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Volumn 4, Issue 8, 2009, Pages 1113-1117

Synthesis of bicyclo[5.3.0]azulene derivatives

Author keywords

[No Author keywords available]

Indexed keywords

2,2 DIMETHOXYPROPANE; 7 OXOCYCLOHEPTA 1,3,5 TRIENYL 4 METHYLBENZENESULFONATE; AZULENE DERIVATIVE; LACTONE; METHYL 2 METHYLAZULENE 1 CARBOXYLATE; METHYL 2 OXO 2H CYCLOHEPTA[B]FURAN 3 CARBOXYLATE; PROPANE; TROPOLONE; UNCLASSIFIED DRUG; VINYL DERIVATIVE; VINYL ETHER;

EID: 68449096141     PISSN: 17542189     EISSN: 17502799     Source Type: Journal    
DOI: 10.1038/nprot.2009.99     Document Type: Article
Times cited : (7)

References (20)
  • 1
    • 0344550361 scopus 로고    scopus 로고
    • Tuning the color and excited state properties of the azulenic chromophore: NIR absorbing pigments and materials
    • Liu, R.S.H. & Asato, A.E. Tuning the color and excited state properties of the azulenic chromophore: NIR absorbing pigments and materials. J. Photochem. Photobiol. C, Photochem. Rev. 4, 179-194 (2003).
    • (2003) J. Photochem. Photobiol. C, Photochem. Rev , vol.4 , pp. 179-194
    • Liu, R.S.H.1    Asato, A.E.2
  • 2
    • 0035318612 scopus 로고    scopus 로고
    • A clearer vision for in vivo imaging
    • Weissleder, R. A clearer vision for in vivo imaging. Nat. Biotechnol. 19, 316-317 (2001).
    • (2001) Nat. Biotechnol , vol.19 , pp. 316-317
    • Weissleder, R.1
  • 3
    • 0035111619 scopus 로고    scopus 로고
    • HNS-32, a novel azulene-1-carboxamidine derivative, inhibits nifedipine-sensitive and -insensitive contraction of the isolated rabbit aorta
    • Tanaka, Y. et al. HNS-32, a novel azulene-1-carboxamidine derivative, inhibits nifedipine-sensitive and -insensitive contraction of the isolated rabbit aorta. Naunyn Schmiedebergs Arch. Pharmacol. 363, 344-352 (2001).
    • (2001) Naunyn Schmiedebergs Arch. Pharmacol , vol.363 , pp. 344-352
    • Tanaka, Y.1
  • 5
    • 0001468428 scopus 로고
    • Non-benzenoid aromatic compounds and the concept of aromaticity
    • Volpin, M.E. Non-benzenoid aromatic compounds and the concept of aromaticity. Russ. Chem. Rev. 29, 129-160 (1960).
    • (1960) Russ. Chem. Rev , vol.29 , pp. 129-160
    • Volpin, M.E.1
  • 6
    • 2842587859 scopus 로고
    • The synthesis of azulene-1-alkeanoic acids, azulene-1,3-dialkanoic acids, and related compounds. A 1,3-bridge azulene
    • Anderson, A.G. & Breazeale, R.D. The synthesis of azulene-1-alkeanoic acids, azulene-1,3-dialkanoic acids, and related compounds. A 1,3-bridge azulene. J. Org. Chem. 34, 2375-2384 (1969).
    • (1969) J. Org. Chem , vol.34 , pp. 2375-2384
    • Anderson, A.G.1    Breazeale, R.D.2
  • 7
    • 0034114573 scopus 로고    scopus 로고
    • Synthesis of beta-(1-azulenyl)-L-alanine as a potential blue-colored fluorescent tryptophan analog and its use in peptide synthesis
    • Loidl, G. et al. Synthesis of beta-(1-azulenyl)-L-alanine as a potential blue-colored fluorescent tryptophan analog and its use in peptide synthesis. J. Pept. Sci. 6, 139-144 (2000).
    • (2000) J. Pept. Sci , vol.6 , pp. 139-144
    • Loidl, G.1
  • 8
    • 0032751522 scopus 로고    scopus 로고
    • Decarbonylation reaction of 1-azulenecarbaldehydes under mild conditions. A strategy for the protection of 1- and/or 3-position of azulene rings
    • Ito, S., Morita, N. & Asao, T. Decarbonylation reaction of 1-azulenecarbaldehydes under mild conditions. A strategy for the protection of 1- and/or 3-position of azulene rings. Bull. Chem. Soc. Jpn. 72, 2543-2548 (1999).
    • (1999) Bull. Chem. Soc. Jpn , vol.72 , pp. 2543-2548
    • Ito, S.1    Morita, N.2    Asao, T.3
  • 9
    • 84987493170 scopus 로고
    • Thermal reaction of azulene and some of its symmetrically substituted methyl derivatives with dimethyl acetylenedicarboxylate
    • Chen, Y. & Hansen, H.J. Thermal reaction of azulene and some of its symmetrically substituted methyl derivatives with dimethyl acetylenedicarboxylate. Helv. Chim. Acta 76, 168-177 (1993).
    • (1993) Helv. Chim. Acta , vol.76 , pp. 168-177
    • Chen, Y.1    Hansen, H.J.2
  • 10
    • 34250380430 scopus 로고    scopus 로고
    • The novel transition metal free synthesis of 1,1′-biazulene
    • Shoji, T., Ito, S., Toyota, K., Yasunami, M. & Morita, N. The novel transition metal free synthesis of 1,1′-biazulene. Tetrahedron Lett. 48, 4999-5002 (2007).
    • (2007) Tetrahedron Lett , vol.48 , pp. 4999-5002
    • Shoji, T.1    Ito, S.2    Toyota, K.3    Yasunami, M.4    Morita, N.5
  • 11
    • 0043037545 scopus 로고
    • Nucleophilic reaction of azulene derivatives with some ketone enolates
    • Fukazawa, Y., Usui, S., Kurata, Y., Takeda, Y. & Saito, N. Nucleophilic reaction of azulene derivatives with some ketone enolates. J. Org. Chem. 54, 2982-2985 (1988).
    • (1988) J. Org. Chem , vol.54 , pp. 2982-2985
    • Fukazawa, Y.1    Usui, S.2    Kurata, Y.3    Takeda, Y.4    Saito, N.5
  • 12
    • 84988073258 scopus 로고
    • Vicarious nucleophilic substitution (VNS) of hydrogen in azulenes
    • Makosza, M., Kuciak, R. & Wojciechowski, K. Vicarious nucleophilic substitution (VNS) of hydrogen in azulenes. Liebigs Ann. Chem. 1994, 615-618 (1994).
    • (1994) Liebigs Ann. Chem , vol.1994 , pp. 615-618
    • Makosza, M.1    Kuciak, R.2    Wojciechowski, K.3
  • 15
    • 0342781937 scopus 로고
    • Elektronenreiche heptafulvene als bausteine von azulenen. 8-methoxyheptafulven.
    • Hasenhundl, A., Rapp, K.M. & Daub, J. Elektronenreiche heptafulvene als bausteine von azulenen. 8-methoxyheptafulven. Chem. Lett. 8, 597-600 (1979).
    • (1979) Chem. Lett , vol.8 , pp. 597-600
    • Hasenhundl, A.1    Rapp, K.M.2    Daub, J.3
  • 16
    • 0001073696 scopus 로고
    • Heptafulvene (methylenecycloheptatriene)
    • von Doering, W. & Wiley, D.W. Heptafulvene (methylenecycloheptatriene). Tetrahedron 11, 183-198 (1960).
    • (1960) Tetrahedron , vol.11 , pp. 183-198
    • von Doering, W.1    Wiley, D.W.2
  • 17
    • 39749138671 scopus 로고    scopus 로고
    • Synthesis of methyl 2-methylazulene-3-carboxylate in the presence of molecular sieves and reaction with N-bromosuccinimide
    • Wang, D.L., Xu, J., Gu, Z., Han, S. & Imafuku, K. Synthesis of methyl 2-methylazulene-3-carboxylate in the presence of molecular sieves and reaction with N-bromosuccinimide. Synth. Commun. 38, 991-996 (2008).
    • (2008) Synth. Commun , vol.38 , pp. 991-996
    • Wang, D.L.1    Xu, J.2    Gu, Z.3    Han, S.4    Imafuku, K.5
  • 18
    • 0036134104 scopus 로고    scopus 로고
    • Pham, W., Weissleder, R. & Tung, C.-H. Intermolecular[8+2] cycloaddition reactions of 2H-3-methoxycarbonylcyclohepta[b]furan-2-one with vinyl ethers: An approach to bicyclo[5.3.0]azulene derivatives. Tetrahedron Lett. 43, 19-20 (2001).
    • Pham, W., Weissleder, R. & Tung, C.-H. Intermolecular[8+2] cycloaddition reactions of 2H-3-methoxycarbonylcyclohepta[b]furan-2-one with vinyl ethers: An approach to bicyclo[5.3.0]azulene derivatives. Tetrahedron Lett. 43, 19-20 (2001).
  • 19
    • 0037433799 scopus 로고    scopus 로고
    • A practical approach for the preparation of monofunctional azulenyl squaraine dye
    • Pham, W., Weissleder, R. & Tung, C.-H. A practical approach for the preparation of monofunctional azulenyl squaraine dye. Tetrahedron Lett. 44, 3975-3978 (2003).
    • (2003) Tetrahedron Lett , vol.44 , pp. 3975-3978
    • Pham, W.1    Weissleder, R.2    Tung, C.-H.3
  • 20
    • 39749162789 scopus 로고    scopus 로고
    • 8+2] Cycloaddition reactions in organic synthesis
    • Nair, V. & Abhilash, K.G. [8+2] Cycloaddition reactions in organic synthesis. Synlett 3, 301-312 (2008).
    • (2008) Synlett , vol.3 , pp. 301-312
    • Nair, V.1    Abhilash, K.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.