Studies in claisen rearrangement—II
暂无分享,去创建一个
[1] B. Burreson,et al. Influence of Alkyl Groups on the Rate of the para Claisen Rearrangement , 1965 .
[2] W. J. L. Noble,et al. The Formation of 2,4-Dimethoxy-6-methylphenylacetone from 3,5-Dimethoxybenzyl isopropenyl Ether. A New Variant of the Claisen Rearrangement , 1964 .
[3] T. Padmanathan,et al. 796. Unsaturated systems. Part IV. The ortho-Claisen rearrangement of α- and γ-aryloxy-β-methylcrotonates and α-phenoxy-γ-methylcrotonate , 1963 .
[4] W. N. White,et al. The ortho-Claisen Rearrangement. VI. The Rates of Rearrangement of Allyl m-X-Phenyl Ethers to 2-Allyl-5-X-phenols1 , 1962 .
[5] W. N. White,et al. The ortho-Claisen Rearrangement. V. The Products of Rearrangement of Allyl m-X-Phenyl Ethers1 , 1961 .
[6] W. K. Fife,et al. The ortho-Claisen Rearrangement. IV. The Rearrangement of X-Cinnamyl p-Tolyl Ethers1 , 1961 .
[7] W. K. Fife,et al. Communications. The Electronic Nature of the Transition State of the Claisen Rearrangement. , 1961 .
[8] W. K. Fife,et al. The ortho-Claisen Rearrangement. I. The Effect of Substituents on the Rearrangement of Allyl p-X-Phenyl Ethers1,2 , 1958 .
[9] R. Jacobson,et al. A Kinetic Study of the ortho-Claisen Rearrangement1 , 1958 .
[10] H. Zaugg,et al. Muscle-relaxing Compounds Derived from 1,4-Dichloro-2-butene1 , 1957 .
[11] W. Bailey,et al. Acetylenes. I. Mixed Dihalides and Halohydrins from Butynediol1 , 1955 .
[12] R. Gaertner. An “Isoaromatic” Product from 2-Methyl-3-benzofurylmethylmagnesium Chloride , 1952 .
[13] R. Gaertner. The Equilibrium between the o-Allenylphenoxide and 2-Benzofurylmethyl Anions , 1951 .
[14] H. Nozaki,et al. The Preparation of Synthetic Estrogens. IV.1Condensation of Biacetyl with Phenols , 1949 .
[15] E. Tietze,et al. Über den Mechanismus der Umlagerung der Phenol‐allyläther. (2. Mitteilung) , 1926 .
[16] R. Adams,et al. CYCLIC ETHERS FROM o-ALLYL PHENOLS; METHYLENE COUMARANES. , 1919 .
[17] L. Claisen. Über Umlagerung von Phenol-allyläthern in C-Allyl-phenole , 1912 .