참고문헌

1. J. Org. Chem. v.43 no.1263 E. C. Ashby;J. J. Lin
2. Tetrahedron Lett. F. Sato;Y. Mori;M. Sato
3. Chem. Rev. v.81 D. C. Bailey;S. H. Langer
4. J. Mol. Catal. v.12 T. L. Brown
5. J. C. S. Chem. Commun. H. Alper;C. Blais
6. J. Organomet. Chem. v.168 H. Alper;J. K. Currie
7. Full v.59 H. Alper;C. Blais
8. Full v.61 H. Alper;M. Gopal;J. Heveling
9. J. Org. Chem. v.40 H. Alper
10. Tetrahedron Lett. H. Alper;F. Sibtain;J. Heveling
11. Angew. Chem., Int. Ed. Engl. v.19 H. Alper;S. Ripley;T. L. Prince
12. J. Org. Chem. v.48 H. Alper;T. L. Prince
13. Tetrahedron Lett. S. C. Shim;S. Antebi;H. Alper
14. J. Org. Chem. v.50 S. C. Shim;S. Antebi;H. Alper
15. European Patent Appin., 0146 291A1 S. C. Shim;H. Alper;D.J.H.Smith
16. J. Heterocyclic. Chem. v.25 S. C. Shim;C.H.Doh;T.J.Kim;H.K.Lee;K.D.Kim
17. Transition Metal Organometalics in Organic Synthesis v.II H. Alper
18. Bull Chem. Soc. Jpn. v.49 no.1378 Y. Watanabe;S. C. Shim;T. Mitsudo;Y. Takegami
19. Tetrahedron v.42 S. C. Shim;K. T. Huh;W. H. Park
20. Inorg. Chem. v.18 D.J.Darensbourg;M.Y.Darensbourg;N.Walker;J.A.Froelich;H.L.C.Barros
21. Tetrahedron Lett. S.C.Shim;K.N.Choi