Tritium labelled alkenes via the Shapiro reaction
暂无分享,去创建一个
[1] Chuan Yi Tang,et al. A 2.|E|-Bit Distributed Algorithm for the Directed Euler Trail Problem , 1993, Inf. Process. Lett..
[2] P. Williams,et al. Synthesis of [3H]pinoline, an endogenous tetrahydro‐ß‐carboline , 1992 .
[3] P. Williams,et al. Design and operations at the National Tritium Labelling Facility , 1991 .
[4] J. Honour,et al. Synthesis of [11,11,12,12-2H4]progesterone for mass spectral investigations of peripheral metabolism , 1990, Steroids.
[5] D. Bur,et al. Stereoselective partial hydrogenation of the triple bond in methyl 2-ethyl-6,6-dimethylhept-2-en-4-ynoate: A comparison of lindlar and montmorillonite catalysts , 1990 .
[6] R. Vogt,et al. Tritium-labeled enantiomers of disparlure. Synthesis and in vitro metabolism , 1989 .
[7] T. Baillie. Synthesis and applications of isotopically labelled compounds , 1988 .
[8] G. Prestwich. Chemistry of pheromone and hormone metabolism in insects. , 1987, Science.
[9] John R. Jones,et al. Handbook of tritium NMR spectroscopy and applications , 1985 .
[10] A. Barrett,et al. Recent applications of the Shapiro reaction , 1983 .
[11] R. DiPietro,et al. Alkylation and subsequent decomposition of arylsulfonylhydrazone dianions , 1981 .
[12] P. Rylander. Catalytic Hydrogenation in Organic Syntheses , 1979 .
[13] A. Chamberlin,et al. Leaving-group variation in aprotic Bamford-Stevens carbene generation , 1978 .
[14] A. Chamberlin,et al. Vinyllithium reagents from arenesulfonylhydrazones , 1978 .
[15] J. Stemke,et al. Efficient synthesis of deuterated olefins from arenesulfonylhydrazones , 1975 .
[16] R. Shapiro,et al. Tosylhydrazones and alkyllithium reagents: More on the regiospecificity of the reaction and the trapping of three intermediates , 1975 .
[17] R. Shapiro,et al. Mixture of mechanisms in the reaction of tosylhydrazones with alkyllithium reagents , 1974 .
[18] D. P. Dolata,et al. N,N-Ditosylhydrazones. Synthesis and some unique reactions with alkyllithium reagents , 1973 .
[19] J. Herz,et al. Reaction of some steroidal tosylhydrazones with lithium alkyls , 1970 .
[20] R. Shapiro. Tosylhydrazones IV. Stereochemistry of the reaction of tosylhydrazones with methyllithium. , 1968 .
[21] R. Shapiro,et al. Tosylhydrazones. V. Reaction of Tosylhydrazones with Alkyllithium Reagents. A New Olefin Synthesis. , 1967 .
[22] F. Cook,et al. Reactions of butyllithium with sulfonylhydrazones , 1967 .
[23] L. Caglioti,et al. The reaction of tosylhydrazones with lithium aluminium hydride , 1963 .
[24] N. L. Allinger,et al. Macro Rings. XIII. Synthesis and Properties of 1,7-Cyclododecadiyne and Related Compounds1 , 1956 .
[25] H. Lindlar. Ein neuer Katalysator für selektive Hydrierungen , 1952 .