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Volumn 43, Issue 37, 2002, Pages 6511-6514

Synthesis of carbo- and aza-bicyclo[4.3.0] and [4.4.0] compounds by Ti(II)-mediated cyclization of 2,7- or 2,8-enynyl-1-ol derivatives

Author keywords

Bicyclo 4.3.0 ; Bicyclo 4.4.0 ; Ti(II) mediated cyclization

Indexed keywords

2,7 ENYNYL 1 OL; 2,8 ENYNYL 1 OL; ALCOHOL DERIVATIVE; METAL COMPLEX; REAGENT; TITANIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037048496     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01474-0     Document Type: Article
Times cited : (8)

References (19)
  • 11
    • 0038455271 scopus 로고    scopus 로고
    • Marek, I., Ed.; Wiley-VCH; Chapter 9
    • 4/2 i-PrMgX reagent: (a) Sato, F.; Urabe, H. In Titanium and Zirconium in Organic Synthesis; Marek, I., Ed.; Wiley-VCH, 2002; Chapter 9; (b) Sato, F.; Okamoto, S. Adv. Synth. Catal. 2001, 343, 759; (c) Sato, F.; Urabe, H.; Okamoto, S. Chem. Rev. 2000, 100, 2835.
    • (2002) Titanium and Zirconium in Organic Synthesis
    • Sato, F.1    Urabe, H.2
  • 12
    • 0000332902 scopus 로고    scopus 로고
    • 4/2 i-PrMgX reagent: (a) Sato, F.; Urabe, H. In Titanium and Zirconium in Organic Synthesis; Marek, I., Ed.; Wiley-VCH, 2002; Chapter 9; (b) Sato, F.; Okamoto, S. Adv. Synth. Catal. 2001, 343, 759; (c) Sato, F.; Urabe, H.; Okamoto, S. Chem. Rev. 2000, 100, 2835.
    • (2001) Adv. Synth. Catal. , vol.343 , pp. 759
    • Sato, F.1    Okamoto, S.2
  • 13
    • 0034249727 scopus 로고    scopus 로고
    • 4/2 i-PrMgX reagent: (a) Sato, F.; Urabe, H. In Titanium and Zirconium in Organic Synthesis; Marek, I., Ed.; Wiley-VCH, 2002; Chapter 9; (b) Sato, F.; Okamoto, S. Adv. Synth. Catal. 2001, 343, 759; (c) Sato, F.; Urabe, H.; Okamoto, S. Chem. Rev. 2000, 100, 2835.
    • (2000) Chem. Rev. , vol.100 , pp. 2835
    • Sato, F.1    Urabe, H.2    Okamoto, S.3
  • 16
    • 0011163622 scopus 로고    scopus 로고
    • 1H NMR analysis and was postulated to be (E)-configuration based on the mechanistic viewpoint.
    • 1H NMR analysis and was postulated to be (E)-configuration based on the mechanistic viewpoint.
  • 19
    • 9344230921 scopus 로고
    • The configuration of the major product trans-12 was confirmed by derivatization to the authentic trans-1,1-di(hydroxymethyl)octahydronaphthalene 19, which was prepared by reduction of the known compound trans-20 [Oppolzer, W.; Gaudin, J.-M.; Birkinshaw, T. N. Tetrahedron Lett. 1988, 29, 4705].
    • (1988) Tetrahedron Lett. , vol.29 , pp. 4705
    • Oppolzer, W.1    Gaudin, J.-M.2    Birkinshaw, T.N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.