메뉴 건너뛰기




Volumn 60, Issue 21, 1995, Pages 6706-6716

Ring Closure Reactions of Substituted 4-Pentenyl-l-oxy Radicals. The Stereoselective Synthesis of Functionalized Disubstituted Tetrahydrofurans

Author keywords

[No Author keywords available]

Indexed keywords

TETRAHYDROFURAN DERIVATIVE;

EID: 0028826606     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo00126a021     Document Type: Article
Times cited : (105)

References (62)
  • 10
    • 0000012312 scopus 로고
    • Morrison, J. D., Ed.; Academic Press: New York
    • Bartlett, P. A. In Asymmetric Synthesis; Morrison, J. D., Ed.; Academic Press: New York, 1984; Vol. 3, pp 411-453.
    • (1984) Asymmetric Synthesis , vol.3 , pp. 411-453
    • Bartlett, P.A.1
  • 38
    • 85022371389 scopus 로고
    • Chem. Abstr. 1988, 108, 94312b.
    • (1988) Chem. Abstr. , vol.108 , pp. 94312b
  • 44
    • 84918198334 scopus 로고
    • Chem. Abstr. 1964, 60, 4094b.
    • (1964) Chem. Abstr. , vol.60 , pp. 4094b
  • 46
    • 85022386109 scopus 로고
    • 2 = 0.999). The reverse reaction 8 — 6 was ruled out by reducing 2-(bromomethyl)tetrahydrofuran and 2-(bromomethyl)-5-tert-butyltet-rahydrofuran (transxis = 63:37)
    • 2 = 0.999). The reverse reaction 8 — 6 was ruled out by reducing 2-(bromomethyl)tetrahydrofuran (Bresson, A.; Dauphin, G.; Geneste, J.-M.; Kergomard, A.; Lacourt, A. Bull. Soc. Chim. Fr. 1973, 1080) and 2-(bromomethyl)-5-tert-butyltet-rahydrofuran (transxis = 63:37)
    • (1973) Bull. Soc. Chim. Fr. , pp. 1080
    • Bresson, A.1    Dauphin, G.2    Geneste, J.-M.3    Kergomard, A.4    Lacourt, A.5
  • 47
    • 85022412219 scopus 로고
    • 3SnH at T = 80 °C. Both transformations afford the cyclic products (2-methyltetrahydrofuran (10a): 62%, 2-teri-butyl-5-methyltetrahydrofuran (transxis = 65:35) (10m): 90%) without traces of alkenols la or lm
    • 3SnH at T = 80 °C. Both transformations afford the cyclic products (2-methyltetrahydrofuran (10a): 62%, 2-teri-butyl-5-methyltetrahydrofuran (transxis = 65:35) (10m): 90%) without traces of alkenols la or lm.
    • (1947) Bull. Soc. Chim. Fr. , pp. 15
    • Colonge, J.1    Lagier, A.2
  • 48
    • 0000020896 scopus 로고
    • For exo.endo selectivity in 5-hexenyl radical cyclizations see
    • For exo.endo selectivity in 5-hexenyl radical cyclizations see: Beckwith, A. L. J.; Schiesser, C. H. Tetrahedron 1985, 41, 3925.
    • (1985) Tetrahedron , vol.41 , pp. 3925
    • Beckwith, A.L.J.1    Schiesser, C.H.2
  • 49
    • 0343321133 scopus 로고
    • 3NS (228.5); MS (EI) m/z (rel intensity) 227, 229, 231, 233 (10, 9, 3, 1), 192,194, 196 (100, 67, 15), 78 (76)
    • 3NS (228.5); MS (EI) m/z (rel intensity) 227, 229, 231, 233 (10, 9, 3, 1), 192,194, 196 (100, 67, 15), 78 (76). Barton, D. H. R.; Lacher, B.; Zard, S. Z. Tetrahedron Lett. 1985, 26, 5939.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 5939
    • Barton, D.H.R.1    Lacher, B.2    Zard, S.Z.3
  • 50
    • 0037862197 scopus 로고
    • This estimation was calculated using the following bond energies: C-C 370 kJ/mol, C=C 685 kJ/mol, C-0 382 kJ/mol
    • This estimation was calculated using the following bond energies: C-C 370 kJ/mol, C=C 685 kJ/mol, C-0 382 kJ/mol: Kerr, J. A. Chem. Rev. 1966, 66, 465.
    • (1966) Chem. Rev. , vol.66 , pp. 465
    • Kerr, J.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.