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Volumn 1996, Issue 7, 1996, Pages 600-608

Synthesis and Reactions of the Intermediates of the Wittig, Peterson, and their Related Reactions

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EID: 0001578466     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1996-5540     Document Type: Article
Times cited : (72)

References (64)
  • 1
    • 0001191706 scopus 로고
    • Barton, D. H. R.; Ollis, W. D., Eds.; Pergamon: Oxford
    • (a) Smith, D. J. H. In Comprehensive Organic Chemistry, Vol. 2; Barton, D. H. R.; Ollis, W. D., Eds.; Pergamon: Oxford, 1979; pp 1316-1329.
    • (1979) Comprehensive Organic Chemistry , vol.2 , pp. 1316-1329
    • Smith, D.J.H.1
  • 5
    • 0004068133 scopus 로고
    • Academic Press: London
    • Pelter, A; Smith, K.; Brown, H. C. Borane Reagents, Academic Press: London, 1988, pp 338-339; Pelter, A.; Smith, K. In Comprehensive Organic Synthesis: Selectivity, Strategy, and Efficiency in Modern Synthetic Chemistry; Trost, B. M.; Fleming, I., Eds.; Pergamon: Oxford, 1991, Vol. 1, Chapter 2.2, pp 487-503; Pelter, A. Pure Appl. Chem. 1994, 66, 223.
    • (1988) Borane Reagents , pp. 338-339
    • Pelter, A.1    Smith, K.2    Brown, H.C.3
  • 7
    • 0000970256 scopus 로고
    • Pelter, A; Smith, K.; Brown, H. C. Borane Reagents, Academic Press: London, 1988, pp 338-339; Pelter, A.; Smith, K. In Comprehensive Organic Synthesis: Selectivity, Strategy, and Efficiency in Modern Synthetic Chemistry; Trost, B. M.; Fleming, I., Eds.; Pergamon: Oxford, 1991, Vol. 1, Chapter 2.2, pp 487-503; Pelter, A. Pure Appl. Chem. 1994, 66, 223.
    • (1994) Pure Appl. Chem. , vol.66 , pp. 223
    • Pelter, A.1
  • 15
    • 0000593213 scopus 로고
    • Johnson, A. W.; LaCount, R. B. J. Am. Chem. Soc. 1961, 83, 417. Corey, E. J.; Chaykovsky, M. J. Am. Chem. Soc. 1962, 84, 3782. Aubé, J. In Comprehensive Organic Synthesis: Selectivity, Strategy, and Efficiency in Modern Synthetic Chemsitry, Vol. 1. Chap. 3.2; Trost, B. M.; Fleming, I., Eds; Pergamon: Oxford, 1991; pp 822-825.
    • (1961) J. Am. Chem. Soc. , vol.83 , pp. 417
    • Johnson, A.W.1    LaCount, R.B.2
  • 16
    • 0000977173 scopus 로고
    • Johnson, A. W.; LaCount, R. B. J. Am. Chem. Soc. 1961, 83, 417. Corey, E. J.; Chaykovsky, M. J. Am. Chem. Soc. 1962, 84, 3782. Aubé, J. In Comprehensive Organic Synthesis: Selectivity, Strategy, and Efficiency in Modern Synthetic Chemsitry, Vol. 1. Chap. 3.2; Trost, B. M.; Fleming, I., Eds; Pergamon: Oxford, 1991; pp 822-825.
    • (1962) J. Am. Chem. Soc. , vol.84 , pp. 3782
    • Corey, E.J.1    Chaykovsky, M.2
  • 18
    • 33845375469 scopus 로고
    • Reitz, A. B.; Nortey, S. O.; Jordan, A. D., Jr.; Mutter, M. S.; Maryanoff, B. E. J. Org. Chem. 1986, 51, 3302. Maryanoff, B. E.; Reitz, A. B.; Mutter, M. S.; Inners, R. R.; Almond, H. R., Jr.; Whittle, R. R.; Olofson, R. A. J. Am. Chem. Soc. 1986, 108, 7664. Vedejs, E.; Marth, C. F.; Ruggeri, R. J. Am. Chem. Soc. 1988, 110, 3940.
    • (1986) J. Org. Chem. , vol.51 , pp. 3302
    • Reitz, A.B.1    Nortey, S.O.2    Jordan Jr., A.D.3    Mutter, M.S.4    Maryanoff, B.E.5
  • 20
    • 0000380744 scopus 로고
    • Reitz, A. B.; Nortey, S. O.; Jordan, A. D., Jr.; Mutter, M. S.; Maryanoff, B. E. J. Org. Chem. 1986, 51, 3302. Maryanoff, B. E.; Reitz, A. B.; Mutter, M. S.; Inners, R. R.; Almond, H. R., Jr.; Whittle, R. R.; Olofson, R. A. J. Am. Chem. Soc. 1986, 108, 7664. Vedejs, E.; Marth, C. F.; Ruggeri, R. J. Am. Chem. Soc. 1988, 110, 3940.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 3940
    • Vedejs, E.1    Marth, C.F.2    Ruggeri, R.3
  • 21
    • 0347966626 scopus 로고
    • Several isolable pentacoordinate 1,2-oxaphosphetanes have been reported, but their synthetic method is limited to the reaction of phosphorus ylides with carbonyl compounds, see: Brium, G. H.; Matthews, C. N. J. Chem. Soc., Chem. Commun. 1967, 137. Ramirez, F.; Smith, C. P.; Pilot, J. F. J. Am. Chem. Soc. 1968, 90, 6726. Aly, H. A. E.; Barlow, J. H.; Russell, D. R.; Smith, D. J. H.; Swindles, M.; Trippett, S. J. Chem. Soc., Chem. Commun. 1976, 449. Bestmann, H. J.; Roth, K.; Wilheim, E.; Böhme, R.; Burzlaff, H. Angew. Chem., Int. Ed. Engl. 1979, 18, 876. Saalfrank, R. W.; Paul, W.; Liebenow, H. Angew. Chem., Int. Ed. Engl. 1980, 19, 713. Trishin, J. G.; Konovalova, I. V.; Burangulova, R. N.; Burnaeva, L. A.; Chistokletov, V. N.; Pudovik, A. N .Tetrahedron Lett. 1989, 30, 577. Huang, Y.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1991, 113, 7800. Huang, Y.; Sopchik, A. E.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1993, 115, 4031.
    • (1967) J. Chem. Soc., Chem. Commun. , pp. 137
    • Brium, G.H.1    Matthews, C.N.2
  • 22
    • 0000477519 scopus 로고
    • Several isolable pentacoordinate 1,2-oxaphosphetanes have been reported, but their synthetic method is limited to the reaction of phosphorus ylides with carbonyl compounds, see: Brium, G. H.; Matthews, C. N. J. Chem. Soc., Chem. Commun. 1967, 137. Ramirez, F.; Smith, C. P.; Pilot, J. F. J. Am. Chem. Soc. 1968, 90, 6726. Aly, H. A. E.; Barlow, J. H.; Russell, D. R.; Smith, D. J. H.; Swindles, M.; Trippett, S. J. Chem. Soc., Chem. Commun. 1976, 449. Bestmann, H. J.; Roth, K.; Wilheim, E.; Böhme, R.; Burzlaff, H. Angew. Chem., Int. Ed. Engl. 1979, 18, 876. Saalfrank, R. W.; Paul, W.; Liebenow, H. Angew. Chem., Int. Ed. Engl. 1980, 19, 713. Trishin, J. G.; Konovalova, I. V.; Burangulova, R. N.; Burnaeva, L. A.; Chistokletov, V. N.; Pudovik, A. N .Tetrahedron Lett. 1989, 30, 577. Huang, Y.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1991, 113, 7800. Huang, Y.; Sopchik, A. E.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1993, 115, 4031.
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 6726
    • Ramirez, F.1    Smith, C.P.2    Pilot, J.F.3
  • 23
    • 37049105220 scopus 로고
    • Several isolable pentacoordinate 1,2-oxaphosphetanes have been reported, but their synthetic method is limited to the reaction of phosphorus ylides with carbonyl compounds, see: Brium, G. H.; Matthews, C. N. J. Chem. Soc., Chem. Commun. 1967, 137. Ramirez, F.; Smith, C. P.; Pilot, J. F. J. Am. Chem. Soc. 1968, 90, 6726. Aly, H. A. E.; Barlow, J. H.; Russell, D. R.; Smith, D. J. H.; Swindles, M.; Trippett, S. J. Chem. Soc., Chem. Commun. 1976, 449. Bestmann, H. J.; Roth, K.; Wilheim, E.; Böhme, R.; Burzlaff, H. Angew. Chem., Int. Ed. Engl. 1979, 18, 876. Saalfrank, R. W.; Paul, W.; Liebenow, H. Angew. Chem., Int. Ed. Engl. 1980, 19, 713. Trishin, J. G.; Konovalova, I. V.; Burangulova, R. N.; Burnaeva, L. A.; Chistokletov, V. N.; Pudovik, A. N .Tetrahedron Lett. 1989, 30, 577. Huang, Y.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1991, 113, 7800. Huang, Y.; Sopchik, A. E.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1993, 115, 4031.
    • (1976) J. Chem. Soc., Chem. Commun. , pp. 449
    • Aly, H.A.E.1    Barlow, J.H.2    Russell, D.R.3    Smith, D.J.H.4    Swindles, M.5    Trippett, S.6
  • 24
    • 84985561665 scopus 로고
    • Several isolable pentacoordinate 1,2-oxaphosphetanes have been reported, but their synthetic method is limited to the reaction of phosphorus ylides with carbonyl compounds, see: Brium, G. H.; Matthews, C. N. J. Chem. Soc., Chem. Commun. 1967, 137. Ramirez, F.; Smith, C. P.; Pilot, J. F. J. Am. Chem. Soc. 1968, 90, 6726. Aly, H. A. E.; Barlow, J. H.; Russell, D. R.; Smith, D. J. H.; Swindles, M.; Trippett, S. J. Chem. Soc., Chem. Commun. 1976, 449. Bestmann, H. J.; Roth, K.; Wilheim, E.; Böhme, R.; Burzlaff, H. Angew. Chem., Int. Ed. Engl. 1979, 18, 876. Saalfrank, R. W.; Paul, W.; Liebenow, H. Angew. Chem., Int. Ed. Engl. 1980, 19, 713. Trishin, J. G.; Konovalova, I. V.; Burangulova, R. N.; Burnaeva, L. A.; Chistokletov, V. N.; Pudovik, A. N .Tetrahedron Lett. 1989, 30, 577. Huang, Y.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1991, 113, 7800. Huang, Y.; Sopchik, A. E.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1993, 115, 4031.
    • (1979) Angew. Chem., Int. Ed. Engl. , vol.18 , pp. 876
    • Bestmann, H.J.1    Roth, K.2    Wilheim, E.3    Böhme, R.4    Burzlaff, H.5
  • 25
    • 84985633543 scopus 로고
    • Several isolable pentacoordinate 1,2-oxaphosphetanes have been reported, but their synthetic method is limited to the reaction of phosphorus ylides with carbonyl compounds, see: Brium, G. H.; Matthews, C. N. J. Chem. Soc., Chem. Commun. 1967, 137. Ramirez, F.; Smith, C. P.; Pilot, J. F. J. Am. Chem. Soc. 1968, 90, 6726. Aly, H. A. E.; Barlow, J. H.; Russell, D. R.; Smith, D. J. H.; Swindles, M.; Trippett, S. J. Chem. Soc., Chem. Commun. 1976, 449. Bestmann, H. J.; Roth, K.; Wilheim, E.; Böhme, R.; Burzlaff, H. Angew. Chem., Int. Ed. Engl. 1979, 18, 876. Saalfrank, R. W.; Paul, W.; Liebenow, H. Angew. Chem., Int. Ed. Engl. 1980, 19, 713. Trishin, J. G.; Konovalova, I. V.; Burangulova, R. N.; Burnaeva, L. A.; Chistokletov, V. N.; Pudovik, A. N .Tetrahedron Lett. 1989, 30, 577. Huang, Y.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1991, 113, 7800. Huang, Y.; Sopchik, A. E.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1993, 115, 4031.
    • (1980) Angew. Chem., Int. Ed. Engl. , vol.19 , pp. 713
    • Saalfrank, R.W.1    Paul, W.2    Liebenow, H.3
  • 26
    • 0346075233 scopus 로고
    • Several isolable pentacoordinate 1,2-oxaphosphetanes have been reported, but their synthetic method is limited to the reaction of phosphorus ylides with carbonyl compounds, see: Brium, G. H.; Matthews, C. N. J. Chem. Soc., Chem. Commun. 1967, 137. Ramirez, F.; Smith, C. P.; Pilot, J. F. J. Am. Chem. Soc. 1968, 90, 6726. Aly, H. A. E.; Barlow, J. H.; Russell, D. R.; Smith, D. J. H.; Swindles, M.; Trippett, S. J. Chem. Soc., Chem. Commun. 1976, 449. Bestmann, H. J.; Roth, K.; Wilheim, E.; Böhme, R.; Burzlaff, H. Angew. Chem., Int. Ed. Engl. 1979, 18, 876. Saalfrank, R. W.; Paul, W.; Liebenow, H. Angew. Chem., Int. Ed. Engl. 1980, 19, 713. Trishin, J. G.; Konovalova, I. V.; Burangulova, R. N.; Burnaeva, L. A.; Chistokletov, V. N.; Pudovik, A. N .Tetrahedron Lett. 1989, 30, 577. Huang, Y.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1991, 113, 7800. Huang, Y.; Sopchik, A. E.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1993, 115, 4031.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 577
    • Trishin, J.G.1    Konovalova, I.V.2    Burangulova, R.N.3    Burnaeva, L.A.4    Chistokletov, V.N.5    Pudovik, A.N.6
  • 27
    • 0001574569 scopus 로고
    • Several isolable pentacoordinate 1,2-oxaphosphetanes have been reported, but their synthetic method is limited to the reaction of phosphorus ylides with carbonyl compounds, see: Brium, G. H.; Matthews, C. N. J. Chem. Soc., Chem. Commun. 1967, 137. Ramirez, F.; Smith, C. P.; Pilot, J. F. J. Am. Chem. Soc. 1968, 90, 6726. Aly, H. A. E.; Barlow, J. H.; Russell, D. R.; Smith, D. J. H.; Swindles, M.; Trippett, S. J. Chem. Soc., Chem. Commun. 1976, 449. Bestmann, H. J.; Roth, K.; Wilheim, E.; Böhme, R.; Burzlaff, H. Angew. Chem., Int. Ed. Engl. 1979, 18, 876. Saalfrank, R. W.; Paul, W.; Liebenow, H. Angew. Chem., Int. Ed. Engl. 1980, 19, 713. Trishin, J. G.; Konovalova, I. V.; Burangulova, R. N.; Burnaeva, L. A.; Chistokletov, V. N.; Pudovik, A. N .Tetrahedron Lett. 1989, 30, 577. Huang, Y.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1991, 113, 7800. Huang, Y.; Sopchik, A. E.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1993, 115, 4031.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 7800
    • Huang, Y.1    Arif, A.M.2    Bentrude, W.G.3
  • 28
    • 0001363091 scopus 로고
    • Several isolable pentacoordinate 1,2-oxaphosphetanes have been reported, but their synthetic method is limited to the reaction of phosphorus ylides with carbonyl compounds, see: Brium, G. H.; Matthews, C. N. J. Chem. Soc., Chem. Commun. 1967, 137. Ramirez, F.; Smith, C. P.; Pilot, J. F. J. Am. Chem. Soc. 1968, 90, 6726. Aly, H. A. E.; Barlow, J. H.; Russell, D. R.; Smith, D. J. H.; Swindles, M.; Trippett, S. J. Chem. Soc., Chem. Commun. 1976, 449. Bestmann, H. J.; Roth, K.; Wilheim, E.; Böhme, R.; Burzlaff, H. Angew. Chem., Int. Ed. Engl. 1979, 18, 876. Saalfrank, R. W.; Paul, W.; Liebenow, H. Angew. Chem., Int. Ed. Engl. 1980, 19, 713. Trishin, J. G.; Konovalova, I. V.; Burangulova, R. N.; Burnaeva, L. A.; Chistokletov, V. N.; Pudovik, A. N .Tetrahedron Lett. 1989, 30, 577. Huang, Y.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1991, 113, 7800. Huang, Y.; Sopchik, A. E.; Arif, A. M.; Bentrude, W. G. J. Am. Chem. Soc. 1993, 115, 4031.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 4031
    • Huang, Y.1    Sopchik, A.E.2    Arif, A.M.3    Bentrude, W.G.4
  • 33
    • 84981772814 scopus 로고
    • Schlosser, M.; Chritmann, K. F. Angew. Chem., Int. Ed. Engl. 1966, 5, 126. Schlosser, M.; Chritmann, K. F. Synthesis 1969, 38. The α-lithiation of an oxaphosphetane was first reported in the following paper: Schlosser, M.; Piskala, A.; Tarchini, C.; Tuong, H. B. Chimia 1975, 29, 341. But, the results could not be reproduced, see: Vedejs, E.; Meier, G. P. Angew. Chem., Int. Ed. Engl. 1983, 22, 56.
    • (1966) Angew. Chem., Int. Ed. Engl. , vol.5 , pp. 126
    • Schlosser, M.1    Chritmann, K.F.2
  • 34
    • 0013150269 scopus 로고
    • Schlosser, M.; Chritmann, K. F. Angew. Chem., Int. Ed. Engl. 1966, 5, 126. Schlosser, M.; Chritmann, K. F. Synthesis 1969, 38. The α-lithiation of an oxaphosphetane was first reported in the following paper: Schlosser, M.; Piskala, A.; Tarchini, C.; Tuong, H. B. Chimia 1975, 29, 341. But, the results could not be reproduced, see: Vedejs, E.; Meier, G. P. Angew. Chem., Int. Ed. Engl. 1983, 22, 56.
    • (1969) Synthesis , pp. 38
    • Schlosser, M.1    Chritmann, K.F.2
  • 35
    • 0001281673 scopus 로고
    • Schlosser, M.; Chritmann, K. F. Angew. Chem., Int. Ed. Engl. 1966, 5, 126. Schlosser, M.; Chritmann, K. F. Synthesis 1969, 38. The α-lithiation of an oxaphosphetane was first reported in the following paper: Schlosser, M.; Piskala, A.; Tarchini, C.; Tuong, H. B. Chimia 1975, 29, 341. But, the results could not be reproduced, see: Vedejs, E.; Meier, G. P. Angew. Chem., Int. Ed. Engl. 1983, 22, 56.
    • (1975) Chimia , vol.29 , pp. 341
    • Schlosser, M.1    Piskala, A.2    Tarchini, C.3    Tuong, H.B.4
  • 36
    • 57549108561 scopus 로고
    • Schlosser, M.; Chritmann, K. F. Angew. Chem., Int. Ed. Engl. 1966, 5, 126. Schlosser, M.; Chritmann, K. F. Synthesis 1969, 38. The α-lithiation of an oxaphosphetane was first reported in the following paper: Schlosser, M.; Piskala, A.; Tarchini, C.; Tuong, H. B. Chimia 1975, 29, 341. But, the results could not be reproduced, see: Vedejs, E.; Meier, G. P. Angew. Chem., Int. Ed. Engl. 1983, 22, 56.
    • (1983) Angew. Chem., Int. Ed. Engl. , vol.22 , pp. 56
    • Vedejs, E.1    Meier, G.P.2
  • 37
    • 0001388593 scopus 로고
    • For 3-vinyl derivatives, see: Ref. 15b
    • 1,2-Oxaphosphetanes having a phenyl or vinyl group at the 3-position, prepared from semi-stabilized phosphorus ylides, were observed: for phenyl derivatives, see: Ward, W. J., Jr.; McEwen, W. E. J. Org. Chem. 1990, 55, 493-500. For 3-vinyl derivatives, see: Ref. 15b.
    • (1990) J. Org. Chem. , vol.55 , pp. 493-500
    • Ward Jr., W.J.1    McEwen, W.E.2
  • 47
    • 33847802643 scopus 로고
    • Hudrlik, P. F.; Peterson, D. J. Am. Chem. Soc. 1975, 97, 1464. Hudrlik, P. F.; Peterson, D.; Rona, R. J. J. Org. Chem. 1975, 40, 2263. Hudrlik, P .F.; Agwaramgbo, E. L. O.; Hudrlik, A. M. J. Org. Chem. 1989, 54, 5613.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 1464
    • Hudrlik, P.F.1    Peterson, D.2
  • 48
    • 33847801712 scopus 로고
    • Hudrlik, P. F.; Peterson, D. J. Am. Chem. Soc. 1975, 97, 1464. Hudrlik, P. F.; Peterson, D.; Rona, R. J. J. Org. Chem. 1975, 40, 2263. Hudrlik, P .F.; Agwaramgbo, E. L. O.; Hudrlik, A. M. J. Org. Chem. 1989, 54, 5613.
    • (1975) J. Org. Chem. , vol.40 , pp. 2263
    • Hudrlik, P.F.1    Peterson, D.2    Rona, R.J.3
  • 49
    • 0024826190 scopus 로고
    • Hudrlik, P. F.; Peterson, D. J. Am. Chem. Soc. 1975, 97, 1464. Hudrlik, P. F.; Peterson, D.; Rona, R. J. J. Org. Chem. 1975, 40, 2263. Hudrlik, P .F.; Agwaramgbo, E. L. O.; Hudrlik, A. M. J. Org. Chem. 1989, 54, 5613.
    • (1989) J. Org. Chem. , vol.54 , pp. 5613
    • Hudrlik, P.F.1    Agwaramgbo, E.L.O.2    Hudrlik, A.M.3
  • 59
    • 0027179719 scopus 로고
    • Pelter, A.; Buss, D.; Colclough, E.; Singaram, B. Tetrahedron 1993, 49, 7077. Pelter, A.; Singaram, B.; Wilson, J. W. Tetrahedron Lett. 1983, 24, 635. Pelter, A.; Singaram, B.; Williams, L.; Wilson, J. W. Tetrahedron, 1993, 49, 2965.
    • (1993) Tetrahedron , vol.49 , pp. 7077
    • Pelter, A.1    Buss, D.2    Colclough, E.3    Singaram, B.4
  • 60
    • 0342416061 scopus 로고
    • Pelter, A.; Buss, D.; Colclough, E.; Singaram, B. Tetrahedron 1993, 49, 7077. Pelter, A.; Singaram, B.; Wilson, J. W. Tetrahedron Lett. 1983, 24, 635. Pelter, A.; Singaram, B.; Williams, L.; Wilson, J. W. Tetrahedron, 1993, 49, 2965.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 635
    • Pelter, A.1    Singaram, B.2    Wilson, J.W.3
  • 61
    • 0027479921 scopus 로고
    • Pelter, A.; Buss, D.; Colclough, E.; Singaram, B. Tetrahedron 1993, 49, 7077. Pelter, A.; Singaram, B.; Wilson, J. W. Tetrahedron Lett. 1983, 24, 635. Pelter, A.; Singaram, B.; Williams, L.; Wilson, J. W. Tetrahedron, 1993, 49, 2965.
    • (1993) Tetrahedron , vol.49 , pp. 2965
    • Pelter, A.1    Singaram, B.2    Williams, L.3    Wilson, J.W.4


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