참고문헌 (18)

1. J. Am. Chem. Soc. W. C. Still 105 2487 1983 10.1021/ja00346a071 Still, W. C. and Barrish, J. C.: Stereoselective synthesis of 1,3-diol derivatives and application to the ansa bridge of rifamycin S,J. Am. Chem. Soc.,105, 2487 (1983); (b) Sharpless, K. B., Behrens, C. H., Katsuki, Lee, A. W. M., Martin, V. S., Takatain, M., Viti, M., Walker, F. J. and Woodard, S. S.: Stereo and regioselective openings of chiral 2,3-epoxy alchols. Versatile routes to optically pure natural products and drugs. Unusual kinetic resolutions.Pure & Appl. Chem.,55, 589 (1983); (c) Cha, J. K., Christ, W. J. and Kishi, Y.: On stereochemistry of osmium tetroxide oxidation of alcohol system; examples,Tetrahedron 40, 2247 (1984). 

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2. J. Am. Chem. Soc. K. Oshima 95 7926 1973 10.1021/ja00804a094 Oshima, K., Yamamoto, H. and Nozaki, H.: Carbon-carbon bond formation by selective coupling of alkylthioallycopper reagent with allylic halides,J. Am. Chem. Soc.,95, 7926 (1973); (b) Still, W. C. and MacDonald, T. L.: Allyloxy carbanion. A new synthesis of aldehydesvia a β-acyl carbanion equivalent,J. Am. Chem. Soc. 96, 5561 (1974). 

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3. Bull. Chem. Soc. Jpn. K. Oshima 48 1567 1975 10.1246/bcsj.48.1567 Oshima, K., Yamamoto, H. and Nozaki, H.: Carbon-carbon bond formation by selective coupling of alkylthioally-copper reagent with allylic halides.Bull. Chem. Soc. Jpn.,48, 1567 (1975). 

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4. Biellmann, J. F. and Cucep, J. B.: α-Alcoylation d’allyl-thioethers: Couplage queue-a-queue d’nuites 3 isopreniques,Tet. Lett., 5629 (1968). 

5. J. Am. Chem. Soc. D. A. Evans 96 5560 1974 10.1021/ja00824a039 Evans, D. A., Andrews, G. C. and Buckwalter, B.: Metalated allylic ethers as homoenolates anion equivalents,J. Am. Chem. Soc. 96, 5560 (1974). 

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6. Atlani, P. M., Biellmann, J. F., Dube, S. and Vicens, J. J.: The influence of solvation of the reactions of an allylic carbanion,Tet. Lett., 2665 (1974). 

7. 10.1246/cl.1979.385 Yamamoto, Y., Yatagai, H. and Maruyama, K.: Protonolysis of alkenylboranes under neutral conditions by treatment with catalytic amounts of palladium diacetate,Chem. Lett., 385, (1979). 

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8. J. Org. Chem. K. S. Kyler 46 5182 1981 10.1021/jo00338a024 Kyler, K. S. and Watt, D. S.: Partial syntheisis of (20R, 22R)-20, 22-dihydroxy cholesterol,J. Org. Chem.,46, 5182 (1981); (b) Kyler, K. S., Netzel, M. A., Arseniyadis, and Watt, D. S.: Conjugated addition of 1-(phenylthio)-1-(trimethylsilyl)-2-propene to unsaturated ketones,J. Org. Chem.,48, 383 (1983). 

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9. Acc. Chem. Res. D. A. Evans 7 147 1974 10.1021/ar50077a004 Evans, D. A. and Andrews, G. C.: Allylic sulfo-xides; useful intermediates in organic synthesis,Acc. Chem. Res. 7, 147 (1974). 

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10. Bull. Chem. Soc. Jpn. T. Sakai 38 381 1965 10.1246/bcsj.38.381 Sakai, T. and Hirose, Y.: The structure and stereochemistry of four new sesquiterpenes isolated from the wood oil of “kaya” (Torreya nucifera),Bull. Chem. Soc. Jpn.,38, 381 (1965). 

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11. Bull. Korea Chem. Soc. H. Park 11 167 1990 Park, H., Ham, W. H., Suh, K. H. and Kim, S. J.: Reaction of thioallylic carbanion withR-glyceraldehyde,Bull. Korea Chem. Soc.,11, 167 (1990). 

12. J. Am. Chem. Soc. H. T. Clarke 55 4571 1933 10.1021/ja01338a041 Clarke, H. T., Gillespie, H. B. and Weisshaus, S. Z.: The action of formalehyde on amine and amino acids,J. Am. Chem. Soc.,55, 4571 (1933). 

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13. Saniere-Karila, M., Capmau, M. L. and Chodkiewicz, W.: Stereochemistry of the addition of organometallics of 3-bromobutyne to carbonyl derivatives,Bull. Soc. Chim. Fr., 3371 (1973); (b) Favre, E. and Gaudemar, M.: Reactivity of dibutyl propargyl-and allenyl boronates in comparison to carbonyl derivatives III. Stereochemistry of the condensation of aldehdes,J. Organomet. Chem. 92, 17 (1975). 

14. J. Org. Chem. Y. Yamamoto 45 195 1980 10.1021/jo01289a050 Yamamoto, Y., Yatagai, H. and Maruyama, K.: High control of the regiochemistry in reactions of heterosubstituted allylic carbanionsvia allylic aluminum “Ate” complex.J. Org. Chem. 45, 195 (1980). 

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15. Bull. Chem. Soc. Jpn. Y. Ikeda 57 2781 1984 10.1246/bcsj.57.2781 Ikeda, Y., Ikeda, N. and Yamamoto, H.: Selective synthesis of [3-(alkylthio)allyl] titanium reagent with carbonyl compounds.Bull. Chem. Soc. Jpn.,57, 2781 (1984); (b) Ikeda, Y. and Yamamoto, H.: A practical synthesis of 1,3-diene using allyltriphenylsilane and titanium tetraisopropoxide,Bull. Chem. Soc. Jpn.,59, 657 (1986); (c) Ikeda, Y., Ukai, J., Ikeda, N. and Yamamoto, H.: Stereoselective synthesis of 1,4-disubstituted 1,3-diene from aldehyde using organotitanium reagent,Tetrahedron 43, 731 (1987). 

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16. J. Am. Chem. Soc. G. Stork 75 384 1953 10.1021/ja01098a039 Stork, G., Tamelen, E. E. V., Friedmann, L. J. and Burgstahler, A. W.: A stereospecific synthesis of cantharidin,J. Am. Chem. Soc. 75, 384 (1953). 

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17. J. Am. Chem. Soc. H. Akins 70 695 1948 10.1021/ja01182a080 Akins, H. and Billica, H. R.: The preparation of Raney nickel catalysts and their use under conditions comparable with those for platinum and palladium catalysts,J. Am. Chem. Soc. 70, 695 (1948). 

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18. J. Am. Chem. Soc. J. A. Dale 90 3732 1968 10.1021/ja01016a024 Dale, J. A. and Mosher, H. S.: Nuclear magnetic resonance nonequivalence of diastereomeric esters of α-substituted phenylacetic acids for the determination of stereochemical purity,J. Am. Chem. Soc.,90, 3732 (1968); (b) Dale, J. A., Dull, D. L. and Mosher, H. S.: α-methyl-α-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines,J. Org. Chem.,34, 2543 (1969); (c) Hub, L. and Mosher, H. S.: α-methyl-α-trifluoromethylophenylacetic acid. Configuration by asymetric synthesis,J. Org. Chem 35, 3691 (1970); (d) Dale, J. A. and Mosher, H. S.: Nuclear magnetic resonance entiomer reagent. Configuration correlationvia nuclear magnetic resonance chemical shifts of diastereomeric mandelate and α-methoxy-α-trifluoromethylphenylacetate (MTPA) esters.J. Am. Chem. Soc. 95, 512 (1973). 

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