols is accompanied by a Walden inversion. The 3-methoxy-2-butanol prepared in this manner is an erythro-isomer, for meso-2,3-dimethoxybutane can be prepared from it by the Williamson synthesis. PART II. Permanganate oxidation under...
Similar Items
-
The stereochemistry of elimination reactions
by: Clarke, J. R. P.
Published: (1963) -
Ring-Opening Polymerization of 1,2-epoxybutane and Application in Gasoline Additive
by: Wu, Jeng-Jaw, et al.
Published: (1999) -
Transition metal ion catalysed alkyne cyclisation reactions
by: Yang, Ting
Published: (2009) -
Stereochemistry of Bucherer and Strecker reactions
by: Jitrangsri, Chote
Published: (1974) -
The stereochemistry of the preparation and reactions of allylsilanes
by: Terrett, N. K.
Published: (1984)