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Volumn 62, Issue 16, 1997, Pages 5575-5577

Synthesis and Applications of Tetrahydrofuran-Stable Substituted (3-Lithioxyalkyl)- and (4-Lithioxyalkyl)lithiums, Modified with Magnesium 2-Ethoxyethoxide

Author keywords

[No Author keywords available]

Indexed keywords

BENZOPHENONE; KETONE; LITHIUM DERIVATIVE; ORGANOLITHIUM COMPOUND; TETRAHYDROFURAN;

EID: 0030878644     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9703010     Document Type: Article
Times cited : (22)

References (47)
  • 1
    • 0000897606 scopus 로고
    • For selected reviews, see: (a) Stowell, J. C. Chem. Rev. 1984, 84, 409. (b) Klumpp, G. W. Recl. Trav. Chim. Pays-Bas 1986, 105, 1. (c) Yus, M. Chem. Soc. Rev. 1996, 155.
    • (1984) Chem. Rev. , vol.84 , pp. 409
    • Stowell, J.C.1
  • 2
    • 84987082416 scopus 로고
    • For selected reviews, see: (a) Stowell, J. C. Chem. Rev. 1984, 84, 409. (b) Klumpp, G. W. Recl. Trav. Chim. Pays-Bas 1986, 105, 1. (c) Yus, M. Chem. Soc. Rev. 1996, 155.
    • (1986) Recl. Trav. Chim. Pays-Bas , vol.105 , pp. 1
    • Klumpp, G.W.1
  • 3
    • 0030496093 scopus 로고    scopus 로고
    • For selected reviews, see: (a) Stowell, J. C. Chem. Rev. 1984, 84, 409. (b) Klumpp, G. W. Recl. Trav. Chim. Pays-Bas 1986, 105, 1. (c) Yus, M. Chem. Soc. Rev. 1996, 155.
    • (1996) Chem. Soc. Rev. , pp. 155
    • Yus, M.1
  • 16
    • 0003491250 scopus 로고
    • Barton, D., Ollis, W. D., Eds.; Pergamon Press: Oxford, pp 943ff
    • Wakefield, B. J. In Comprehensive Organic Chemistry; Barton, D., Ollis, W. D., Eds.; Pergamon Press: Oxford, 1979, Vol. 3, pp 943ff.
    • (1979) Comprehensive Organic Chemistry , vol.3
    • Wakefield, B.J.1
  • 19
    • 0008332125 scopus 로고
    • For selected examples of similar methods for synthesis of allylic or homoallylic alcohols, see: (a) Marcou, A.; Normant, H. Bull. Soc. Chim. Fr. 1965, 12, 3491. (b) Katzenellenbogen, J. A.; Lenox, R. S. J. Org. Chem. 1973, 38, 326. (c) Masamune, T.; Sato, S.; Abiko, A.; Ono, M.; Murai, A. Bull. Chem. Soc. Jpn 1980, 53, 2895. (d) Oppolzer, W.; Schneider, P. Tetrahedron Lett. 1984, 25, 3305.
    • (1965) Bull. Soc. Chim. Fr. , vol.12 , pp. 3491
    • Marcou, A.1    Normant, H.2
  • 20
    • 0001111467 scopus 로고
    • For selected examples of similar methods for synthesis of allylic or homoallylic alcohols, see: (a) Marcou, A.; Normant, H. Bull. Soc. Chim. Fr. 1965, 12, 3491. (b) Katzenellenbogen, J. A.; Lenox, R. S. J. Org. Chem. 1973, 38, 326. (c) Masamune, T.; Sato, S.; Abiko, A.; Ono, M.; Murai, A. Bull. Chem. Soc. Jpn 1980, 53, 2895. (d) Oppolzer, W.; Schneider, P. Tetrahedron Lett. 1984, 25, 3305.
    • (1973) J. Org. Chem. , vol.38 , pp. 326
    • Katzenellenbogen, J.A.1    Lenox, R.S.2
  • 21
    • 0008226958 scopus 로고
    • For selected examples of similar methods for synthesis of allylic or homoallylic alcohols, see: (a) Marcou, A.; Normant, H. Bull. Soc. Chim. Fr. 1965, 12, 3491. (b) Katzenellenbogen, J. A.; Lenox, R. S. J. Org. Chem. 1973, 38, 326. (c) Masamune, T.; Sato, S.; Abiko, A.; Ono, M.; Murai, A. Bull. Chem. Soc. Jpn 1980, 53, 2895. (d) Oppolzer, W.; Schneider, P. Tetrahedron Lett. 1984, 25, 3305.
    • (1980) Bull. Chem. Soc. Jpn , vol.53 , pp. 2895
    • Masamune, T.1    Sato, S.2    Abiko, A.3    Ono, M.4    Murai, A.5
  • 22
    • 0001095242 scopus 로고
    • For selected examples of similar methods for synthesis of allylic or homoallylic alcohols, see: (a) Marcou, A.; Normant, H. Bull. Soc. Chim. Fr. 1965, 12, 3491. (b) Katzenellenbogen, J. A.; Lenox, R. S. J. Org. Chem. 1973, 38, 326. (c) Masamune, T.; Sato, S.; Abiko, A.; Ono, M.; Murai, A. Bull. Chem. Soc. Jpn 1980, 53, 2895. (d) Oppolzer, W.; Schneider, P. Tetrahedron Lett. 1984, 25, 3305.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 3305
    • Oppolzer, W.1    Schneider, P.2
  • 23
    • 85033151253 scopus 로고    scopus 로고
    • The use of other (3-lithioxypropyl)lithiums in a γ-butyrolactone synthesis has been reported; see refs 2, 3a, and 6
    • The use of other (3-lithioxypropyl)lithiums in a γ-butyrolactone synthesis has been reported; see refs 2, 3a, and 6.
  • 24
    • 33947085593 scopus 로고
    • For selected examples of syntheses of γ- and δ-lactones, see: (a) Trost, B. M.; Bogdanowicz, M. J. J. Am. Chem. Soc. 1973, 95, 5321. (b) Canonne, P.; Foscolos, G. B.; Bélanger, D. J. Org. Chem. 1980, 45, 1828. (c) Canonne, P.; Bélanger, D.; Lemay, G.; Foscolos, G. B. J. Org. Chem. 1981, 46, 3091. (d) Schlecht, M. F.; Kim, H.-J. Tetrahedron Lett. 1985, 26, 127.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 5321
    • Trost, B.M.1    Bogdanowicz, M.J.2
  • 25
    • 0001052025 scopus 로고
    • For selected examples of syntheses of γ- and δ-lactones, see: (a) Trost, B. M.; Bogdanowicz, M. J. J. Am. Chem. Soc. 1973, 95, 5321. (b) Canonne, P.; Foscolos, G. B.; Bélanger, D. J. Org. Chem. 1980, 45, 1828. (c) Canonne, P.; Bélanger, D.; Lemay, G.; Foscolos, G. B. J. Org. Chem. 1981, 46, 3091. (d) Schlecht, M. F.; Kim, H.-J. Tetrahedron Lett. 1985, 26, 127.
    • (1980) J. Org. Chem. , vol.45 , pp. 1828
    • Canonne, P.1    Foscolos, G.B.2    Bélanger, D.3
  • 26
    • 0001238632 scopus 로고
    • For selected examples of syntheses of γ- and δ-lactones, see: (a) Trost, B. M.; Bogdanowicz, M. J. J. Am. Chem. Soc. 1973, 95, 5321. (b) Canonne, P.; Foscolos, G. B.; Bélanger, D. J. Org. Chem. 1980, 45, 1828. (c) Canonne, P.; Bélanger, D.; Lemay, G.; Foscolos, G. B. J. Org. Chem. 1981, 46, 3091. (d) Schlecht, M. F.; Kim, H.-J. Tetrahedron Lett. 1985, 26, 127.
    • (1981) J. Org. Chem. , vol.46 , pp. 3091
    • Canonne, P.1    Bélanger, D.2    Lemay, G.3    Foscolos, G.B.4
  • 27
    • 0002674996 scopus 로고
    • For selected examples of syntheses of γ- and δ-lactones, see: (a) Trost, B. M.; Bogdanowicz, M. J. J. Am. Chem. Soc. 1973, 95, 5321. (b) Canonne, P.; Foscolos, G. B.; Bélanger, D. J. Org. Chem. 1980, 45, 1828. (c) Canonne, P.; Bélanger, D.; Lemay, G.; Foscolos, G. B. J. Org. Chem. 1981, 46, 3091. (d) Schlecht, M. F.; Kim, H.-J. Tetrahedron Lett. 1985, 26, 127.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 127
    • Schlecht, M.F.1    Kim, H.-J.2
  • 29
    • 0000413286 scopus 로고
    • Chairman and Deputy Chairman of the Editorial Board Sir Derek Barton, F.R.S. and W. David Ollis, F.R.S.; Pergamon Press: London
    • (a) Comprehensive Organic Chemistry. The Synthesis and Reactions of Organic Compounds; Chairman and Deputy Chairman of the Editorial Board Sir Derek Barton, F.R.S. and W. David Ollis, F.R.S.; Sutherland, I. O., Ed.; Pergamon Press: London, 1979; Vol 2, pp 869-956.
    • (1979) Comprehensive Organic Chemistry. The Synthesis and Reactions of Organic Compounds , vol.2 , pp. 869-956
    • Sutherland, I.O.1
  • 32
    • 0001210283 scopus 로고
    • (a) Engel, K. H.; Ramming, D. W.; Flath, R. A.; Teranishi, R. J. Agric. Food Chem. 1988, 36, 1003; Chem Abstr. 1988, 109, 127496r.
    • (1988) Chem Abstr. , vol.109
  • 34
    • 0347787756 scopus 로고
    • (b) MacLeod, A. J.; MacLeod, G.; Snyder, C. H. Phytochemistry 1988, 27, 2189; Chem. Abstr. 1988, 109, 148205k.
    • (1988) Chem. Abstr. , vol.109
  • 36
    • 33846000941 scopus 로고
    • (c) Guichard, E.; Souty, M. Z. Lebensm-Unters. Forsch. 1988, 186, 301; Chem Abstr. 1988, 109, 109117p.
    • (1988) Chem Abstr. , vol.109
  • 38
    • 85033140672 scopus 로고
    • (d) Schreier, P.; Drawert, F. Chem., Mikrobiol., Technd. Technol. Lebensm. 1981, 7, 23; Chem. Abstr. 1981, 95, 59882d.
    • (1981) Chem. Abstr. , vol.95
  • 41
    • 0001236184 scopus 로고
    • (f) Georgilopoulos, D. N.; Gallois, A. N. Z. Lebensm-Unters. Forsch. 1987, 184, 374; Chem. Abstr. 1987, 107, 114480q.
    • (1987) Chem. Abstr. , vol.107
  • 43
    • 0011947157 scopus 로고
    • (g) MacLeod, G.; Ames, J. M. Phytochemistry 1990, 29, 165; Chem. Abstr. 1990, 112, 137790h.
    • (1990) Chem. Abstr. , vol.112


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.