Asymmetric Synthesis in the Oxymercuration Reaction Using Optically Active Mercuric Salts
- 1 August 1974
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 47 (8) , 1945-1947
- https://doi.org/10.1246/bcsj.47.1945
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Solvomercuration-demercuration. I. Oxymercuration-demercuration of representative olefins in an aqueous system. Mild procedure for the Markovnikov hydration of the carbon-carbon double bondThe Journal of Organic Chemistry, 1970
- Solvomercuration-demercuration of representative olefins in the presence of alcohols. Convenient procedures for the synthesis of ethersJournal of the American Chemical Society, 1969
- Asymmetric Synthesis with Sugar Derivatives. II. Asymmetric Syntheses by Methoxy-Mercuration of Cinnamic Esters of Sugar DerivativesBulletin of the Chemical Society of Japan, 1967
- Asymmetric Synthesis in the Methoxy-mercuration of α, β-Unsaturated EstersBulletin of the Chemical Society of Japan, 1967
- Six-Coördinate Mercury(II)Inorganic Chemistry, 1962
- A Calorimetric Determination of the Values of ΔH° for Mercury(II)-Halide Complex Ion Reactions and the Derived Values of ΔS0 1,2a,bJournal of the American Chemical Society, 1960
- Methoxymercuration of CyclohexeneJournal of the American Chemical Society, 1947
- CERTAIN REACTIONS OF THE ALKYL AND ARYL MERCURIC HYDROXIDESJournal of the American Chemical Society, 1924
- Über die optischaktiven Monomethylester der WeinsäurenEuropean Journal of Inorganic Chemistry, 1909