메뉴 건너뛰기




Volumn 5, Issue 2, 2009, Pages 83-89

Synthesis of coenzyme Q10

Author keywords

Coenzyme Q10; Isoprenol; Sodium p toluenesulfinate

Indexed keywords

2,3 DIMETHOXY 5 METHYL 6 PRENYLQUINOL; 2,3 DIMETHOXY 5 METHYLHYDROQUINONE; 2,3,4,5 TETRAMETHOXY 6 (1 4 TOLUENESULPHINYL 2 METHYLBUT 2 ENE 4 YL)TOLUENE; 2,3,4,5 TETRAMETHOXY 6 (1 BROMO 2 METHYLBUT 2 ENE 4 YL)TOLUENE; 2,3,4,5 TETRAMETHOXY 6 (2 METHYLBUT 2 ENE 1 AL 4 YL)TOLUENE; 2,3,4,5 TETRAMETHOXY 6 (2 METHYLBUT 2 ENE 1 OL 4 YL)TOLUENE; 2,3,4,5 TETRAMETHOXY 6 (2 METHYLBUT 2 ENE 4 YL)TOLUENE; 2,3,4,5 TETRAMETHOXY 6 DECAPRENYLTOLUENE; 2,3,4,5 TETRAMETHOXY 6 PRENYLTOLUENE; BROMINE DERIVATIVE; ISOPRENALINE; LEWIS ACID; QUINONE DERIVATIVE; SOLANESYLBROMIDE; UBIDECARENONE; UNCLASSIFIED DRUG;

EID: 70349664294     PISSN: 15536203     EISSN: None     Source Type: Journal    
DOI: 10.3844/ajidsp.2009.83.89     Document Type: Article
Times cited : (14)

References (27)
  • 1
    • 0029042393 scopus 로고
    • Biochemical, physiological and medical aspects of ubiquinone function
    • Ernster, L. and G. Dallner, 1995. Biochemical, physiological and medical aspects of ubiquinone function. Biochim. Biophys. Acta, 1271: 195-204. http://www.ncbi.nlm.nih.gov/pubmed/7599208
    • (1995) Biochim. Biophys. Acta , vol.1271 , pp. 195-204
    • Ernster, L.1    Dallner, G.2
  • 3
    • 0021151294 scopus 로고
    • In vitro study on contribution of oxidative metabolism of isolated rabbit heart mitochondria to myocardial reperfusion injury
    • Otani, H., H. Tanaka, T. Inoue, M. Umemoto, K. Omoto, K. Tanaka, T. Sato, T. Osako, A. Masuda, A. Nonoyama and T. Kagawam, 1984. In vitro study on contribution of oxidative metabolism of isolated rabbit heart mitochondria to myocardial reperfusion injury. Circ. Res., 55: 168-175. http://circres.ahajournals.org/cgi/content/abstract/55/2/168
    • (1984) Circ. Res , vol.55 , pp. 168-175
    • Otani, H.1    Tanaka, H.2    Inoue, T.3    Umemoto, M.4    Omoto, K.5    Tanaka, K.6    Sato, T.7    Osako, T.8    Masuda, A.9    Nonoyama, A.10    Kagawam, T.11
  • 4
    • 0031785608 scopus 로고    scopus 로고
    • 10 in patients with acute myocardial infarction. Cardiovase. Drug Ther., 12: 347-353. DOI: 10.1023/a:1007764616025
    • 10 in patients with acute myocardial infarction. Cardiovase. Drug Ther., 12: 347-353. DOI: 10.1023/a:1007764616025
  • 5
    • 84993707664 scopus 로고    scopus 로고
    • Complimentary and alternative therapies for hypertension. Complementary Health
    • Warner, M.G., 2000. Complimentary and alternative therapies for hypertension. Complementary Health. Pract. Rev., 6: 11-19. http://chp.sagepub.com/cgi/reprint/6/1/11
    • (2000) Pract. Rev , vol.6 , pp. 11-19
    • Warner, M.G.1
  • 6
    • 0026544566 scopus 로고
    • 10 in the cell: Studies with isolated rat and guinea pig hepatocytes treated with a water-soluble adical initiator
    • 10 in the cell: Studies with isolated rat and guinea pig hepatocytes treated with a water-soluble adical initiator. Biochim. Biphys. Acta, 1123: 309-315. http://www.ncbi.nlm.nih.gov/pubmed/1536870
    • (1992) Biochim. Biphys. Acta , vol.1123 , pp. 309-315
    • Matsura, T.1    Yamada, K.2    Kawasaki, T.3
  • 8
    • 70349678373 scopus 로고    scopus 로고
    • Coenzyme Q
    • Dekker, M, Ed, Chapman and Hall/CRC Press/Kluwer, New York, ISBN: 0-8547-5504-4 9, pp
    • Dallner G. and Stocker R., 2005. Coenzyme Q. Encyclopedia of Dietary Supplements, Dekker, M. (Ed.). Chapman and Hall/CRC Press/Kluwer, New York, ISBN: 0-8547-5504-4 9, pp: 819.
    • (2005) Encyclopedia of Dietary Supplements , pp. 819
    • Dallner, G.1    Stocker, R.2
  • 9
    • 27644434984 scopus 로고
    • Synthese von ubichinon(45) and ubichinon (50)
    • DOI: 10.1002/hlca.19590420733
    • Ruegg, R., U. Gloor, R.N. Goel, G. Ryser, O. Wiss and O. Isler, 1959. Synthese von ubichinon(45) and ubichinon (50). Helv. Chim. Acta, 52: 2616. DOI: 10.1002/hlca.19590420733
    • (1959) Helv. Chim. Acta , vol.52 , pp. 2616
    • Ruegg, R.1    Gloor, U.2    Goel, R.N.3    Ryser, G.4    Wiss, O.5    Isler, O.6
  • 10
  • 12
    • 27644470966 scopus 로고
    • Regioselective polyprenyl rearrangement of polyprenyl 2, 3, 4, 5-tetra-subtituted phenyl ethers promoted by boron trifluoride
    • DOI: 10.1246/cl.1982.1131
    • Yoshizawa, T., H. Toyofuku, K. Tachibana and T. Kuroda, 1982. Regioselective polyprenyl rearrangement of polyprenyl 2, 3, 4, 5-tetra-subtituted phenyl ethers promoted by boron trifluoride. Chem. Lett., 11: 1131-1134. DOI: 10.1246/cl.1982.1131
    • (1982) Chem. Lett , vol.11 , pp. 1131-1134
    • Yoshizawa, T.1    Toyofuku, H.2    Tachibana, K.3    Kuroda, T.4
  • 13
    • 0041007653 scopus 로고
    • Novel solvent effect in the practical synthesis of Ubiquinone-10
    • DOI: 10.1246/cl.1988.1597
    • Eto, H. and C. Eguchi, 1988. Novel solvent effect in the practical synthesis of Ubiquinone-10. Chem. Lett., 1597. DOI: 10.1246/cl.1988.1597
    • (1988) Chem. Lett , pp. 1597
    • Eto, H.1    Eguchi, C.2
  • 14
    • 0001946801 scopus 로고
    • Synthesis and spectroscopic characterization of 13C-labelled ubiquinone-0 and ubiquinone-10
    • Van Liemt, W.B.S., W.F. Steggerda, R. Esmeijer and J. Lugtenburg, 1994. Synthesis and spectroscopic characterization of 13C-labelled ubiquinone-0 and ubiquinone-10. Recl. Trav. Chim. Pays-Bas., 113: 153-161. http://www.scopus.com/scopus/record/ display.url?eid=2-s2.0-0001946801&view= basic&origin=inward&txGid=T37lxC8G9sc8FxnM-Q-fBV1%3a2
    • (1994) Recl. Trav. Chim. Pays-Bas , vol.113 , pp. 153-161
    • Van Liemt, W.B.S.1    Steggerda, W.F.2    Esmeijer, R.3    Lugtenburg, J.4
  • 15
    • 0011865228 scopus 로고
    • Synthesis of ubiquinones. 2. An efficient preparation of ubiquinone-10
    • DOI: 10.1021/jo01319a051
    • Terao, S. K. Kato, M. Shiraishi and H. Morimoto, 1979. Synthesis of ubiquinones. 2. An efficient preparation of ubiquinone-10. J. Org. Chem., 44: 868. DOI: 10.1021/jo01319a051
    • (1979) J. Org. Chem , vol.44 , pp. 868
    • Terao, S.1    Kato, K.2    Shiraishi, M.3    Morimoto, H.4
  • 16
    • 0019989631 scopus 로고
    • A new efficient and stereoselective synthesis of Ubiquinone-10
    • DOI: 10.1246/bcsj.55.1325
    • Fujita, Y., M. Ishiguro, T. Onishi and T. Nishida, 1982. A new efficient and stereoselective synthesis of Ubiquinone-10. Bull. Chem. Soc. Jap., 55: 1325. DOI: 10.1246/bcsj.55.1325
    • (1982) Bull. Chem. Soc. Jap , vol.55 , pp. 1325
    • Fujita, Y.1    Ishiguro, M.2    Onishi, T.3    Nishida, T.4
  • 18
    • 0021682460 scopus 로고
    • Synthetic studies on isoprenoidquinones. 1. A facile region and streo controlled synthesis of protected hydroquinones with an omegahydroxyprenyl or omega-hydroxygeranyl side chain
    • Masaki, Y., K. Hashimoto and K. Kaji, 1984. Synthetic studies on isoprenoidquinones. 1. A facile region and streo controlled synthesis of protected hydroquinones with an omegahydroxyprenyl or omega-hydroxygeranyl side chain. Chem. Pharm. Bull., 32: 3959. http://www.journalarchive.jst.go.jp/english/ jnlabstract_en.php?cdjournal=cpb1958&cdvol=32&noissue= 10&startpage=3959
    • (1984) Chem. Pharm. Bull , vol.32 , pp. 3959
    • Masaki, Y.1    Hashimoto, K.2    Kaji, K.3
  • 19
    • 85011249866 scopus 로고
    • Synthetic studies on isoprenoidquinones. II. Syntheses of Ubiquinone-10, phylloquinone,and Menaquinone-4 by a chain-extending method utilizing terminally functionalized isoprenoidhydroquinones
    • Masaki, Y., K. Hashimoto, K. Sakuma and K. Kaji, 1984. Synthetic studies on isoprenoidquinones. II. Syntheses of Ubiquinone-10, phylloquinone,and Menaquinone-4 by a chain-extending method utilizing terminally functionalized isoprenoidhydroquinones. Chem. Pharm. Bull., 32: 3952. http://www.journalarchive.jst.go.jp/english/ jnlabstract_en.php?cdjournal=cpb1958&cdvol= 32&noissue=10&startpage=3952
    • (1984) Chem. Pharm. Bull , vol.32 , pp. 3952
    • Masaki, Y.1    Hashimoto, K.2    Sakuma, K.3    Kaji, K.4
  • 20
    • 0002131055 scopus 로고
    • Palladium-catalyzed region and streoselective reduction of allylic compounds with LiBEt3. Application to the synthesis of Co-enzyme Q10
    • DOI: 10.1246/cl.1986.1177
    • Mohri, M., H. Kinoshita, K. Inomata, H. Kotake, H. Takagaki and K. Yamazaki, 1986. Palladium-catalyzed region and streoselective reduction of allylic compounds with LiBEt3. Application to the synthesis of Co-enzyme Q10. Chem. Lett., 15: 1177-1180. DOI: 10.1246/cl.1986.1177
    • (1986) Chem. Lett , vol.15 , pp. 1177-1180
    • Mohri, M.1    Kinoshita, H.2    Inomata, K.3    Kotake, H.4    Takagaki, H.5    Yamazaki, K.6
  • 21
    • 0037021499 scopus 로고    scopus 로고
    • A short, highly efficient synthesis of coenzyme Q10
    • DOI: 10.1021/ja021015v
    • Lipshutz, B.H., P. Mollard, S.S. Pfeiffer and W. Chrisman, 2002. A short, highly efficient synthesis of coenzyme Q10. J. Am. Chem. Soc., 124: 14282-14283. DOI: 10.1021/ja021015v
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 14282-14283
    • Lipshutz, B.H.1    Mollard, P.2    Pfeiffer, S.S.3    Chrisman, W.4
  • 22
    • 0141653948 scopus 로고    scopus 로고
    • The friedel-Crafts allylation of a prenyl group stabilized by a sulfonemoiety: Expeditious syntheses of ubiquinones and menaquinones
    • DOI: 10.1021/jo0350155
    • Min, J.H., J.S. Lee, J.D. Yang and S. Koo, 2003. The friedel-Crafts allylation of a prenyl group stabilized by a sulfonemoiety: Expeditious syntheses of ubiquinones and menaquinones. J. Org. Chem., 68: 7925-7927. DOI: 10.1021/jo0350155
    • (2003) J. Org. Chem , vol.68 , pp. 7925-7927
    • Min, J.H.1    Lee, J.S.2    Yang, J.D.3    Koo, S.4
  • 23
    • 0000333384 scopus 로고
    • Total synthesis of linear polyprenoids. 3. Syntheses of ubiquinones via palladium-catalyzed oligomerization of monoterpene monomers
    • DOI: 10.1021/ ja00221a040
    • Eren, D. and E. Keinan, 1988. Total synthesis of linear polyprenoids. 3. Syntheses of ubiquinones via palladium-catalyzed oligomerization of monoterpene monomers. J. Am. Chem. Soc., 110: 4356-4362. DOI: 10.1021/ ja00221a040
    • (1988) J. Am. Chem. Soc , vol.110 , pp. 4356-4362
    • Eren, D.1    Keinan, E.2
  • 24
    • 8844232972 scopus 로고
    • Total synthesis of polyprenoid natural products via pd(0)-catalyzed oligomerizations
    • Keinan, E. and D. Eren, 1988. Total synthesis of polyprenoid natural products via pd(0)-catalyzed oligomerizations. Pure Applied Chem., 60: 89-98. http://media.iupac.org/publications/pac/1988/pdf/6001x0089.pdf
    • (1988) Pure Applied Chem , vol.60 , pp. 89-98
    • Keinan, E.1    Eren, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.