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Volumn 36, Issue 5, 2006, Pages 559-571

2-Hydroxy-1,2,3,6-tetrahydro-azulen-6-carboxylic acid ethyl ester - A novel precursor for a new class of liquid crystalline materials

Author keywords

Birch reduction; Carbene addition; Liquid crystals; Ring enlargement

Indexed keywords

2 BROMO 1,2,3,6 TETRAHYDROAZULEN 6 CARBOXYLIC ACID ETHYL ESTER; 2 CHLORO 1,2,3,6 TETRAHYDROAZULEN 6 CARBOXYLIC ACID ETHYL ESTER; 2 HYDROXY 1,2,3,6 TETRAHYDROAZULEN 6 CARBOXYLIC ACID ETHYL ESTER; 2 IODO 1,2,3,6 TETRAHYDROAZULEN 6 CARBOXYLIC ACID ETHYL ESTER; 4 (TERT BUTYLDIPHENYLSILANYLOXY) 1,1A,2,3,4,5,6,6A OCTAHYDROCYCLOPROP[F] INDENE 1 CARBOXYLIC ACID ETHYL ESTER; AZULENE DERIVATIVE; CARBENE; CARBOXYLIC ACID DERIVATIVE; ESTER DERIVATIVE; ETHYL 1,3 DIBROMO 6 AZULEN CARBOXYLATE; ETHYL 2 (TERT BUTYLDIPHENYLSILANYLOXY) 1,2,3,6 TETRAHYDRO 6 AZULEN CARBOXYLATE; HALIDE; UNCLASSIFIED DRUG;

EID: 32644465600     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910500406393     Document Type: Article
Times cited : (4)

References (18)
  • 1
    • 0034833716 scopus 로고    scopus 로고
    • Nematic liquid crystals with a tetrafluoroethylene bridge in the mesogenic core structure
    • Kirsch, P.; Bremer, M.; Huber, F.; Lannert, H.; Ruhl, A.; Lieb, M.; Wallmichrath, T. Nematic liquid crystals with a tetrafluoroethylene bridge in the mesogenic core structure. J. Am. Chem. Soc. 2001, 123, 5414-5417.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 5414-5417
    • Kirsch, P.1    Bremer, M.2    Huber, F.3    Lannert, H.4    Ruhl, A.5    Lieb, M.6    Wallmichrath, T.7
  • 3
    • 0030658383 scopus 로고    scopus 로고
    • Recent liquid crystal material development for active matrix displays
    • (b) Tarumi, K.; Bremer, M.; Geelhaar, T. Recent liquid crystal material development for active matrix displays. Annu. Rev. Mater. Sci. 1997, 27, 423-441.
    • (1997) Annu. Rev. Mater. Sci. , vol.27 , pp. 423-441
    • Tarumi, K.1    Bremer, M.2    Geelhaar, T.3
  • 5
    • 32644484687 scopus 로고
    • Direct replacement of primary hydroxyl groups by halogen
    • Hanessian, S.; Lavallee, P. Direct replacement of primary hydroxyl groups by halogen. Methods Carbohydr. Chem. 1976, 7, 49-55.
    • (1976) Methods Carbohydr. Chem. , vol.7 , pp. 49-55
    • Hanessian, S.1    Lavallee, P.2
  • 9
    • 18544389704 scopus 로고    scopus 로고
    • Ethyl 1, 3-dibromoazulene-6-carboxylate
    • Hussain, Z.; Oeser, T.; Hopf, H. Ethyl 1, 3-dibromoazulene-6-carboxylate. Acta Cryst. 2005, E61, o478-o479.
    • (2005) Acta Cryst. , vol.E61
    • Hussain, Z.1    Oeser, T.2    Hopf, H.3
  • 10
    • 0031352974 scopus 로고    scopus 로고
    • 1-Cyano-2-p-bromophenylazulene and 2-azulenylmethyl 2-anthraquinoate
    • Kaftory, M.; Botoshsnsky, M.; Daub, J.; Mirlach, A. 1-Cyano-2-p- bromophenylazulene and 2-azulenylmethyl 2-anthraquinoate. Acta Cryst. 1997, C53, 1907-1909.
    • (1997) Acta Cryst. , vol.C53 , pp. 1907-1909
    • Kaftory, M.1    Botoshsnsky, M.2    Daub, J.3    Mirlach, A.4
  • 11
    • 0000801279 scopus 로고
    • The triisopropylsilyl group as a hydroxyl-protecting function
    • Cunico, R. F.; Bedell, L. The triisopropylsilyl group as a hydroxyl-protecting function. J. Org. Chem. 1980, 45, 4797-4798.
    • (1980) J. Org. Chem. , vol.45 , pp. 4797-4798
    • Cunico, R.F.1    Bedell, L.2
  • 12
    • 0001920249 scopus 로고
    • Stereocontrolled preparation of 3-acyltetrahydrofurans from acid-promoted rearrangements of allylic ketals: (2S,3S)-3-Acetyl-8-carboethoxy-2,3-dimethyl- 1-oxa-8-azaspiro[4.5]decane
    • Overman, L. E.; Rishton, G. M. Stereocontrolled preparation of 3-acyltetrahydrofurans from acid-promoted rearrangements of allylic ketals: (2S,3S)-3-Acetyl-8-carboethoxy-2,3-dimethyl-1-oxa-8-azaspiro[4.5]decane. Org. Synth. 1992, 71, 63-71;
    • (1992) Org. Synth. , vol.71 , pp. 63-71
    • Overman, L.E.1    Rishton, G.M.2
  • 14
    • 0001356346 scopus 로고
    • L New developments in palladium-catalyzed cross coupling: The coupling of alkyl iodides with alkyl Grignard reagents
    • Widdowson, D. A.; Castle, P. L New developments in palladium-catalyzed cross coupling: The coupling of alkyl iodides with alkyl Grignard reagents. Tetrahedron Lett. 1986, 27, 6013-6016.
    • (1986) Tetrahedron Lett. , vol.27 , pp. 6013-6016
    • Widdowson, D.A.1    Castle, P.2
  • 15
    • 0041771527 scopus 로고
    • Organophosphorus chemistry I. Conversion of alcohol and phenols to halides by tertiary phosphine dihalides
    • (a) Wiley, G. A.; Hershkowitz, R. L.; Rein, B. M.; Chung, B. C. Organophosphorus chemistry I. Conversion of alcohol and phenols to halides by tertiary phosphine dihalides. J. Am. Chem. Soc. 1964, 86, 964-965;
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 964-965
    • Wiley, G.A.1    Hershkowitz, R.L.2    Rein, B.M.3    Chung, B.C.4
  • 16
    • 0000354855 scopus 로고
    • Sugar esters III. New reagent for deoxyhalo sugar preparation
    • (b) Lee, J. B.; Nolan, T. Sugar esters III. New reagent for deoxyhalo sugar preparation. J. Can. J. Chem. 1966, 44, 1331-1334.
    • (1966) J. Can. J. Chem. , vol.44 , pp. 1331-1334
    • Lee, J.B.1    Nolan, T.2
  • 17
    • 0001500794 scopus 로고
    • Direct conversion of silyl ethers into alkyl bromides with boron tribromide
    • Kim, S.; Park, J. H. Direct conversion of silyl ethers into alkyl bromides with boron tribromide. J. Org. Chem. 1988, 53, 3111-3113.
    • (1988) J. Org. Chem. , vol.53 , pp. 3111-3113
    • Kim, S.1    Park, J.H.2
  • 18
    • 0343954600 scopus 로고
    • 1, 5-Methanocyclononatetraenyl anion
    • Radlick, P.; Rosen, W. 1, 5-Methanocyclononatetraenyl anion. J. Am. Chem. Soc. 1966, 88, 3461-3462.
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 3461-3462
    • Radlick, P.1    Rosen, W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.