메뉴 건너뛰기




Volumn 13, Issue 2, 2011, Pages 307-313

Ruthenium(IV) catalysts for the selective estragole to trans-anethole isomerization in environmentally friendly media

Author keywords

[No Author keywords available]

Indexed keywords


EID: 79751482501     PISSN: 14639262     EISSN: 14639270     Source Type: Journal    
DOI: 10.1039/c0gc00417k     Document Type: Article
Times cited : (49)

References (104)
  • 1
    • 36849061264 scopus 로고    scopus 로고
    • See, for example: G. P. Chiusoli and P. M. Maitlis, RSC Publishing, Cambridge
    • See, for example: Metal-Catalysis in Industrial Organic Processes, ed. G. P. Chiusoli and P. M. Maitlis, RSC Publishing, Cambridge, 2008.
    • (2008) Metal-Catalysis in Industrial Organic Processes
  • 6
    • 0004201811 scopus 로고    scopus 로고
    • Aspen Publishers, Maryland, 3rd edn
    • P. R. Ashurst, in Food Flavorings, Aspen Publishers, Maryland, 3rd edn, 1999.
    • (1999) Food Flavorings
    • Ashurst, P.R.1
  • 7
    • 0012680453 scopus 로고
    • B. M. Lawrence, B. D. Mookherjee and B. J. Willis, Elsevier Science Publishers, Amsterdam
    • A. J. Chalk, in Flavors and Fragrances: A World Perspective, ed. B. M. Lawrence, B. D. Mookherjee and B. J. Willis, Elsevier Science Publishers, Amsterdam, 1988.
    • (1988) Flavors and Fragrances: A World Perspective
    • Chalk, A.J.1
  • 9
    • 77952170903 scopus 로고    scopus 로고
    • See also the following report: submitted by the Flavor and Fragrance High Production Volume Consortia (FFHPVC) to the United States Environmental Protection Agency (EPA) in, Available on-line at, accessed July 26, 2010
    • See also the following report: “Test Plan for Estragole” submitted by the Flavor and Fragrance High Production Volume Consortia (FFHPVC) to the United States Environmental Protection Agency (EPA) in 2002. Available on-line at http://www.epa.gov/hpv/pubs/summaries/estragole/c14022tc.htm (accessed July 26, 2010).
    • (2002) Test Plan for Estragole
  • 10
    • 85032778107 scopus 로고
    • Other routes for the large-scale synthesis of anethole, involving the treatment of anisole with propionic acid derivatives or propionaldehyde, are known: SU 261380
    • Other routes for the large-scale synthesis of anethole, involving the treatment of anisole with propionic acid derivatives or propionaldehyde, are known: G. E. Svadkowskaya, L. A. Kheifits, A. I. Platova and K. Denisenlova, USSR Patent, SU 261380, 1970.
    • (1970) USSR Patent
    • Svadkowskaya, G.E.1    Kheifits, L.A.2    Platova, A.I.3    Denisenlova, K.4
  • 12
    • 33644558022 scopus 로고    scopus 로고
    • Anethole formation can also be achieved through different C–C coupling and reduction reactions. However, these methods are not economically viable alternatives for its large-scale production. See, for example
    • Anethole formation can also be achieved through different C–C coupling and reduction reactions. However, these methods are not economically viable alternatives for its large-scale production. See, for example: J. C. Roberts J. A. Pincock J. Org. Chem. 2006 71 1480.
    • (2006) J. Org. Chem. , vol.71 , pp. 1480
    • Roberts, J.C.1    Pincock, J.A.2
  • 20
    • 34548675181 scopus 로고    scopus 로고
    • Anethole is also a principal constituent of other essential oils derived from medicinal plants with anti-oxidant, anti-inflammatory, gastroprotective, psycholeptic and anaesthetic properties: and references cited therein
    • Anethole is also a principal constituent of other essential oils derived from medicinal plants with anti-oxidant, anti-inflammatory, gastroprotective, psycholeptic and anaesthetic properties: P. M. G. Soares R. F. Lima A. de Freitas Pires E. P. Souza A. M. S. Assreuy D. N. Criddle Life Sci. 2007 81 1085 and references cited therein.
    • (2007) Life Sci. , vol.81 , pp. 1085
    • Soares, P.M.G.1    Lima, R.F.2    de Freitas Pires, A.3    Souza, E.P.4    Assreuy, A.M.S.5    Criddle, D.N.6
  • 21
    • 84869156369 scopus 로고    scopus 로고
    • See, for example: US 2009035229
    • See, for example: G. H. Eirew, U.S. Pat., Appl., US 2009035229, 2009.
    • (2009) U.S. Pat., Appl.
    • Eirew, G.H.1
  • 28
    • 85032762390 scopus 로고    scopus 로고
    • Some data on anethole production and consumption can be found in the report: submitted by FFHPVC to EPA, accessed July 26, 2010
    • Some data on anethole production and consumption can be found in the report: “Test Plan for Anethole” submitted by FFHPVC to EPA (http://www.epa.gov/hpv/pubs/summaries/anethole/c14069tc.htm; accessed July 26, 2010).
    • Test Plan for Anethole
  • 31
    • 85032780951 scopus 로고
    • Crystallization at low temperature can also be used to purify trans-anethole, US 4902850
    • Crystallization at low temperature can also be used to purify trans-anethole: C. B. Davies, U.S. Pat. Appl., US 4902850, 1990.
    • (1990) U.S. Pat. Appl.
    • Davies, C.B.1
  • 36
    • 85032759973 scopus 로고    scopus 로고
    • Available on-line at, (accessed July 26, 2010)
    • Available on-line at http://www.fao.org/ag/agn/jecfa-flav (accessed July 26, 2010).
  • 53
    • 0012219553 scopus 로고    scopus 로고
    • J. H. Clark and D. J. Macquarrie, Blackwell Publishing, Abingdon
    • Handbook of Green Chemistry and Technology, ed. J. H. Clark and D. J. Macquarrie, Blackwell Publishing, Abingdon, 2002.
    • (2002) Handbook of Green Chemistry and Technology
  • 70
    • 77954592787 scopus 로고    scopus 로고
    • For a specific review on the use of glycerol as a green solvent, see
    • For a specific review on the use of glycerol as a green solvent, see: Y. Gu F. Jérôme Green Chem. 2010 12 1127.
    • (2010) Green Chem. , vol.12 , pp. 1127
    • Gu, Y.1    Jérôme, F.2
  • 78
    • 31944452612 scopus 로고    scopus 로고
    • Available from Strem Chemicals, Inc (catalog number 44-0203 and 44-0172, respectively). For a review on the coordination chemistry and catalytic applications of these complexes, see
    • Available from Strem Chemicals, Inc (catalog number 44-0203 and 44-0172, respectively). For a review on the coordination chemistry and catalytic applications of these complexes, see: V. Cadierno P. Crochet S. E. García-Garrido J. Gimeno Curr. Org. Chem. 2006 10 165.
    • (2006) Curr. Org. Chem. , vol.10 , pp. 165
    • Cadierno, V.1    Crochet, P.2    García-Garrido, S.E.3    Gimeno, J.4
  • 86
    • 85032767041 scopus 로고    scopus 로고
    • DFT calculations on the relative stability of the E and Z isomers of different 1-propenyl-benzenes have been recently performed by Strukul and co-workers (see ref. 16h). The calculations clearly indicate that the relative stability of the E vs. Z isomers increases with temperature
    • DFT calculations on the relative stability of the E and Z isomers of different 1-propenyl-benzenes have been recently performed by Strukul and co-workers (see ref. 16h). The calculations clearly indicate that the relative stability of the E vs. Z isomers increases with temperature.
  • 87
    • 34447097175 scopus 로고    scopus 로고
    • The combined use of MW-irradiation, as a nonclassical low-energy-consuming heating source, and water, as an environmentally friendly solvent, to perform organic reactions has recently emerged as a promising new field of research. For reviews and a recent book on this topic, see
    • The combined use of MW-irradiation, as a nonclassical low-energy-consuming heating source, and water, as an environmentally friendly solvent, to perform organic reactions has recently emerged as a promising new field of research. For reviews and a recent book on this topic, see: D. Dallinger C. O. Kappe Chem. Rev. 2007 107 2563.
    • (2007) Chem. Rev. , vol.107 , pp. 2563
    • Dallinger, D.1    Kappe, C.O.2
  • 90
    • 79952833483 scopus 로고    scopus 로고
    • V. Polshettiwar and R. S. Varma, RSC Publishing, Cambridge
    • Aqueous Microwave Assisted Chemistry, ed. V. Polshettiwar and R. S. Varma, RSC Publishing, Cambridge, 2010.
    • (2010) Aqueous Microwave Assisted Chemistry
  • 91
    • 85032760593 scopus 로고    scopus 로고
    • 3,7]decane chloride; DAPTA = 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane
    • 3,7]decane chloride; DAPTA = 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane.
  • 92
    • 85032758854 scopus 로고    scopus 로고
    • This happens for example when the poorly soluble dimer 3 is used as catalyst
    • This happens for example when the poorly soluble dimer 3 is used as catalyst.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.