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Volumn 19, Issue 14, 2008, Pages 1730-1743

Microwave-assisted domino reactions: function-compatibility, modulation, and greening efforts

Author keywords

[No Author keywords available]

Indexed keywords

SOLVENT;

EID: 48349146350     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2008.06.026     Document Type: Article
Times cited : (9)

References (43)
  • 4
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    • Tietze L.F., Brasche G., and Gericke K.M. (Eds), Wiley-VCH, Weinheim, Germany ISBN:3-527-29060-5
    • In: Tietze L.F., Brasche G., and Gericke K.M. (Eds). Domino Reactions in Organic Synthesis (2006), Wiley-VCH, Weinheim, Germany ISBN:3-527-29060-5
    • (2006) Domino Reactions in Organic Synthesis
  • 5
    • 33749241500 scopus 로고    scopus 로고
    • The probe used is an unsaturated bicyclic 1,2-diol having a variable substitution pattern. Advantages are the very rapid increase in molecular complexity and its modular character.
    • The probe used is an unsaturated bicyclic 1,2-diol having a variable substitution pattern. Advantages are the very rapid increase in molecular complexity and its modular character. Safir I., Castellote I., Porcel S., Kaoudi T., Birlirakis N., Toupet L., and Arseniyadis S. Chem. Eur. J. 12 (2006) 7337-7344
    • (2006) Chem. Eur. J. , vol.12 , pp. 7337-7344
    • Safir, I.1    Castellote, I.2    Porcel, S.3    Kaoudi, T.4    Birlirakis, N.5    Toupet, L.6    Arseniyadis, S.7
  • 17
    • 0001520407 scopus 로고
    • Articles dealing with specific aspects of organo lead chemistry:. Wiberg K.B. (Ed), Academic Press, New York Part A
    • Articles dealing with specific aspects of organo lead chemistry:. Criegee R. In: Wiberg K.B. (Ed). Oxidation in Organic Chemistry (1965), Academic Press, New York 277-366 Part A
    • (1965) Oxidation in Organic Chemistry , pp. 277-366
    • Criegee, R.1
  • 18
    • 48349131256 scopus 로고
    • Trahanovsky W.H. (Ed), Academic Press, London Chapter 1
    • Rubottom G.M. In: Trahanovsky W.H. (Ed). Oxidation in Organic Chemistry Vol. D (1982), Academic Press, London Chapter 1
    • (1982) Oxidation in Organic Chemistry , vol.D
    • Rubottom, G.M.1
  • 23
    • 48349116925 scopus 로고    scopus 로고
    • note
    • Taxoid numbering for 3a, Marner's Iridal numbering for 3b and norsesquiterpenespirolactone numbering for 9 is used.
  • 28
    • 48349103259 scopus 로고    scopus 로고
    • note
    • It should be noted that all domino reactions are performed on crude diastereomeric mixtures; we only show the stereopure target diols for characterization purposes, by separating various amounts of stereopure compounds using the eluent indicated in Section 4.
  • 29
    • 48349114198 scopus 로고    scopus 로고
    • note
    • Beilstein numbering is given for the compounds in Section 4, while an easier to follow, though an arbitrary numbering illustrated in Scheme 1 is used in the text.
  • 31
    • 0030013187 scopus 로고    scopus 로고
    • 3 catalyzed double bond migration we adapted the method of
    • 3 catalyzed double bond migration we adapted the method of. Hanselmann R., and Benn M. Synth. Commun. 26 (1996) 945-961
    • (1996) Synth. Commun. , vol.26 , pp. 945-961
    • Hanselmann, R.1    Benn, M.2
  • 36
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    • 2+ but without the toxic and environmental issues:
    • 2+ but without the toxic and environmental issues:. Moriarty R.M., and Vaid R.K. Synthesis (1990) 431-447
    • (1990) Synthesis , pp. 431-447
    • Moriarty, R.M.1    Vaid, R.K.2
  • 42
    • 48349104957 scopus 로고    scopus 로고
    • note
    • By analogy to the higher homologue series, see Ref. 4b.
  • 43
    • 0031027260 scopus 로고    scopus 로고
    • 2 is given as 55 kcal/mol, while the C-Pb bond (2.29 Å) was calculated as 31 kcal/mol
    • 2 is given as 55 kcal/mol, while the C-Pb bond (2.29 Å) was calculated as 31 kcal/mol. Varvoglis A. Tetrahedron 53 (1997) 1179-1255
    • (1997) Tetrahedron , vol.53 , pp. 1179-1255
    • Varvoglis, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.